Links to Exploration step
Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">Baff Binds to the Tumor Necrosis Factor Receptor–Like Molecule B Cell Maturation Antigen and Is Important for Maintaining the Peripheral B Cell Population</title><author><name sortKey="Thompson, Jeffrey S" sort="Thompson, Jeffrey S" uniqKey="Thompson J" first="Jeffrey S." last="Thompson">Jeffrey S. Thompson</name><affiliation><nlm:aff id="a">Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Schneider, Pascal" sort="Schneider, Pascal" uniqKey="Schneider P" first="Pascal" last="Schneider">Pascal Schneider</name><affiliation><nlm:aff id="d">Institute of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Kalled, Susan L" sort="Kalled, Susan L" uniqKey="Kalled S" first="Susan L." last="Kalled">Susan L. Kalled</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Wang, Lichun" sort="Wang, Lichun" uniqKey="Wang L" first="Lichun" last="Wang">Lichun Wang</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Lefevre, Eric A" sort="Lefevre, Eric A" uniqKey="Lefevre E" first="Eric A." last="Lefevre">Eric A. Lefevre</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Cachero, Teresa G" sort="Cachero, Teresa G" uniqKey="Cachero T" first="Teresa G." last="Cachero">Teresa G. Cachero</name><affiliation><nlm:aff id="c">Department of Protein Engineering, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Mackay, Fabienne" sort="Mackay, Fabienne" uniqKey="Mackay F" first="Fabienne" last="Mackay">Fabienne Mackay</name><affiliation><nlm:aff id="f">Garvan Institute of Medical Research, St. Vincent's Hospital, Darlinghurst NSW 2010, Australia</nlm:aff></affiliation></author><author><name sortKey="Bixler, Sarah A" sort="Bixler, Sarah A" uniqKey="Bixler S" first="Sarah A." last="Bixler">Sarah A. Bixler</name><affiliation><nlm:aff id="a">Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Zafari, Mohammad" sort="Zafari, Mohammad" uniqKey="Zafari M" first="Mohammad" last="Zafari">Mohammad Zafari</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Liu, Zhong Ying" sort="Liu, Zhong Ying" uniqKey="Liu Z" first="Zhong-Ying" last="Liu">Zhong-Ying Liu</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Woodcock, Stephen A" sort="Woodcock, Stephen A" uniqKey="Woodcock S" first="Stephen A." last="Woodcock">Stephen A. Woodcock</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Qian, Fang" sort="Qian, Fang" uniqKey="Qian F" first="Fang" last="Qian">Fang Qian</name><affiliation><nlm:aff id="c">Department of Protein Engineering, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Batten, Marcel" sort="Batten, Marcel" uniqKey="Batten M" first="Marcel" last="Batten">Marcel Batten</name><affiliation><nlm:aff id="f">Garvan Institute of Medical Research, St. Vincent's Hospital, Darlinghurst NSW 2010, Australia</nlm:aff></affiliation></author><author><name sortKey="Madry, Christine" sort="Madry, Christine" uniqKey="Madry C" first="Christine" last="Madry">Christine Madry</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Richard, Yolande" sort="Richard, Yolande" uniqKey="Richard Y" first="Yolande" last="Richard">Yolande Richard</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Benjamin, Christopher D" sort="Benjamin, Christopher D" uniqKey="Benjamin C" first="Christopher D." last="Benjamin">Christopher D. Benjamin</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Browning, Jeffrey L" sort="Browning, Jeffrey L" uniqKey="Browning J" first="Jeffrey L." last="Browning">Jeffrey L. Browning</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Tsapis, Andreas" sort="Tsapis, Andreas" uniqKey="Tsapis A" first="Andreas" last="Tsapis">Andreas Tsapis</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Tschopp, Jurg" sort="Tschopp, Jurg" uniqKey="Tschopp J" first="Jurg" last="Tschopp">Jurg Tschopp</name><affiliation><nlm:aff id="d">Institute of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Ambrose, Christine" sort="Ambrose, Christine" uniqKey="Ambrose C" first="Christine" last="Ambrose">Christine Ambrose</name><affiliation><nlm:aff id="a">Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">10880534</idno><idno type="pmc">1887706</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1887706</idno><idno type="RBID">PMC:1887706</idno><date when="2000">2000</date><idno type="wicri:Area/Pmc/Corpus">001125</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">001125</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Baff Binds to the Tumor Necrosis Factor Receptor–Like Molecule B Cell Maturation Antigen and Is Important for Maintaining the Peripheral B Cell Population</title><author><name sortKey="Thompson, Jeffrey S" sort="Thompson, Jeffrey S" uniqKey="Thompson J" first="Jeffrey S." last="Thompson">Jeffrey S. Thompson</name><affiliation><nlm:aff id="a">Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Schneider, Pascal" sort="Schneider, Pascal" uniqKey="Schneider P" first="Pascal" last="Schneider">Pascal Schneider</name><affiliation><nlm:aff id="d">Institute of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Kalled, Susan L" sort="Kalled, Susan L" uniqKey="Kalled S" first="Susan L." last="Kalled">Susan L. Kalled</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Wang, Lichun" sort="Wang, Lichun" uniqKey="Wang L" first="Lichun" last="Wang">Lichun Wang</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Lefevre, Eric A" sort="Lefevre, Eric A" uniqKey="Lefevre E" first="Eric A." last="Lefevre">Eric A. Lefevre</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Cachero, Teresa G" sort="Cachero, Teresa G" uniqKey="Cachero T" first="Teresa G." last="Cachero">Teresa G. Cachero</name><affiliation><nlm:aff id="c">Department of Protein Engineering, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Mackay, Fabienne" sort="Mackay, Fabienne" uniqKey="Mackay F" first="Fabienne" last="Mackay">Fabienne Mackay</name><affiliation><nlm:aff id="f">Garvan Institute of Medical Research, St. Vincent's Hospital, Darlinghurst NSW 2010, Australia</nlm:aff></affiliation></author><author><name sortKey="Bixler, Sarah A" sort="Bixler, Sarah A" uniqKey="Bixler S" first="Sarah A." last="Bixler">Sarah A. Bixler</name><affiliation><nlm:aff id="a">Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Zafari, Mohammad" sort="Zafari, Mohammad" uniqKey="Zafari M" first="Mohammad" last="Zafari">Mohammad Zafari</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Liu, Zhong Ying" sort="Liu, Zhong Ying" uniqKey="Liu Z" first="Zhong-Ying" last="Liu">Zhong-Ying Liu</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Woodcock, Stephen A" sort="Woodcock, Stephen A" uniqKey="Woodcock S" first="Stephen A." last="Woodcock">Stephen A. Woodcock</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Qian, Fang" sort="Qian, Fang" uniqKey="Qian F" first="Fang" last="Qian">Fang Qian</name><affiliation><nlm:aff id="c">Department of Protein Engineering, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Batten, Marcel" sort="Batten, Marcel" uniqKey="Batten M" first="Marcel" last="Batten">Marcel Batten</name><affiliation><nlm:aff id="f">Garvan Institute of Medical Research, St. Vincent's Hospital, Darlinghurst NSW 2010, Australia</nlm:aff></affiliation></author><author><name sortKey="Madry, Christine" sort="Madry, Christine" uniqKey="Madry C" first="Christine" last="Madry">Christine Madry</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Richard, Yolande" sort="Richard, Yolande" uniqKey="Richard Y" first="Yolande" last="Richard">Yolande Richard</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Benjamin, Christopher D" sort="Benjamin, Christopher D" uniqKey="Benjamin C" first="Christopher D." last="Benjamin">Christopher D. Benjamin</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Browning, Jeffrey L" sort="Browning, Jeffrey L" uniqKey="Browning J" first="Jeffrey L." last="Browning">Jeffrey L. Browning</name><affiliation><nlm:aff id="b">Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author><author><name sortKey="Tsapis, Andreas" sort="Tsapis, Andreas" uniqKey="Tsapis A" first="Andreas" last="Tsapis">Andreas Tsapis</name><affiliation><nlm:aff id="e">Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</nlm:aff></affiliation></author><author><name sortKey="Tschopp, Jurg" sort="Tschopp, Jurg" uniqKey="Tschopp J" first="Jurg" last="Tschopp">Jurg Tschopp</name><affiliation><nlm:aff id="d">Institute of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland</nlm:aff></affiliation></author><author><name sortKey="Ambrose, Christine" sort="Ambrose, Christine" uniqKey="Ambrose C" first="Christine" last="Ambrose">Christine Ambrose</name><affiliation><nlm:aff id="a">Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142</nlm:aff></affiliation></author></analytic><series><title level="j">The Journal of Experimental Medicine</title><idno type="ISSN">0022-1007</idno><idno type="eISSN">1540-9538</idno><imprint><date when="2000">2000</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>The tumor necrosis factor (TNF) family member B cell activating factor (BAFF) binds B cells and enhances B cell receptor–triggered proliferation. We find that B cell maturation antigen (BCMA), a predicted member of the TNF receptor family expressed primarily in mature B cells, is a receptor for BAFF. Although BCMA was previously localized to the Golgi apparatus, BCMA was found to be expressed on the surface of transfected cells and tonsillar B cells. A soluble form of BCMA, which inhibited the binding of BAFF to a B cell line, induced a dramatic decrease in the number of peripheral B cells when administered in vivo. Moreover, culturing splenic cells in the presence of BAFF increased survival of a percentage of the B cells. These results are consistent with a role for BAFF in maintaining homeostasis of the B cell population.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct><biblStruct></biblStruct></listBibl></div1></back></TEI><pmc article-type="research-article"><pmc-dir>properties open_access</pmc-dir>
<front><journal-meta><journal-id journal-id-type="nlm-ta">J Exp Med</journal-id><journal-title>The Journal of Experimental Medicine</journal-title><issn pub-type="ppub">0022-1007</issn><issn pub-type="epub">1540-9538</issn><publisher><publisher-name>The Rockefeller University Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">10880534</article-id><article-id pub-id-type="pmc">1887706</article-id><article-id pub-id-type="publisher-id">000648</article-id><article-categories><subj-group subj-group-type="heading"><subject>Brief Definitive Reports</subject></subj-group></article-categories><title-group><article-title>Baff Binds to the Tumor Necrosis Factor Receptor–Like Molecule B Cell Maturation Antigen and Is Important for Maintaining the Peripheral B Cell Population</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Thompson</surname><given-names>Jeffrey S.</given-names></name><xref ref-type="aff" rid="a">a</xref></contrib><contrib contrib-type="author"><name><surname>Schneider</surname><given-names>Pascal</given-names></name><xref ref-type="aff" rid="d">d</xref></contrib><contrib contrib-type="author"><name><surname>Kalled</surname><given-names>Susan L.</given-names></name><xref ref-type="aff" rid="b">b</xref></contrib><contrib contrib-type="author"><name><surname>Wang</surname><given-names>LiChun</given-names></name><xref ref-type="aff" rid="b">b</xref></contrib><contrib contrib-type="author"><name><surname>Lefevre</surname><given-names>Eric A.</given-names></name><xref ref-type="aff" rid="e">e</xref></contrib><contrib contrib-type="author"><name><surname>Cachero</surname><given-names>Teresa G.</given-names></name><xref ref-type="aff" rid="c">c</xref></contrib><contrib contrib-type="author"><name><surname>MacKay</surname><given-names>Fabienne</given-names></name><xref ref-type="aff" rid="f">f</xref></contrib><contrib contrib-type="author"><name><surname>Bixler</surname><given-names>Sarah A.</given-names></name><xref ref-type="aff" rid="a">a</xref></contrib><contrib contrib-type="author"><name><surname>Zafari</surname><given-names>Mohammad</given-names></name><xref ref-type="aff" rid="b">b</xref></contrib><contrib contrib-type="author"><name><surname>Liu</surname><given-names>Zhong-Ying</given-names></name><xref ref-type="aff" rid="b">b</xref></contrib><contrib contrib-type="author"><name><surname>Woodcock</surname><given-names>Stephen A.</given-names></name><xref ref-type="aff" rid="b">b</xref></contrib><contrib contrib-type="author"><name><surname>Qian</surname><given-names>Fang</given-names></name><xref ref-type="aff" rid="c">c</xref></contrib><contrib contrib-type="author"><name><surname>Batten</surname><given-names>Marcel</given-names></name><xref ref-type="aff" rid="f">f</xref></contrib><contrib contrib-type="author"><name><surname>Madry</surname><given-names>Christine</given-names></name><xref ref-type="aff" rid="e">e</xref></contrib><contrib contrib-type="author"><name><surname>Richard</surname><given-names>Yolande</given-names></name><xref ref-type="aff" rid="e">e</xref></contrib><contrib contrib-type="author"><name><surname>Benjamin</surname><given-names>Christopher D.</given-names></name><xref ref-type="aff" rid="b">b</xref></contrib><contrib contrib-type="author"><name><surname>Browning</surname><given-names>Jeffrey L.</given-names></name><xref ref-type="aff" rid="b">b</xref></contrib><contrib contrib-type="author"><name><surname>Tsapis</surname><given-names>Andreas</given-names></name><xref ref-type="aff" rid="e">e</xref></contrib><contrib contrib-type="author"><name><surname>Tschopp</surname><given-names>Jurg</given-names></name><xref ref-type="aff" rid="d">d</xref></contrib><contrib contrib-type="author"><name><surname>Ambrose</surname><given-names>Christine</given-names></name><address><addr-line>Biogen, Inc., 12 Cambridge Center, Cambridge, MA 02142.</addr-line><fax>617-679-2304</fax><phone>617-679-3340</phone></address><email>christine_ambrose@biogen.com</email><xref ref-type="aff" rid="a">a</xref></contrib><aff id="a"><label>a</label>Department of Molecular Genetics, Biogen, Incorporated, Cambridge, Massachusetts 02142</aff><aff id="b"><label>b</label>Department of Immunology and Inflammation, Biogen, Incorporated, Cambridge, Massachusetts 02142</aff><aff id="c"><label>c</label>Department of Protein Engineering, Biogen, Incorporated, Cambridge, Massachusetts 02142</aff><aff id="d"><label>d</label>Institute of Biochemistry, University of Lausanne, CH-1066 Epalinges, Switzerland</aff><aff id="e"><label>e</label>Institut National de la Santé et de la Recherche Médicale U131, 92140 Clamart, France</aff><aff id="f"><label>f</label>Garvan Institute of Medical Research, St. Vincent's Hospital, Darlinghurst NSW 2010, Australia</aff></contrib-group><pub-date pub-type="ppub"><day>3</day><month>7</month><year>2000</year></pub-date><volume>192</volume><issue>1</issue><fpage>129</fpage><lpage>136</lpage><history><date date-type="received"><day>19</day><month>4</month><year>2000</year></date><date date-type="rev-request"><day>24</day><month>5</month><year>2000</year></date><date date-type="accepted"><day>25</day><month>5</month><year>2000</year></date></history><permissions><copyright-statement>© 2000 The Rockefeller University Press</copyright-statement><copyright-year>2000</copyright-year><copyright-holder>The Rockefeller University Press</copyright-holder></permissions><abstract><p>The tumor necrosis factor (TNF) family member B cell activating factor (BAFF) binds B cells and enhances B cell receptor–triggered proliferation. We find that B cell maturation antigen (BCMA), a predicted member of the TNF receptor family expressed primarily in mature B cells, is a receptor for BAFF. Although BCMA was previously localized to the Golgi apparatus, BCMA was found to be expressed on the surface of transfected cells and tonsillar B cells. A soluble form of BCMA, which inhibited the binding of BAFF to a B cell line, induced a dramatic decrease in the number of peripheral B cells when administered in vivo. Moreover, culturing splenic cells in the presence of BAFF increased survival of a percentage of the B cells. These results are consistent with a role for BAFF in maintaining homeostasis of the B cell population.</p></abstract><kwd-group><kwd>tumor necrosis factor</kwd><kwd>B lymphocyte</kwd><kwd>receptor</kwd><kwd>cell survival</kwd><kwd>homeostasis</kwd></kwd-group></article-meta></front><body><sec><title>Introduction</title><p>Many members of the TNF family fulfill important roles related to the organization, function, and/or homeostasis of the immune system <xref ref-type="bib" rid="R1">1</xref>. The recently identified TNF family member B cell activating factor (BAFF) (TNF and apoptosis ligand–related leukocyte-expressed ligand 1 [TALL-1]/TNF homologue that activates apoptosis, nuclear factor κB, and c-Jun NH<sub>2</sub>-terminal kinase [THANK]/B lymphocyte stimulator [BlyS]; references <xref ref-type="bib" rid="R2">2</xref><xref ref-type="bib" rid="R3">3</xref><xref ref-type="bib" rid="R4">4</xref><xref ref-type="bib" rid="R5">5</xref>) is expressed in monocytes, macrophages, and dendritic cells <xref ref-type="bib" rid="R2">2</xref><xref ref-type="bib" rid="R3">3</xref><xref ref-type="bib" rid="R5">5</xref> and has been shown to bind to B cells and increase the proliferation of B cells in combination with an anti–B cell receptor antibody in vitro <xref ref-type="bib" rid="R2">2</xref><xref ref-type="bib" rid="R5">5</xref>. BAFF is a type II membrane protein and may act as either a membrane-bound or soluble form, the latter being generated by proteolytic cleavage at a furin consensus site <xref ref-type="bib" rid="R2">2</xref><xref ref-type="bib" rid="R5">5</xref>. Transgenic mice overexpressing BAFF have a greatly elevated number of mature B cells and an increased number of effector T cells in their spleen and mesenteric lymph nodes <xref ref-type="bib" rid="R6">6</xref>. These mice display autoimmune-like manifestations including high levels of rheumatoid factors, circulating immune complexes, anti-DNA autoantibodies, and Ig deposition in the kidney <xref ref-type="bib" rid="R6">6</xref>. However, splenic B cells from transgenic or control mice were found to proliferate at the same rate <xref ref-type="bib" rid="R6">6</xref>, suggesting that BAFF, in addition to its ability to costimulate B cell proliferation in vitro, may have alternative functions.</p><p>B cell maturation antigen (BCMA) was first identified as part of a translocation event in a malignant T cell lymphoma patient <xref ref-type="bib" rid="R7">7</xref>. Characterization of human BCMA identified it as a type I membrane protein primarily expressed in immune organs and mature B cell lines <xref ref-type="bib" rid="R7">7</xref><xref ref-type="bib" rid="R8">8</xref>. BCMA protein was localized to the Golgi apparatus in the U266 plasmacytoma cell line, which expresses high levels of BCMA <xref ref-type="bib" rid="R9">9</xref>. Subsequent identification of the mouse BCMA gene and further motif analysis led to the prediction that BCMA is a member of the TNF receptor superfamily <xref ref-type="bib" rid="R10">10</xref>.</p><p>Here, we show that BAFF is capable of interacting with the orphan TNF receptor, BCMA. We characterize the BAFF–BCMA interaction and show that injection of soluble BCMA-Ig fusion protein into mice leads to a dramatic reduction in the total number of B cells in the peripheral immune organs. This may be due to a B cell survival function of BAFF. Modulation of the peripheral B cell population using BCMA-Ig treatment may be efficacious in treating B cell–mediated disorders.</p></sec><sec sec-type="materials|methods"><title>Materials and Methods</title><sec><title>Cells and Constructs.</title><p>Human embryonic 293 cells carrying the EBNA-1 gene were cultured in DMEM plus 10% FCS, glutamine, pen-strep, and 250 μg/ml G418. Raji cells were obtained from American Type Culture Collection and were cultured as indicated. The human BCMA-hIgG1 (BCMA-Ig) expression vector was created using a murine κ light chain signal sequence, a PCR fragment generated to BCMA amino acids 1–48 (second Met), and a hIgG1 SalI + NotI fragment <xref ref-type="bib" rid="R11">11</xref>. The fragments were cloned into pCEP4 (Invitrogen) derivative. A COOH-terminal 6×His-tagged full-length human BCMA expression vector was generated by PCR. BCMA-Ig obtained by transient transfection of 293E cells using Lipofectamine (Life Technologies) was purified by protein A column chromatography, and contained <1 endotoxin U/mg of protein. The half-life of this protein in mice is ∼3.5 d. The control Ig, nonbinding LFA3-Ig, was prepared from a Chinese hamster ovary (CHO) cell line as described <xref ref-type="bib" rid="R12">12</xref>. Murine lymphotoxin (LT)βR-Ig <xref ref-type="bib" rid="R13">13</xref> and human LTβR-Ig <xref ref-type="bib" rid="R14">14</xref> were made as described. Receptor-Ig fusion proteins and Flag-tagged soluble ligands were constructed and expressed as described using the following amino acid sequences: hTNF-α (85–263), mBAFF (127–309), hBAFF (136–285 or 83–285), human receptor activator of nuclear factor κB ligand (hRANKL [151–316]), hCD30L (63–234), hCD40L (116–261), homologous to lymphotoxins, exhibits inducible expression, and competes with HSV glycoprotein D for herpesvirus entry mediator (HVEM), a receptor expressed by T lymphocytes (hLIGHT [89–240]), hTNFR2 (1–257), hTNF-related apoptosis-inducing ligand (hTRAIL)R2 (1–212), hCD30 (1–380), hCD40 (1–193), hHVEM (1–200), and mRANK (1–200) <xref ref-type="bib" rid="R2">2</xref><xref ref-type="bib" rid="R15">15</xref>. Unless indicated, BAFF in 15-fold concentrated serum-free Optimem medium (Life Technologies) was used <xref ref-type="bib" rid="R2">2</xref>.</p></sec><sec><title>Anti-BCMA Antibodies.</title><p>Rabbit anti-hBCMA antibody, Rb 1593, was generated against purified hBCMA-Ig. Affinity-purified anti-BCMA antibodies and control affinity-purified anti–glutathione <italic>S</italic>-transferase (GST) antibodies originating from the same rabbit were used for the U266 cells and tonsillar B cell staining. These antibodies have been described <xref ref-type="bib" rid="R9">9</xref>.</p></sec><sec><title>BIAcore Analysis.</title><p>All experiments were performed at 25°C with a 10 μl/min flow rate using a BIAcore 2000™. HBS buffer (10 mM Hepes, 150 mM NaCl, 0.005% P20 surfactant, pH 7.4) was used both as the running buffer and as the sample diluent. The CM5 chip (BIAcore) surface was first activated with <italic>N</italic>-hydroxysuccinimide/N-ethyl-N9-(3-diethylaminopropyl)-carbodiimide hydrochloride. 25 μl of BCMA-Ig or hLTβR-Ig was diluted to 30 μg/ml in 10 mM acetic acid (pH 5), then injected. The unreacted groups of the chip's dextran matrix were blocked twice with ethanolamine-HCl (pH 8.5). For the experiment, 100 μl of Flag-hBAFF, Flag-mBAFF, or hLTα<sub>1</sub>β<sub>2</sub> at 30 μg/ml in diluent buffer were injected over the surface of the chip. The surface was regenerated between experiments by washing with 1 mM formic acid.</p></sec><sec><title>BCMA-Ig Blocking of BAFF Binding to Raji Cells.</title><p>Flag-tagged human BAFF at 200 ng/ml was pre-incubated for 30 min on ice in FACS<sup>®</sup> buffer (PBS, 10% FCS, 0.05% azide) with either hBCMA-Ig or hLTβR-Ig at twofold dilutions ranging from 20 μg/ml to 39 ng/ml, or with BAFF alone. The mixture was added to Raji cells for 30 min on ice. Bound BAFF was detected using 5 μg/ml anti-Flag antibody M2 (Sigma-Aldrich) followed by PE-conjugated donkey anti–mouse IgG (Jackson ImmunoResearch Laboratories). The samples were read using a FACSCalibur™ flow cytometer (Becton Dickinson).</p></sec><sec><title>Anti-BCMA Antibody and BAFF Binding to Full-length BCMA-transfected Cells.</title><p>293E cells were transfected with either vector alone or His-tagged full-length BCMA and a green fluorescent protein transfection control plasmid (gift of N. Horikoshi, Beth Israel Deaconess Medical Center, Boston, MA) using Lipofectamine 2000. After 48 h, the cells were detached in PBS containing 5 mM EDTA, washed, and stained for 30 min on ice with anti-hBCMA Rb 1593 (1:1,000) or preimmune sera (1:500) followed by PE-conjugated donkey anti–rabbit Ig (1:100; Jackson ImmunoResearch Laboratories). Alternatively, cells were stained plus or minus Flag-BAFF (2 μg/ml) and detected using M2 as described above.</p></sec><sec><title>BAFF and Anti-BCMA Antibody Binding to Human Tonsillar B Cells.</title><p>Human mononuclear cells were obtained from palatine tonsils by gentle dissociation with forceps. T cells were removed by one cycle of rosette formation and further depleted with anti-CD2 magnetic beads (Dynabeads M-450; Dynal <xref ref-type="bib" rid="R16">16</xref>). The remaining B cell populations were 93 ± 4% CD19<sup>+</sup>, 59 ± 6% IgD<sup>+</sup>, 56 ± 5% IgM<sup>+</sup>, 81 ± 16% CD44<sup>+</sup>, 21 ± 6% CD38<sup>+</sup>, 42 ± 1% CD95<sup>+</sup>, and ≤ 1% CD14<sup>+</sup>, CD3<sup>+</sup>, and DRC1<sup>+</sup> cells. Cells were preincubated with 10% human AB serum and stained plus or minus Flag-BAFF (amino acids 83–285) at 1 μg/ml followed by M2 (7.5 μg/ml) and PE-conjugated goat anti–mouse IgG (Immunotech). Anti-BCMA staining was done using 20 μg/ml antibody and FITC-conjugated goat anti–rabbit IgG (Immunotech).</p></sec><sec><title>BCMA-Ig Injection into Mice.</title><p>6-wk-old female BALB/c mice (four per group; The Jackson Laboratory) received intraperitoneal injections of either 400 μg of BCMA-Ig or 400 μg of LFA3-Ig (control Ig) on days 1, 4, 8, and 11. On day 19, the mice were killed. Blood was collected via cardiac puncture into tubes containing EDTA. Single cell suspensions were prepared from spleens and mesenteric lymph nodes, and RBCs were lysed in a hypotonic buffer. Flow cytometry was performed using PE-, FITC-, or CyChrome-conjugated anti-CD45R/B220 (B cells) and anti-CD4, anti-CD8 (T cells), or anti-Gr1/anti–Mac-1 (neutrophils and macrophages). All antibodies were purchased from BD PharMingen. In brief, Fc receptors were blocked with 10 μg/ml FcBlock (BD PharMingen) for 15 min on ice followed by addition of the conjugated mAbs, and were incubated on ice for 30 min. Cells were washed twice, suspended in 0.5% paraformaldehyde, and analyzed by flow cytometry.</p></sec><sec><title>B Cell Survival Assay.</title><p>Mouse spleens were collected under sterile conditions and homogenized in RPMI medium plus 10% FCS using SuperFrost glass slides (Menzel-Glaser). Cells were filtered through a 70-μm nylon cell strainer (Falcon) before centrifugation at 1,000 rpm (300 <italic>g</italic>) for 5 min. The pellet was resuspended in 2 ml/spleen RBC lysis solution and incubated on ice for 5 min. The remaining white blood cells were collected by centrifugation and resuspended in media. Splenocytes were incubated at a concentration of 3 × 10<sup>6</sup> cells/ml in media for 72 h. The splenocytes were either untreated or were in the presence of 2 μg/ml human Flag-BAFF (amino acids 83–285) alone or with 20 μg/ml BCMA-Ig or 20 μg/ml murine LTβR-Ig. The percent live cells remaining was determined using the annexin V–FITC Apoptosis Detection Kit 1 (BD PharMingen). Cells were washed twice and then analyzed using a FACSCalibur™ machine (Becton Dickinson).</p></sec></sec><sec><title>Results and Discussion</title><sec><title>BAFF Interacts with Soluble BCMA.</title><p>TNF receptor family members are generally type I proteins with a leader sequence and a cysteine-rich extracellular domain. The extracellular domains are organized as a series of alternating A and B modules, which are stabilized by internal disulfide bridges <xref ref-type="bib" rid="R17">17</xref>. A single C module, not involved in ligand binding, is found in the fourth cysteine repeat of TNFRI <xref ref-type="bib" rid="R17">17</xref>. In a previous study, BAFF failed to bind to 16 members of the TNF receptor family <xref ref-type="bib" rid="R2">2</xref>. Subsequently, an additional candidate receptor for BAFF was identified, termed B cell maturation antigen <xref ref-type="bib" rid="R10">10</xref>. BCMA appears to be distantly related to the TNF receptor family, because it is devoid of a signal sequence and contains a single A and one C module instead of multiple A and B modules <xref ref-type="bib" rid="R10">10</xref>. However, the expression pattern of this atypical receptor in mature B cells prompted us to examine its interaction with BAFF <xref ref-type="bib" rid="R8">8</xref><xref ref-type="bib" rid="R9">9</xref>. To this end, the extracellular domain of human BCMA was expressed as a human IgG1 fusion protein and was targeted to the secretory pathway with an added signal peptide. BCMA-hIgG1 (BCMA-Ig) fusion protein immunoprecipitated both recombinant human and murine BAFF very efficiently, but not five other TNF ligands (CD40L, RANKL, CD30L, LIGHT, and TNF-α) which, however, interacted with their respective receptors in control immunoprecipitations (<xref ref-type="fig" rid="F1">Fig. 1</xref> A). When the interaction was tested in another format using surface plasmon resonance (BIAcore) analysis, similar results were obtained, and both murine and human BAFF exhibited a significant affinity for human BCMA-Ig but not for LTβR-Ig (<xref ref-type="fig" rid="F1">Fig. 1</xref> B). In addition, BCMA-Ig interacted with membrane-bound BAFF expressed in 293 cells (<xref ref-type="fig" rid="F1">Fig. 1</xref> C), and in a dose-dependent manner specifically blocked the interaction of BAFF with Raji B cells (<xref ref-type="fig" rid="F1">Fig. 1</xref> D). Thus, the short extracellular domain of BCMA is sufficient for high-affinity binding to BAFF, and there is no species barrier for the murine BAFF–human BCMA interaction. The BAFF–BCMA interaction is presently unique in the family, as it involves only two modules, one predicted to be of the C type. In the two cases where the crystal structure of the trimeric ligand–receptor complex is known (LTα–TNFR1 and TRAIL–TRAILR2), the contacts involved in the interaction have been shown to involve one B and two A modules <xref ref-type="bib" rid="R18">18</xref><xref ref-type="bib" rid="R19">19</xref><xref ref-type="bib" rid="R20">20</xref>.</p></sec><sec><title>Cell Surface Expression of BCMA.</title><p>Cell surface expression of BCMA is a likely prerequisite for BAFF binding. Indeed, most 293E cells transfected with a construct encoding full-length BCMA with no added signal peptide were positive for surface staining with anti-BCMA antibodies and to a lesser extent with Flag-BAFF, whereas untransfected cells or cells transfected with a control plasmid were not (<xref ref-type="fig" rid="F2">Fig. 2</xref> A). We also found that tonsillar B cells were stained with both anti-BCMA and Flag-BAFF (<xref ref-type="fig" rid="F2">Fig. 2</xref> B), suggesting that surface expression of BCMA also occurs in primary cells and is not an artifact of overexpression. Therefore, in the absence of a signal sequence, the transmembrane domain of BCMA must dictate the topology of membrane insertion for correct expression at the cell surface. In a previous study, BCMA was located exclusively in the Golgi apparatus of the plasmocytic cell line U266, and not at the cell surface, despite the fact that these cells express high levels of the protein <xref ref-type="bib" rid="R9">9</xref>. Consistent with this observation, we find that U266 cells were not stained with either the anti-BCMA antibody or Flag-BAFF (<xref ref-type="fig" rid="F2">Fig. 2</xref> B). These results suggest that surface expression of BCMA may be a tightly controlled, cell type–dependent mechanism. Intracellular pools of the cytotoxic receptor Fas can be mobilized for surface expression in response to p53 activation, a mechanism that probably contributes to the elimination of damaged cells <xref ref-type="bib" rid="R21">21</xref>. It is an intriguing possibility that cells may release intracellular BCMA at the cell surface in response to specific stimuli, and therefore become sensitive to BAFF effects.</p></sec><sec><title>B Cell Reduction with BCMA-Ig Treatment.</title><p>Because BIAcore studies revealed that murine BAFF was able to effectively bind human BCMA-Ig, we used the fusion protein to examine the effect of disrupting the BAFF signal in normal mice. Four administrations of BCMA-Ig at intervals of 3–4 d dramatically reduced the total number of B cells in the blood and peripheral lymphoid organs examined. The B220<sup>+</sup> B cell population in the spleen of BCMA-Ig–treated animals was reduced by 50% compared with the control Ig–treated mice. In contrast, populations of neutrophils, macrophages, CD4<sup>+</sup> T cells, and CD8<sup>+</sup> T cells were not significantly affected by BCMA-Ig (<xref ref-type="fig" rid="F3">Fig. 3</xref> and <xref ref-type="table" rid="T1">Table </xref>). The decrease in absolute B cell number corresponded to the decrease in absolute total cell number (<xref ref-type="table" rid="T1">Table </xref>), indicating that the reduction in the B cell population was not due to a concordant increase in other cell types. Therefore, the BCMA-Ig treatment specifically affected B cells. Similar results were observed in the blood and mesenteric lymph nodes, where approximately half of the B220<sup>+</sup> B cells were lost (data not shown). As B cells do not express BAFF <xref ref-type="bib" rid="R2">2</xref><xref ref-type="bib" rid="R5">5</xref>, and because human BCMA-Ig does not bind to mouse splenic B cells (data not shown), we can exclude antibody-dependent cell-mediated cytotoxicity as the mechanism of action. Although BAFF is thought to be primarily secreted, staining of splenocytes using BCMA-Ig revealed that BAFF is found on the surface of Mac-1<sup>+</sup> cells (data not shown).</p><p>BCMA-Ig treatment given over the course of 11 d may reduce the peripheral B cell pool by inhibiting production or release of immature B cells from the bone marrow, by blocking maturation of immature B cells, or by sequestering a factor required for B cell survival. At least 20 × 10<sup>6</sup> immature B cells are generated in the bone marrow each day, and from this population an estimated 2–3 × 10<sup>6</sup> B cells enter the periphery <xref ref-type="bib" rid="R22">22</xref>. It has been shown that maintenance of the peripheral B cell pool requires a minimum continuous input of newly formed cells <xref ref-type="bib" rid="R23">23</xref>, but that less than half of the B cells that reach the spleen progress to the mature phenotype <xref ref-type="bib" rid="R24">24</xref>. Although the percentage of long-lived and short-lived B cells in the periphery is controversial <xref ref-type="bib" rid="R22">22</xref>, the average half-life of the B220<sup>+</sup> cells in the spleen is 4.3 wk, indicating that the majority of the B cells are long-lived mature cells <xref ref-type="bib" rid="R24">24</xref>. As we see a 50% decrease in the total B cell population in the periphery, we may be affecting the repopulation of the spleen with mature B cells or the survival of the existing mature B cells. One possible mechanism for sustaining B cell survival is to upregulate the antiapoptotic protein Bcl-2. Interestingly, elevated levels of Bcl-2 have been reported in the PBL B cells isolated from BAFF transgenic mice <xref ref-type="bib" rid="R6">6</xref>. To delineate the peripheral B cell subpopulations modulated by BCMA-Ig, the mechanism of action, as well as any potential effect on B cell development in the bone marrow, a more comprehensive study is in progress.</p></sec><sec><title>B Cell Survival with BAFF.</title><p>The in vivo analysis, taken together with the finding that BAFF transgenic mice have an increased number of mature B cells and Bcl-2 expression, indicates that BAFF may promote B cell survival. We next examined the direct effect of BAFF on the survival of murine splenocytes in vitro. Splenocytes were cultured for 72 h in the presence or absence of BAFF and either BCMA-Ig or LTβR-Ig (<xref ref-type="fig" rid="F4">Fig. 4</xref>). BAFF alone caused an increase in the percentage of cells that survived, and this effect was blocked with BCMA-Ig. The increase in cell numbers was not due to the increase in proliferation, as this has not been observed in the absence of B cell receptor stimulation <xref ref-type="bib" rid="R2">2</xref><xref ref-type="bib" rid="R3">3</xref>. The majority of the surviving cells, ∼80%, were B220<sup>+</sup> B cells, although a small percentage of T cells also survived (data not shown). Thus, BAFF is capable of directly enhancing B cell survival.</p><p>In conclusion, we have identified BCMA as a receptor for BAFF. Soluble BCMA antagonizes BAFF action and leads to a rapid, significant B cell decline in vivo, suggesting that BAFF is necessary for homeostasis of the peripheral B cell pool. The increase in mature B cell numbers observed in the BAFF transgenic mice and the ability of BAFF to sustain B cells in vitro indicate that BAFF functions as a survival factor. Modulation of the peripheral B cell population using soluble BCMA may have applications in treating B cell–mediated autoimmune diseases, plasma cell disorders, and B cell cancers. A very recent report has demonstrated that blocking the BAFF pathway in two models of SLE using a soluble version of another receptor for BAFF, transmembrane activator and calcium modulator and cyclophilin ligand (CAML) interactor (TACI)-Ig, eliminates proteinurea and prolongs the life span of the mice <xref ref-type="bib" rid="R25">25</xref>.</p></sec></sec></body><back><ack><p>We thank Sukumari Mohan and Akos Szilvasi for excellent technical assistance, Apinya Ngam-ek for modifying the green fluorescent protein plasmid, and Paul Rennert for helpful advice.</p></ack><ref-list><ref id="R1"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Gravestein</surname><given-names>L.A.</given-names></name><name><surname>Borst</surname><given-names>J.</given-names></name></person-group><article-title>Tumor necrosis factor receptor family members in the immune system</article-title><source>Semin. Immunol.</source><volume>10</volume><year>1998</year><fpage>423</fpage><lpage>434</lpage><pub-id pub-id-type="pmid">9826575</pub-id></citation></ref><ref id="R2"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Schneider</surname><given-names>P.</given-names></name><name><surname>MacKay</surname><given-names>F.</given-names></name><name><surname>Steiner</surname><given-names>V.</given-names></name><name><surname>Hofmann</surname><given-names>K.</given-names></name><name><surname>Bodmer</surname><given-names>J.-L.</given-names></name><name><surname>Holler</surname><given-names>N.</given-names></name><name><surname>Ambrose</surname><given-names>C.</given-names></name><name><surname>Lawton</surname><given-names>P.</given-names></name><name><surname>Bixler</surname><given-names>S.</given-names></name><name><surname>Acha-Orbea</surname><given-names>H.</given-names></name></person-group><article-title>BAFF, a novel ligand of the tumor necrosis factor family, stimulates B cell growth</article-title><source>J. Exp. Med.</source><volume>189</volume><year>1999</year><fpage>1747</fpage><lpage>1756</lpage><pub-id pub-id-type="pmid">10359578</pub-id></citation></ref><ref id="R3"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Shu</surname><given-names>H.-B.</given-names></name><name><surname>Hu</surname><given-names>W.-H.</given-names></name><name><surname>Johnson</surname><given-names>H.</given-names></name></person-group><article-title>TALL-1 is a novel member of the TNF family that is down-regulated by mitogens</article-title><source>J. Leukoc. Biol.</source><volume>65</volume><year>1999</year><fpage>680</fpage><lpage>683</lpage><pub-id pub-id-type="pmid">10331498</pub-id></citation></ref><ref id="R4"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Mukhopadhyay</surname><given-names>A.</given-names></name><name><surname>Ni</surname><given-names>J.</given-names></name><name><surname>Zhai</surname><given-names>Y.</given-names></name><name><surname>Yu</surname><given-names>G.-L.</given-names></name><name><surname>Aggarwal</surname><given-names>B.B.</given-names></name></person-group><article-title>Identification and characterization of a novel cytokine, THANK, a TNF homologue that activates apoptosis, nuclear factor-κB, and c-Jun NH<sub>2</sub>-terminal kinase</article-title><source>J. Biol. Chem.</source><volume>274</volume><year>1999</year><fpage>15978</fpage><lpage>15981</lpage><pub-id pub-id-type="pmid">10347144</pub-id></citation></ref><ref id="R5"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Moore</surname><given-names>P.A.</given-names></name><name><surname>Belvedere</surname><given-names>O.</given-names></name><name><surname>Orr</surname><given-names>A.</given-names></name><name><surname>Pieri</surname><given-names>K.</given-names></name><name><surname>LaFleur</surname><given-names>D.W.</given-names></name><name><surname>Feng</surname><given-names>P.</given-names></name><name><surname>Soppet</surname><given-names>D.</given-names></name><name><surname>Charters</surname><given-names>M.</given-names></name><name><surname>Gentz</surname><given-names>R.</given-names></name><name><surname>Parmelee</surname><given-names>D.</given-names></name></person-group><article-title>BLySmember of the tumor necrosis factor family and B lymphocyte stimulator</article-title><source>Science.</source><volume>285</volume><year>1999</year><fpage>260</fpage><lpage>263</lpage><pub-id pub-id-type="pmid">10398604</pub-id></citation></ref><ref id="R6"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>MacKay</surname><given-names>F.</given-names></name><name><surname>Woodcock</surname><given-names>S.A.</given-names></name><name><surname>Lawton</surname><given-names>P.</given-names></name><name><surname>Ambrose</surname><given-names>C.</given-names></name><name><surname>Baetscher</surname><given-names>M.</given-names></name><name><surname>Schneider</surname><given-names>P.</given-names></name><name><surname>Tschopp</surname><given-names>J.</given-names></name><name><surname>Browning</surname><given-names>J.L.</given-names></name></person-group><article-title>Mice transgenic for BAFF develop lymphocytic disorders along with autoimmune manifestations</article-title><source>J. Exp. Med.</source><volume>190</volume><year>1999</year><fpage>1697</fpage><lpage>1710</lpage><pub-id pub-id-type="pmid">10587360</pub-id></citation></ref><ref id="R7"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Laabi</surname><given-names>Y.</given-names></name><name><surname>Gras</surname><given-names>M.-P.</given-names></name><name><surname>Carbonnel</surname><given-names>F.</given-names></name><name><surname>Brouet</surname><given-names>J.C.</given-names></name><name><surname>Berger</surname><given-names>R.</given-names></name><name><surname>Larsen</surname><given-names>C.J.</given-names></name><name><surname>Tsapis</surname><given-names>A.</given-names></name></person-group><article-title>A new gene, BCM, on chromosome 16 is fused to the interleukin 2 gene by a t(4;16)(q26;p13) translocation in a malignant T cell lymphoma</article-title><source>EMBO (Eur. Mol. Biol. Organ.) J.</source><volume>11</volume><year>1992</year><fpage>3897</fpage><lpage>3904</lpage></citation></ref><ref id="R8"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Laabi</surname><given-names>Y.</given-names></name><name><surname>Gras</surname><given-names>M.-P.</given-names></name><name><surname>Brouet</surname><given-names>J.-C.</given-names></name><name><surname>Berger</surname><given-names>R.</given-names></name><name><surname>Larsen</surname><given-names>C.-J.</given-names></name><name><surname>Tsapis</surname><given-names>A.</given-names></name></person-group><article-title>The BCMA gene, preferentially expressed during B lymphoid maturation, is bidirectionally transcribed</article-title><source>Nucleic Acids Res.</source><volume>22</volume><year>1994</year><fpage>1147</fpage><lpage>1154</lpage><pub-id pub-id-type="pmid">8165126</pub-id></citation></ref><ref id="R9"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Gras</surname><given-names>M.-P.</given-names></name><name><surname>Laabi</surname><given-names>Y.</given-names></name><name><surname>Linares-Cruz</surname><given-names>G.</given-names></name><name><surname>Blondel</surname><given-names>M.-O.</given-names></name><name><surname>Rigaut</surname><given-names>J.-P.</given-names></name><name><surname>Brouet</surname><given-names>J.-C.</given-names></name><name><surname>Leca</surname><given-names>G.</given-names></name><name><surname>Haguenauer-Tsapis</surname><given-names>R.</given-names></name><name><surname>Tsapis</surname><given-names>A.</given-names></name></person-group><article-title>BCMApan integral membrane protein in the Golgi apparatus of human mature B lymphocytes</article-title><source>Int. Immunol.</source><volume>7</volume><year>1995</year><fpage>1093</fpage><lpage>1106</lpage><pub-id pub-id-type="pmid">8527407</pub-id></citation></ref><ref id="R10"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Madry</surname><given-names>C.</given-names></name><name><surname>Laabi</surname><given-names>Y.</given-names></name><name><surname>Callebaut</surname><given-names>I.</given-names></name><name><surname>Roussel</surname><given-names>J.</given-names></name><name><surname>Hatzoglou</surname><given-names>A.</given-names></name><name><surname>Coniat</surname><given-names>M.L.</given-names></name><name><surname>Mornon</surname><given-names>J.-P.</given-names></name><name><surname>Berger</surname><given-names>R.</given-names></name><name><surname>Tsapis</surname><given-names>A.</given-names></name></person-group><article-title>The characterization of murine BCMA gene defines it as a new member of the tumor necrosis factor receptor superfamily</article-title><source>Int. Immunol.</source><volume>10</volume><year>1998</year><fpage>1693</fpage><lpage>1702</lpage><pub-id pub-id-type="pmid">9846698</pub-id></citation></ref><ref id="R11"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Miller</surname><given-names>G.T.</given-names></name><name><surname>Hochman</surname><given-names>P.S.</given-names></name><name><surname>Meier</surname><given-names>W.</given-names></name><name><surname>Tizard</surname><given-names>R.</given-names></name><name><surname>Bixler</surname><given-names>S.A.</given-names></name><name><surname>Rosa</surname><given-names>M.D.</given-names></name><name><surname>Wallner</surname><given-names>B.P.</given-names></name></person-group><article-title>Specific interaction of lymphocyte function–associated antigen-3 with CD2 can inhibit T cell responses</article-title><source>J. Exp. Med.</source><volume>178</volume><year>1993</year><fpage>211</fpage><lpage>222</lpage><pub-id pub-id-type="pmid">7686212</pub-id></citation></ref><ref id="R12"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Majeau</surname><given-names>G.R.</given-names></name><name><surname>Meier</surname><given-names>W.</given-names></name><name><surname>Jimmo</surname><given-names>B.</given-names></name><name><surname>Kioussis</surname><given-names>D.</given-names></name><name><surname>Hochman</surname><given-names>P.S.</given-names></name></person-group><article-title>Mechanism of lymphocyte function-associated molecule 3-Ig fusion proteins inhibition of T cell responses. Structure/function analysis in vitro and in human CD2 transgenic mice</article-title><source>J. Immunol.</source><volume>152</volume><year>1994</year><fpage>2753</fpage><lpage>2767</lpage><pub-id pub-id-type="pmid">7511625</pub-id></citation></ref><ref id="R13"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Rennert</surname><given-names>P.D.</given-names></name><name><surname>James</surname><given-names>D.</given-names></name><name><surname>MacKay</surname><given-names>F.</given-names></name><name><surname>Browning</surname><given-names>J.L.</given-names></name><name><surname>Hochman</surname><given-names>P.S.</given-names></name></person-group><article-title>Lymph node genesis is induced by signaling through the lymphotoxin β receptor</article-title><source>Immunity</source><volume>9</volume><year>1998</year><fpage>71</fpage><lpage>79</lpage><pub-id pub-id-type="pmid">9697837</pub-id></citation></ref><ref id="R14"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Crowe</surname><given-names>P.D.</given-names></name><name><surname>VanArsdale</surname><given-names>T.L.</given-names></name><name><surname>Walter</surname><given-names>B.N.</given-names></name><name><surname>Ware</surname><given-names>C.F.</given-names></name><name><surname>Hession</surname><given-names>C.</given-names></name><name><surname>Ehrenfels</surname><given-names>B.</given-names></name><name><surname>Browning</surname><given-names>J.L.</given-names></name><name><surname>Din</surname><given-names>W.S.</given-names></name><name><surname>Goodwin</surname><given-names>R.G.</given-names></name><name><surname>Smith</surname><given-names>C.A.</given-names></name></person-group><article-title>A lymphotoxin-β-specific receptor</article-title><source>Science</source><volume>264</volume><year>1994</year><fpage>707</fpage><lpage>710</lpage><pub-id pub-id-type="pmid">8171323</pub-id></citation></ref><ref id="R15"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Schneider</surname><given-names>P.</given-names></name><name><surname>Bodmer</surname><given-names>J.-L.</given-names></name><name><surname>Thome</surname><given-names>M.</given-names></name><name><surname>Hofmann</surname><given-names>K.</given-names></name><name><surname>Holler</surname><given-names>N.</given-names></name><name><surname>Tschopp</surname><given-names>J.</given-names></name></person-group><article-title>Characterization of two receptors for TRAIL</article-title><source>FEBS Lett.</source><volume>416</volume><year>1997</year><fpage>329</fpage><lpage>334</lpage><pub-id pub-id-type="pmid">9373179</pub-id></citation></ref><ref id="R16"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Lefevre</surname><given-names>E.A.</given-names></name><name><surname>Krzysiek</surname><given-names>R.</given-names></name><name><surname>Loret</surname><given-names>E.P.</given-names></name><name><surname>Galanaud</surname><given-names>P.</given-names></name><name><surname>Richard</surname><given-names>Y.</given-names></name></person-group><article-title>Cutting edgeHIV-1 Tat protein differentially modulates the B cell response of naive, memory, and germinal center B cells</article-title><source>J. Immunol.</source><volume>163</volume><year>1999</year><fpage>1119</fpage><lpage>1122</lpage><pub-id pub-id-type="pmid">10415004</pub-id></citation></ref><ref id="R17"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Naismith</surname><given-names>J.H.</given-names></name><name><surname>Sprang</surname><given-names>S.R.</given-names></name></person-group><article-title>Modularity in the TNF-receptor family</article-title><source>Trends Biochem. Sci.</source><volume>23</volume><year>1998</year><fpage>74</fpage><lpage>79</lpage><pub-id pub-id-type="pmid">9538693</pub-id></citation></ref><ref id="R18"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Banner</surname><given-names>D.W.</given-names></name><name><surname>D'Arcy</surname><given-names>A.</given-names></name><name><surname>Janes</surname><given-names>W.</given-names></name><name><surname>Gentz</surname><given-names>R.</given-names></name><name><surname>Schoenfeld</surname><given-names>H.-J.</given-names></name><name><surname>Broger</surname><given-names>C.</given-names></name><name><surname>Loetscher</surname><given-names>H.</given-names></name><name><surname>Lesslauer</surname><given-names>W.</given-names></name></person-group><article-title>Crystal structure of the soluble human 55 kd TNF receptor-human TNFβ compleximplications for TNF receptor activation</article-title><source>Cell</source><volume>73</volume><year>1993</year><fpage>431</fpage><lpage>445</lpage><pub-id pub-id-type="pmid">8387891</pub-id></citation></ref><ref id="R19"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Mongkolsapaya</surname><given-names>J.</given-names></name><name><surname>Grimes</surname><given-names>J.M.</given-names></name><name><surname>Chen</surname><given-names>N.</given-names></name><name><surname>Xu</surname><given-names>X.N.</given-names></name><name><surname>Stuart</surname><given-names>D.I.</given-names></name><name><surname>Jones</surname><given-names>E.Y.</given-names></name><name><surname>Screaton</surname><given-names>G.R.</given-names></name></person-group><article-title>Structure of the TRAIL-DR5 complex reveals mechanisms conferring specificity in apoptotic initiation</article-title><source>Nat. Struct. Biol.</source><volume>6</volume><year>1999</year><fpage>1048</fpage><lpage>1053</lpage><pub-id pub-id-type="pmid">10542098</pub-id></citation></ref><ref id="R20"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Hymowitz</surname><given-names>S.G.</given-names></name><name><surname>Christinger</surname><given-names>H.N.</given-names></name><name><surname>Fuh</surname><given-names>G.</given-names></name><name><surname>Ultsch</surname><given-names>M.</given-names></name><name><surname>O'Connell</surname><given-names>M.</given-names></name><name><surname>Kelley</surname><given-names>R.F.</given-names></name><name><surname>Ashkenazi</surname><given-names>A.</given-names></name><name><surname>de Vos</surname><given-names>A.M.</given-names></name></person-group><article-title>Triggering cell deaththe crystal structure of Apo2L/TRAIL in a complex with death receptor 5</article-title><source>Mol. Cell</source><volume>4</volume><year>1999</year><fpage>563</fpage><lpage>571</lpage><pub-id pub-id-type="pmid">10549288</pub-id></citation></ref><ref id="R21"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Bennett</surname><given-names>M.</given-names></name><name><surname>Macdonald</surname><given-names>K.</given-names></name><name><surname>Chan</surname><given-names>S.W.</given-names></name><name><surname>Luzio</surname><given-names>J.P.</given-names></name><name><surname>Simari</surname><given-names>R.</given-names></name><name><surname>Weissberg</surname><given-names>P.</given-names></name></person-group><article-title>Cell surface trafficking of Fasa rapid mechanism of p53-mediated apoptosis</article-title><source>Science.</source><volume>282</volume><year>1998</year><fpage>290</fpage><lpage>293</lpage><pub-id pub-id-type="pmid">9765154</pub-id></citation></ref><ref id="R22"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Pillai</surname><given-names>S.</given-names></name></person-group><article-title>The chosen few? Positive selection and the generation of naive B lymphocytes</article-title><source>Immunity.</source><volume>10</volume><year>1999</year><fpage>493</fpage><lpage>502</lpage><pub-id pub-id-type="pmid">10367895</pub-id></citation></ref><ref id="R23"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Agenes</surname><given-names>F.</given-names></name><name><surname>Rosado</surname><given-names>M.M.</given-names></name><name><surname>Freitas</surname><given-names>A.A.</given-names></name></person-group><article-title>Independent homeostatic regulation of B cell compartments</article-title><source>Eur. J. Immunol.</source><volume>27</volume><year>1997</year><fpage>1801</fpage><lpage>1807</lpage><pub-id pub-id-type="pmid">9247595</pub-id></citation></ref><ref id="R24"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Fulcher</surname><given-names>D.A.</given-names></name><name><surname>Basten</surname><given-names>A.</given-names></name></person-group><article-title>Influences on the lifespan of B cell subpopulations defined by different phenotypes</article-title><source>Eur. J. Immunol.</source><volume>27</volume><year>1997</year><fpage>1188</fpage><lpage>1199</lpage><pub-id pub-id-type="pmid">9174610</pub-id></citation></ref><ref id="R25"><citation citation-type="journal"><person-group person-group-type="author"><name><surname>Gross</surname><given-names>J.A.</given-names></name><name><surname>Johnston</surname><given-names>J.</given-names></name><name><surname>Mudri</surname><given-names>S.</given-names></name><name><surname>Enselman</surname><given-names>R.</given-names></name><name><surname>Dillon</surname><given-names>S.R.</given-names></name><name><surname>Madden</surname><given-names>K.</given-names></name><name><surname>Xu</surname><given-names>W.</given-names></name><name><surname>Parrish-Novak</surname><given-names>J.</given-names></name><name><surname>Foster</surname><given-names>D.</given-names></name><name><surname>Lofton-Day</surname><given-names>C.</given-names></name></person-group><article-title>TACI and BCMA are receptors for a TNF homologue implicated in B-cell autoimmune disease</article-title><source>Nature.</source><volume>404</volume><year>2000</year><fpage>995</fpage><lpage>999</lpage><pub-id pub-id-type="pmid">10801128</pub-id></citation></ref></ref-list><fn-group><fn><p>J.S. Thompson and P. Schneider contributed equally to this work.</p></fn><fn><p>Portions of this work have appeared in abstract form (2000. <italic>Scand. J. Immunol.</italic> 51:65).</p></fn></fn-group></back><floats-wrap><table-wrap position="float" id="T1"><label>Table 1</label><caption><p>The Total Number of Splenocytes and Splenic Subpopulations Examined after Treatment with BCMA-Ig</p></caption><table frame="hsides" rules="groups"><thead><tr valign="bottom"><th align="left">Mouse</th><th align="center">Total cells</th><th align="center">B cells</th><th align="center">CD4<sup>+</sup> T cells</th><th align="center">CD8<sup>+</sup> T cells</th><th align="center">Neutrophils</th><th align="center">Mac-1<sup>+</sup> cells</th></tr></thead><tbody><tr valign="bottom"><td align="left">BCMA-Ig treated</td><td align="center"></td><td align="center"></td><td align="center"></td><td align="center"></td><td align="center"></td><td align="center"></td></tr><tr valign="bottom"><td align="left">B1</td><td align="char" char=".">58.5</td><td align="char" char=".">21.5</td><td align="char" char=".">16.9</td><td align="char" char=".">7.5</td><td align="char" char=".">4.6</td><td align="char" char=".">12.1</td></tr><tr valign="bottom"><td align="left">B2</td><td align="char" char=".">66.0</td><td align="char" char=".">24.4</td><td align="char" char=".">19.5</td><td align="char" char=".">8.3</td><td align="char" char=".">3.9</td><td align="char" char=".">12.4</td></tr><tr valign="bottom"><td align="left">B3</td><td align="char" char=".">46.5</td><td align="char" char=".">11.7</td><td align="char" char=".">14.9</td><td align="char" char=".">8.3</td><td align="char" char=".">3.4</td><td align="char" char=".">10.0</td></tr><tr valign="bottom"><td align="left">B4</td><td align="char" char=".">36.0</td><td align="char" char=".">11.0</td><td align="char" char=".">12.7</td><td align="char" char=".">6.5</td><td align="char" char=".">2.2</td><td align="char" char=".">6.9</td></tr><tr valign="bottom"><td align="center">Mean ± SD</td><td align="char" char=".">51.8 ± 11.4</td><td align="char" char=".">17.2 ± 5.9</td><td align="char" char=".">16.0 ± 2.5</td><td align="char" char=".">7.7 ± 0.7</td><td align="char" char=".">3.5 ± 0.9</td><td align="char" char=".">10.4 ± 2.2</td></tr><tr valign="bottom" align="left"><td>Controls</td><td></td><td></td><td></td><td></td><td></td><td></td></tr><tr valign="bottom"><td align="left">A1</td><td align="char" char=".">73.5</td><td align="char" char=".">40.4</td><td align="char" char=".">17.9</td><td align="char" char=".">6.2</td><td align="char" char=".">4.1</td><td align="char" char=".">13.3</td></tr><tr valign="bottom"><td align="left">A2</td><td align="char" char=".">72.8</td><td align="char" char=".">39.1</td><td align="char" char=".">16.1</td><td align="char" char=".">6.6</td><td align="char" char=".">4.5</td><td align="char" char=".">13.7</td></tr><tr valign="bottom"><td align="left">A3</td><td align="char" char=".">81.8</td><td align="char" char=".">42.9</td><td align="char" char=".">20.4</td><td align="char" char=".">9.2</td><td align="char" char=".">3.8</td><td align="char" char=".">13.2</td></tr><tr valign="bottom"><td align="left">A4</td><td align="char" char=".">43.5</td><td align="char" char=".">21.6</td><td align="char" char=".">10.4</td><td align="char" char=".">4.2</td><td align="char" char=".">3.2</td><td align="char" char=".">9.0</td></tr><tr valign="bottom"><td align="center">Mean ± SD</td><td align="char" char=".">67.9 ± 14.5</td><td align="char" char=".">36.0 ± 8.4</td><td align="char" char=".">16.2 ± 3.7</td><td align="char" char=".">6.6 ± 1.8</td><td align="char" char=".">3.9 ± 0.5</td><td align="char" char=".">12.3 ± 1.9</td></tr><tr valign="bottom"><td align="left"><italic>P</italic> values</td><td align="center"><italic>P</italic> > 0.1</td><td align="center"><bold><italic>P</italic></bold>= <bold>0.02</bold></td><td align="center"><italic>P</italic> > 0.1</td><td align="center"><italic>P</italic> > 0.1</td><td align="center"><italic>P</italic> > 0.1</td><td align="center"><italic>P</italic> > 0.1</td></tr></tbody></table><table-wrap-foot><fn><p>The number of cells (×10<sup>6</sup>) from individual mice in each group is shown. <italic>P</italic> values were determined by Student's <italic>t</italic> test.</p></fn></table-wrap-foot></table-wrap><fig position="float" id="F1"><label>Figure 1</label><caption><p>The extracellular domain of BCMA interacts with BAFF. (A) Human BCMA-Ig and various control TNFR-Ig molecules were mixed with Flag-tagged TNF ligands, immunoprecipitated (IP) with protein A Sepharose, and analyzed by Western blot (WB). Receptor-Ig is revealed with anti–human IgG (top), and coimmunoprecipitating ligands are detected using anti-Flag M2 antibody (bottom). α, anti-. (B) Interaction of BAFF with BCMA assayed by surface plasmon resonance (BIAcore). (C) BCMA-Ig binds stable 293 cell line expressing surface full-length BAFF. The wild-type 293 cells or a stable cell line expressing BAFF (reference 2) were stained with media containing similar amounts of BCMA-Ig, TNFR2-Ig, TRAILR2-Ig, or control media using PE-conjugated anti-hIgG1 (left and middle). The presence of surface BAFF was detected using an anti-hBAFF rat mAb, 43.9 (reference 2; right). (D) BCMA-Ig blocks BAFF binding to Raji cells. Various concentrations of either BCMA-Ig or LTβR-Ig were preincubated with Flag-BAFF, then added to Raji cells. BAFF binding was detected with the anti-Flag M2 antibody and analyzed by flow cytometry.</p></caption><graphic xlink:href="JEM000648.f1"></graphic></fig><fig position="float" id="F2"><label>Figure 2</label><caption><p>Cell surface expression of BCMA in transfected and primary cells. (A) 293E cells were cotransfected with expression vectors for green fluorescent protein (GFP) and full-length human BCMA or a control plasmid. Surface expression of BCMA was detected with either an anti-BCMA antibody (top) or Flag-BAFF (bottom). (B) Human tonsillar B cells and the U266 plasmocytic cell line were stained with either anti-BCMA, control rabbit antibody, or Flag-BAFF, and were analyzed by flow cytometry.</p></caption><graphic xlink:href="JEM000648.f2"></graphic></fig><fig position="float" id="F3"><label>Figure 3</label><caption><p>Administration of BCMA-Ig reduces the peripheral B cell population. Adult Balb/c mice were treated with four intraperitoneal injections of BCMA-Ig or control Ig over a period of 11 d. At day 19, splenic B220<sup>+</sup> B cells, CD4<sup>+</sup> and CD8<sup>+</sup> T cells, and Gr1<sup>+</sup> and Mac-1<sup>+</sup> populations were analyzed by flow cytometry. A representative mouse from each group is shown.</p></caption><graphic xlink:href="JEM000648.f3"></graphic></fig><fig position="float" id="F4"><label>Figure 4</label><caption><p>BAFF promotes the survival of splenocytes in vitro. (A) Forward (FSC) and side scatter (SSC) profiles of murine splenocytes in culture after 72 h in the presence or absence of BAFF. The R2 gate contains live cells (annexin V and propidium iodide negative). (B) Percentage of R2 cells surviving. BAFF concentration was 2 μg/ml, and fusion proteins were added at 10 μg/ml. This is a representative experiment of the assay done ∼10 times.</p></caption><graphic xlink:href="JEM000648.f4"></graphic></fig></floats-wrap></pmc></record>Pour manipuler ce document sous Unix (Dilib)
EXPLOR_STEP=$WICRI_ROOT/Wicri/Asie/explor/AustralieFrV1/Data/Pmc/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 0011250 | SxmlIndent | more
Ou
HfdSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd -nk 0011250 | SxmlIndent | more
Pour mettre un lien sur cette page dans le réseau Wicri
{{Explor lien
|wiki= Wicri/Asie
|area= AustralieFrV1
|flux= Pmc
|étape= Corpus
|type= RBID
|clé=
|texte=
}}
| This area was generated with Dilib version V0.6.33. |  |