The mouse lymph node as an ectopic transplantation site for multiple tissues
Identifieur interne : 004714 ( Pmc/Corpus ); précédent : 004713; suivant : 004715The mouse lymph node as an ectopic transplantation site for multiple tissues
Auteurs : Junji Komori ; Lindsey Boone ; Aaron Deward ; Toshitaka Hoppo ; Eric LagasseSource :
- Nature biotechnology [ 1087-0156 ] ; 2012.
Abstract
Cell-based therapy has been viewed as a promising alternative to organ transplantation, but cell transplantation aimed at organ repair is not always possible. Here, we show that the mouse lymph node can support the engraftment and growth of healthy cells from multiple tissues. Direct injection of hepatocytes into a single mouse lymph node generated enough ectopic liver mass to rescue survival of mice with lethal metabolic disease. Furthermore, thymuses transplanted into a lymph node of athymic nude mice generate a functional immune system capable of rejecting allogeneic and xenogeneic grafts. Finally, pancreatic islets injected into the lymph node of diabetic mice restore normal glucose control. Collectively, these results suggest the practical approach of targeting lymph nodes to restore, maintain or improve tissue and organ functions.
Url:
DOI: 10.1038/nbt.2379
PubMed: 23000933
PubMed Central: 3469750
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PMC:3469750Le document en format XML
<record><TEI><teiHeader><fileDesc><titleStmt><title xml:lang="en">The mouse lymph node as an ectopic transplantation site for multiple tissues</title><author><name sortKey="Komori, Junji" sort="Komori, Junji" uniqKey="Komori J" first="Junji" last="Komori">Junji Komori</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Boone, Lindsey" sort="Boone, Lindsey" uniqKey="Boone L" first="Lindsey" last="Boone">Lindsey Boone</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Deward, Aaron" sort="Deward, Aaron" uniqKey="Deward A" first="Aaron" last="Deward">Aaron Deward</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Hoppo, Toshitaka" sort="Hoppo, Toshitaka" uniqKey="Hoppo T" first="Toshitaka" last="Hoppo">Toshitaka Hoppo</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Lagasse, Eric" sort="Lagasse, Eric" uniqKey="Lagasse E" first="Eric" last="Lagasse">Eric Lagasse</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author></titleStmt><publicationStmt><idno type="wicri:source">PMC</idno><idno type="pmid">23000933</idno><idno type="pmc">3469750</idno><idno type="url">http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3469750</idno><idno type="RBID">PMC:3469750</idno><idno type="doi">10.1038/nbt.2379</idno><date when="2012">2012</date><idno type="wicri:Area/Pmc/Corpus">004714</idno><idno type="wicri:explorRef" wicri:stream="Pmc" wicri:step="Corpus" wicri:corpus="PMC">004714</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">The mouse lymph node as an ectopic transplantation site for multiple tissues</title><author><name sortKey="Komori, Junji" sort="Komori, Junji" uniqKey="Komori J" first="Junji" last="Komori">Junji Komori</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Boone, Lindsey" sort="Boone, Lindsey" uniqKey="Boone L" first="Lindsey" last="Boone">Lindsey Boone</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Deward, Aaron" sort="Deward, Aaron" uniqKey="Deward A" first="Aaron" last="Deward">Aaron Deward</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Hoppo, Toshitaka" sort="Hoppo, Toshitaka" uniqKey="Hoppo T" first="Toshitaka" last="Hoppo">Toshitaka Hoppo</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author><author><name sortKey="Lagasse, Eric" sort="Lagasse, Eric" uniqKey="Lagasse E" first="Eric" last="Lagasse">Eric Lagasse</name><affiliation><nlm:aff id="A1">McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</nlm:aff></affiliation></author></analytic><series><title level="j">Nature biotechnology</title><idno type="ISSN">1087-0156</idno><idno type="eISSN">1546-1696</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p id="P1">Cell-based therapy has been viewed as a promising alternative to organ transplantation, but cell transplantation aimed at organ repair is not always possible. Here, we show that the mouse lymph node can support the engraftment and growth of healthy cells from multiple tissues. Direct injection of hepatocytes into a single mouse lymph node generated enough ectopic liver mass to rescue survival of mice with lethal metabolic disease. Furthermore, thymuses transplanted into a lymph node of athymic nude mice generate a functional immune system capable of rejecting allogeneic and xenogeneic grafts. Finally, pancreatic islets injected into the lymph node of diabetic mice restore normal glucose control. Collectively, these results suggest the practical approach of targeting lymph nodes to restore, maintain or improve tissue and organ functions.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Fisher, Ra" uniqKey="Fisher R">RA Fisher</name></author><author><name sortKey="Strom, Sc" uniqKey="Strom S">SC Strom</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Shapiro, Am" uniqKey="Shapiro A">AM Shapiro</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Schuppan, D" uniqKey="Schuppan D">D Schuppan</name></author><author><name sortKey="Afdhal, Nh" uniqKey="Afdhal N">NH Afdhal</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Markert, Ml" uniqKey="Markert M">ML Markert</name></author></analytic></biblStruct><biblStruct><analytic><author><name sortKey="Markert, Ml" uniqKey="Markert M">ML Markert</name></author><author><name 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<front><journal-meta><journal-id journal-id-type="nlm-journal-id">9604648</journal-id><journal-id journal-id-type="pubmed-jr-id">20305</journal-id><journal-id journal-id-type="nlm-ta">Nat Biotechnol</journal-id><journal-id journal-id-type="iso-abbrev">Nat. Biotechnol.</journal-id><journal-title-group><journal-title>Nature biotechnology</journal-title></journal-title-group><issn pub-type="ppub">1087-0156</issn><issn pub-type="epub">1546-1696</issn></journal-meta><article-meta><article-id pub-id-type="pmid">23000933</article-id><article-id pub-id-type="pmc">3469750</article-id><article-id pub-id-type="doi">10.1038/nbt.2379</article-id><article-id pub-id-type="manuscript">NIHMS404537</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>The mouse lymph node as an ectopic transplantation site for multiple tissues</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Komori</surname><given-names>Junji</given-names></name><xref ref-type="aff" rid="A1">1</xref><xref rid="FN2" ref-type="author-notes">*</xref></contrib><contrib contrib-type="author"><name><surname>Boone</surname><given-names>Lindsey</given-names></name><xref ref-type="aff" rid="A1">1</xref><xref rid="FN2" ref-type="author-notes">*</xref></contrib><contrib contrib-type="author"><name><surname>DeWard</surname><given-names>Aaron</given-names></name><xref ref-type="aff" rid="A1">1</xref><xref rid="FN2" ref-type="author-notes">*</xref></contrib><contrib contrib-type="author"><name><surname>Hoppo</surname><given-names>Toshitaka</given-names></name><xref ref-type="aff" rid="A1">1</xref><xref rid="FN3" ref-type="author-notes">2</xref></contrib><contrib contrib-type="author"><name><surname>Lagasse</surname><given-names>Eric</given-names></name><xref ref-type="aff" rid="A1">1</xref></contrib></contrib-group><aff id="A1"><label>1</label>McGowan Institute for Regenerative Medicine, Department of Pathology, University of Pittsburgh School of Medicine, Pittsburgh PA</aff><author-notes><corresp id="FN1">Correspondence: Eric Lagasse, PharmD, PhD., McGowan Institute for Regenerative Medicine, University of Pittsburgh, 450 Technology Drive. Room: 329, Pittsburgh, PA 15219, Phone: 412-624 5285, Fax: 412-624-5363, <email>Lagasse@pitt.edu</email></corresp><fn id="FN2" fn-type="equal"><label>*</label><p>These authors contributed equally to this work</p></fn><fn id="FN3" fn-type="present-address"><label>2</label><p>Current address, Department of Surgery, West Penn Allegheny Health System, Pittsburgh PA.</p></fn></author-notes><pub-date pub-type="nihms-submitted"><day>31</day><month>8</month><year>2012</year></pub-date><pub-date pub-type="epub"><day>23</day><month>9</month><year>2012</year></pub-date><pub-date pub-type="ppub"><month>10</month><year>2012</year></pub-date><pub-date pub-type="pmc-release"><day>10</day><month>4</month><year>2013</year></pub-date><volume>30</volume><issue>10</issue><fpage>976</fpage><lpage>983</lpage><pmc-comment>elocation-id from pubmed: 10.1038/nbt.2379</pmc-comment>
<permissions><license><license-p>Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:
<uri xlink:type="simple" xlink:href="http://www.nature.com/authors/editorial_policies/license.html#terms">http://www.nature.com/authors/editorial_policies/license.html#terms</uri></license-p></license></permissions><abstract><p id="P1">Cell-based therapy has been viewed as a promising alternative to organ transplantation, but cell transplantation aimed at organ repair is not always possible. Here, we show that the mouse lymph node can support the engraftment and growth of healthy cells from multiple tissues. Direct injection of hepatocytes into a single mouse lymph node generated enough ectopic liver mass to rescue survival of mice with lethal metabolic disease. Furthermore, thymuses transplanted into a lymph node of athymic nude mice generate a functional immune system capable of rejecting allogeneic and xenogeneic grafts. Finally, pancreatic islets injected into the lymph node of diabetic mice restore normal glucose control. Collectively, these results suggest the practical approach of targeting lymph nodes to restore, maintain or improve tissue and organ functions.</p></abstract></article-meta></front><body><sec sec-type="intro" id="S1"><title>Introduction</title><p id="P2">The shortage of organs available for transplant to terminally ill patients represents a major worldwide medical, social, and economic challenge. An alternative approach to whole-organ transplant involves the transplantation of cells to regenerate failing organs<sup><xref rid="R1" ref-type="bibr">1</xref>,<xref rid="R2" ref-type="bibr">2</xref></sup>. However orthotopic cell-based therapy directed at a diseased organ may not be feasible for many reasons, ranging from a possible lack of an appropriate environment in cirrhotic and fibrotic liver during end-stage disease to the lack of a thymus in complete DiGeorge Syndrome<sup><xref rid="R3" ref-type="bibr">3</xref>–<xref rid="R5" ref-type="bibr">5</xref></sup>. Consequently, a critical requirement of cell-based therapy for these patients is to establish an optimal <italic>in vivo</italic> site for cell and tissue transplantation to restore organ functions<sup><xref rid="R6" ref-type="bibr">6</xref>,<xref rid="R7" ref-type="bibr">7</xref></sup>.</p><p id="P3">The lymph node (LN) is a key organ of the mammalian immune system that has evolved to mount an immediate and orchestrated response against invading pathogens. The LN acts as a checkpoint where migrating T and B cells may encounter foreign antigen<sup><xref rid="R8" ref-type="bibr">8</xref>,<xref rid="R9" ref-type="bibr">9</xref></sup>. If a foreign antigen is identified, T cells undergo rapid cell division and also signal for help and recruit additional T cells<sup><xref rid="R8" ref-type="bibr">8</xref>,<xref rid="R9" ref-type="bibr">9</xref></sup>. To accommodate this sudden increase in cell number, lymphocytes need a special environment, which the LN provides.</p><p id="P4">Interestingly, the LN is also one of the first clinically observed sites of most cancer metastasis. Selected cancer cells will often migrate away from a primary tumor and colonize the LN<sup><xref rid="R10" ref-type="bibr">10</xref></sup>. Lymphatic vessels are designed to facilitate the uptake of surrounding fluid and cells, followed by transport of this fluid and cells to a nearby LN<sup><xref rid="R10" ref-type="bibr">10</xref></sup>. Therefore, malignant tumor cells take advantage of this route normally traveled by immune cells. Upon arrival in the LN, tumor cells can survive, perhaps because the architecture of the LN provides direct access to essential nutrients and growth factors found in the blood through the high endothelial venules. The LN also contains fibroblastic reticular cells and other stromal cells that secrete chemokines to enhance cell recruitment and survival<sup><xref rid="R8" ref-type="bibr">8</xref>,<xref rid="R9" ref-type="bibr">9</xref>,<xref rid="R11" ref-type="bibr">11</xref></sup>.</p><p id="P5">Because LNs support normal immune function as well as survival of metastatic tumor cells, LNs might also promote survival and expansion of healthy cells and tissues. Healthy cell and tissue growth in LNs would provide a new approach for cell therapies in regenerative medicine.</p><p id="P6">Here, we test the hypothesis that when transplanted directly into the LN of mice, three distinct healthy cell types would engraft and demonstrate ectopic organ functions <italic>in vivo</italic>. Previously, our lab showed that primary hepatocytes injected intraperitoneally into mice lacking fumarylacetoacetate hydrolase, (a mouse model of tyrosinemia type I) migrate and colonize the host abdominal lymphatics and restore hepatic functions<sup><xref rid="R13" ref-type="bibr">13</xref></sup>. Here, we show that hepatocytes injected directly into a single jejunal, popliteal, axillary, or periportal LN generate an ectopic hepatic mass and rescue mice from lethal liver failure. Furthermore, thymic tissue injected into a single jejunal LN of athymic nude mice generates a functional ectopic thymus. Finally, pancreatic islets transplanted in a single jejunal LN of streptozotocin induced diabetic mice engraft and secrete insulin to normalize glucose levels. These three independent results support the proof-of-concept that the LN provides a hospitable environment for normal cell engraftment and reveal a new approach to consider for future ectopic tissue and organ regeneration.</p></sec><sec sec-type="results" id="S2"><title>Results</title><sec id="S3"><title>Direct injection of hepatocytes into the LN</title><p id="P7">We targeted a single jejunal LN in the abdominal cavity of C57BL/6 wild type mice, which was selected because it is easily accessible and relatively large<sup><xref rid="R14" ref-type="bibr">14</xref></sup>. Upon injection of 0.1–0.5 million syngeneic primary hepatocytes, the LN enlarged slightly and no visible leakage was found, as evidenced by Evans blue dye (<xref rid="F1" ref-type="fig">Fig. 1a</xref>). One day after injection, syngeneic luciferase-expressing hepatocytes remained in the LN, as determined by <italic>in vivo</italic> imaging of luciferase (<xref rid="F1" ref-type="fig">Fig. 1b</xref>). In contrast, splenic and intraperitoneal injection of hepatocytes resulted in rapid dispersion of cells to the liver and throughout the abdominal cavity, respectively (<xref rid="F1" ref-type="fig">Fig. 1b</xref>). One week after transplant, syngeneic GFP+ hepatocytes were distributed mainly in the subcapsular sinus of the LN, but were not found in the LN follicle or germinal center (<xref rid="F1" ref-type="fig">Fig. 1c</xref>). Additionally, hepatocytes rapidly formed patches of hepatic tissue expressing E-cadherin (<xref rid="F1" ref-type="fig">Fig. 1d</xref>). This hepatocyte-to-hepatocyte attachment may help to retain hepatocytes within the site of transplantation<sup><xref rid="R15" ref-type="bibr">15</xref></sup>. Furthermore, the cell trafficking molecule sphingosine-1-phosphate receptor 1 (S1PR1), which is necessary for the egress of B and T cells from LNs <sup><xref rid="R16" ref-type="bibr">16</xref>,<xref rid="R17" ref-type="bibr">17</xref></sup>, was not present on hepatocytes in the LN. On the other hand, CCR7, a molecule known to control the migration of memory T cells and/or tumor cells into LNs <sup><xref rid="R18" ref-type="bibr">18</xref></sup>, was expressed by hepatocytes in the LN (<xref rid="F1" ref-type="fig">Fig. 1d</xref>). These observations suggest a potential mechanism of retention of healthy hepatocytes in the LN.</p><p id="P8">To assess whether the engrafted hepatocytes in the LN proliferate in response to growth stimuli in C57BL/6 wild type recipient mice, we performed partial hepatectomy (PHx) one week after syngeneic hepatocyte injection into the LN and added bromodeoxyuridine (BrdU) to the drinking water of recipient mice. PHx is a physiologically relevant method of stimulating hepatocyte growth<sup><xref rid="R19" ref-type="bibr">19</xref></sup>. BrdU incorporation was analyzed in the LN engrafted hepatocytes 2 weeks after LN injection and compared with animals that were not subjected to PHx. The number of GFP-expressing hepatocytes and percent of BrdU<sup>+</sup> hepatocytes in the LN of the PHx group was significantly higher than in mice without PHx (<xref rid="F1" ref-type="fig">Fig. 1e</xref>), indicating that hepatocytes in the LN respond to growth stimuli after PHx.</p></sec><sec id="S4"><title>A functional ectopic liver in the LN</title><p id="P9">Next, we asked whether transplantation of syngeneic hepatocytes into a single jejunal LN of Fah<sup>−/−</sup> tyrosinemic mouse<sup><xref rid="R20" ref-type="bibr">20</xref>–<xref rid="R22" ref-type="bibr">22</xref></sup>, a model of lethal metabolic liver failure, would induce hepatocyte proliferation. Twelve weeks after hepatocyte injection into the LN, animals were rescued from lethal liver failure due to the newly hepatized growth in the jejunal LN (<xref rid="F2" ref-type="fig">Fig. 2</xref>). Hepatocyte engraftment was localized to the transplanted LN and was not observed in other LNs or in the native liver (<xref rid="F2" ref-type="fig">Fig. 2a</xref>), suggesting that lymphatic distribution of hepatocytes did not occur. The ‘hepatized’ LN was mostly composed of newly formed liver tissue containing Fah<sup>+</sup>GFP<sup>+</sup> hepatocytes, but also included remnants of the lymphatic system as revealed by surrounding LYVE1<sup>+</sup> lymphatic endothelial cells (<xref rid="F2" ref-type="fig">Fig. 2b</xref>). The LN was transformed into a hepatic organoid composed of characteristically cuboidal hepatocytes, but with the absence of a biliary system<sup><xref rid="R13" ref-type="bibr">13</xref></sup>. To define the hepatized LN microarchitecture, we stained recipient LN for ER-TR7, a marker of fibroblastic reticular cells (FRCs), dipeptidyl peptidase-4 (DPP IV), a marker for brush borders of hepatocytes and bile canaliculi organization, and glutamine synthetase (GS), a marker of zonality for hepatocytes surrounding the terminal hepatic venules<sup><xref rid="R23" ref-type="bibr">23</xref></sup> (<xref rid="F2" ref-type="fig">Fig. 2b</xref>). GFP<sup>+</sup> hepatocytes resided in cellular proximity with ER-TR7<sup>+</sup> FRCs. FRCs are known to play a crucial role in establishing the reticular network as well as regulating immune function<sup><xref rid="R11" ref-type="bibr">11</xref>,<xref rid="R24" ref-type="bibr">24</xref></sup>. Similar to what is observed in normal liver anatomy, DPP IV was localized throughout the hepatized LN. Moreover, GS<sup>+</sup> hepatocytes were identified surrounding some of the hepatic veins in the newly formed liver tissue. Notably, we observed survival of the animals (<xref rid="F2" ref-type="fig">Fig. 2c</xref>) and long-term persistence (over 25 weeks) of the graft after transplantation to the LN (<xref rid="F2" ref-type="fig">Fig. 2a</xref>) and no immune-responsiveness as indicated by the presence of very few lymphocytes and macrophages around the transplantation zone (<xref rid="SD1" ref-type="supplementary-material">Supplementary Fig. 1</xref>).</p><p id="P10">We then tested if this transplantation method is effective in other LNs throughout the body, since all LNs share a common histological architecture<sup><xref rid="R9" ref-type="bibr">9</xref>,<xref rid="R14" ref-type="bibr">14</xref>,<xref rid="R25" ref-type="bibr">25</xref></sup>. We injected syngeneic hepatocytes into single extra-abdominal axillary or popliteal LNs in Fah<sup>−/−</sup>mice (<xref rid="F2" ref-type="fig">Fig. 2a</xref>). Similar to the intra-abdominal jejunal LN injection, we observed a single, large, hepatized LN several weeks after cell transplantation, which subsequently rescued mice from lethal liver failure (<xref rid="F2" ref-type="fig">Fig. 2c</xref>). In wild type mice, a jejunal LN weighs around 25±3 mg whereas a popliteal or axillary LN weighs 3±1 mg (n=5). Because the jejunal LN is the largest LN in the mouse, it was consequently easier to inject and lead to a higher survival rate (<xref rid="F2" ref-type="fig">Fig. 2c</xref>). Furthermore, when we compared the mass of hepatic tissue generated in the intra-abdominal jejunal LN to the extra-abdominal axillary and popliteal LNs, we found no statistical differences, indicating no tissue growth advantage between these 3 LNs (<xref rid="F2" ref-type="fig">Fig. 2d</xref>). Transplantation of hepatocytes into a periportal LN, one of the closest LNs to the liver, also resulted in a large hepatized LN and rescued the mice from lethal liver disease. However, transplantation of a LN closer to the location of the liver did not appear to be beneficial for the experimental outcome when compared with the other transplanted LNs (<xref rid="F2" ref-type="fig">Fig. 2d</xref>).</p><p id="P11">Thus far all transplantations used syngeneic donor and recipient mice. Because LNs perform a central function for allogeneic recognition<sup><xref rid="R26" ref-type="bibr">26</xref></sup>, we next tested whether successful engraftment is possible in allogeneic LN. We injected C57BL/6-GFP<sup>+</sup> hepatocytes into the liver (via splenic injection) or into the LN of 129sv FAH<sup>−/−</sup> recipient mice. 129sv and C57BL/6 mice share the major histocompatibility complex haplotype H2<sup>b</sup> but differ in minor histocompatibility antigens and are considered allogeneic<sup><xref rid="R27" ref-type="bibr">27</xref>,<xref rid="R28" ref-type="bibr">28</xref></sup>. While C57BL/6 hepatocytes transplanted into 129sv FAH<sup>−/−</sup> recipients failed to engraft (<xref rid="F2" ref-type="fig">Fig. 2e</xref>), blocking the co-stimulation pathways CD28/B7 (blocked by CTLA4Ig) and CD40/CD40L (blocked by MR1)<sup><xref rid="R29" ref-type="bibr">29</xref>,<xref rid="R30" ref-type="bibr">30</xref></sup> in the 129sv FAH<sup>−/−</sup> recipients facilitated successful engraftment of C57BL/6-GFP<sup>+</sup> hepatocytes injected into either the spleen or the LN (<xref rid="F2" ref-type="fig">Fig. 2e</xref>). This result shows that the immune reaction to transplanted cells in LNs is not stronger or faster compared to cells transplanted in another site.</p></sec><sec id="S5"><title>A functional ectopic thymus in the LN</title><p id="P12">Using a similar approach, we asked if <italic>de novo</italic> thymus function could be generated in LNs of athymic mice. Thymuses were harvested from newborn C57BL/6 GFP<sup>+</sup> transgenic mice, minced and injected directly into the jejunal LN or under the kidney capsule of athymic BALB/c Nude mice. After one month, recipient mouse blood was analyzed by flow cytometry for the presence of recipient (GFP ) single positive (SP) CD4<sup>+</sup> and CD8<sup>+</sup> T cells. Thymic transplant into the LN (LN Tx Nude) or under the kidney capsule (KC Tx Nude) generated circulating recipient SP CD4<sup>+</sup> and CD8<sup>+</sup> T cells (<xref rid="F3" ref-type="fig">Fig. 3a</xref>, <xref rid="SD1" ref-type="supplementary-material">Supplementary Fig. 2</xref>). Ten months after transplantation, SP CD4<sup>+</sup> and CD8<sup>+</sup> T cells were still present in the peripheral blood indicating long-term thymic engraftment in the LN (<xref rid="SD1" ref-type="supplementary-material">Supplementary Fig. 3</xref>). Interestingly, transplantation of a thymic single cell suspension also resulted in the presence of SP CD4<sup>+</sup> and CD8<sup>+</sup> T cells, although to a lesser degree than transplantation of minced thymic tissues (<xref rid="SD1" ref-type="supplementary-material">Supplementary Table 1</xref>). Newborn GFP<sup>+</sup> mice were used as a source of donor thymuses because they contain minimal mature thymocytes. In fact, less than 6% (n=3/54) of recipient mice showed any donor GFP<sup>+</sup> T cell contamination in the blood one month after transplant, when measured by flow cytometry (data not shown). These three mice were excluded from further studies.</p><p id="P13">We then harvested the ectopic thymuses for further characterization of the engraftment. GFP<sup>+</sup> epithelial thymic cells remained within the injected LN and were organized into an epithelial thymic structure (<xref rid="F3" ref-type="fig">Fig. 3b</xref>). Previously, thymic epithelia have been distinguished by their cytokeratin 5 (K5) and cytokeratin 8 (K8) phenotypes<sup><xref rid="R31" ref-type="bibr">31</xref></sup>. The ectopic thymuses were present in the subcapsular sinus of the LN (<xref rid="SD1" ref-type="supplementary-material">Supplementary Fig. 4</xref>) and contained both K5 and K8 positive regions, which correspond with thymic medullary and cortical epithelia, respectively (<xref rid="F3" ref-type="fig">Fig. 3b</xref>). Ectopic thymuses were also analyzed for the presence of recipient double positive (DP) CD4<sup>+</sup>CD8<sup>+</sup> thymocytes, which represent immature T cells undergoing thymic selection<sup><xref rid="R32" ref-type="bibr">32</xref></sup>. The ectopic thymuses contained recipient DP thymocytes as well as SP CD4<sup>+</sup> and CD8<sup>+</sup> T cells, indicating a selective mechanism of T cell commitment and maturation (<xref rid="F3" ref-type="fig">Fig. 3b</xref>).</p><p id="P14">To more fully characterize the T cell phenotypes generated in the LN Tx Nude mice, we analyzed the T cell receptor (TCR) repertoire by flow cytometry staining with antibodies recognizing different TCR Vβ segments (Vβ 2, 3, 4, 5.1–5.2, 6, 7, 8.1–8.2, 8.3, 9, 10<sup>b</sup>, 11, 12, 13, 14, and 17<sup>a</sup>). Each Vβ was detected on CD3<sup>+</sup> T cells of C57BL/6 wild type splenocytes. Heterozygous BALB/c Nude mouse splenocytes expressed 10 out of 15 Vβ segments, consistent with known partial or complete genetic deletions of certain Vβ segments (Vβ 3, 5.1–5.2, 9, 11 and 12) in this strain. Importantly, splenocytes in LN Tx Nude recipients expressed a Vβ profile similar to the heterozygous BALB/c Nude mice (<xref rid="F3" ref-type="fig">Fig. 3c</xref>). These results demonstrate that a C57BL/6 ectopic thymus promotes development of T cells generated from the bone marrow of recipient BALB/c Nude mice.</p><p id="P15">We then further characterized the splenic T cells in LN Tx Nude mice by flow cytometry to determine whether regulatory, naïve, central memory, and effector memory T cell subsets are present. Regulatory T cells were detected by analyzing FoxP3 expression in CD4<sup>+</sup>CD25<sup>+</sup> T cells. We observed similar percentages of regulatory T cells in splenocytes from C57BL/6, heterozygous Nude, and LN Tx Nude mice (<xref rid="F3" ref-type="fig">Fig. 3d</xref>). Naïve and memory T cells were distinguished by the differential expression of CD44 and CD62L (naïve: CD44<sup>−</sup>CD62L<sup>+</sup>, central memory: CD44<sup>+</sup>CD62L<sup>+</sup>, and effector memory: CD44<sup>+</sup>CD62L<sup>−</sup>). As with the regulatory T cells, we detected naïve and memory T cell subsets among splenocytes from C57BL/6, heterozygous Nude, and LN Tx Nude mice (<xref rid="F3" ref-type="fig">Fig. 3d</xref>). The percentage of effector memory T cells was higher and naïve T cells was lower in the LN Tx Nude mice, perhaps because these mice had been previously exposed to skin grafts (see below).</p><p id="P16">Since LN Tx Nude mice contained a range of peripheral SP CD4 and CD8 T cells, we asked if the <italic>de novo</italic> immune system in these recipient mice could mount a T cell-mediated response against a skin allograft. Tail skin from C57BL/6 (syngeneic with regard to the donor thymus) or CBA/CaJ (allogeneic with regard to the donor thymus) mice was transplanted to the dorsal side of LN Tx BALB/c Nude mice. After 2 weeks, all of the LN Tx BALB/c Nude mice had rejected the allogeneic CBA/CaJ skin grafts. On the other hand, the C57BL/6 skin grafts were completely accepted after 2 weeks (<xref rid="F3" ref-type="fig">Fig. 3e</xref>). We then asked if LN Tx BALB/c Nude mice would also mount an immune response against a xenogeneic tumor cell transplant. 300,000 human colorectal cancer cells<sup><xref rid="R33" ref-type="bibr">33</xref></sup> were injected into the subcutaneous space of BALB/c Nude and LN Tx BALB/c Nude mice. The majority (8 of 9) of injected LN Tx BALB/c Nude mice rejected the tumors (<xref rid="F3" ref-type="fig">Fig. 3e</xref>). In contrast, xenogeneic tumors grew in untreated BALB/c Nude mice (<xref rid="F3" ref-type="fig">Fig. 3e</xref>). These results suggest that the SP T cells present in LN Tx BALB/c Nude mice were functional. Together, these data support the concept of using the LN as a site for thymic transplant to generate an ectopic thymus.</p></sec><sec id="S6"><title>Functional pancreatic islets in the LN</title><p id="P17">Finally, we hypothesized that the LN would also provide a suitable environment for pancreatic islet transplantation. Islets were harvested from C57BL/6 GFP<sup>+</sup> transgenic mice and transplanted into the jejunal LN of C57BL/6 wild type mice treated with streptozotocin, which induces diabetes. Blood glucose levels were monitored weekly and the transplanted LN was eventually removed to analyze islet engraftment.</p><p id="P18">GFP<sup>+</sup> islets were found within the subcapsular sinus of the LN, adjacent to the densely packed lymphocytes indicative of a typical LN (<xref rid="F4" ref-type="fig">Fig. 4a</xref>). We detected expression of C-peptide and glucagon, markers of pancreatic β-cell and α-cell function, respectively, within the engrafted LN (<xref rid="F4" ref-type="fig">Fig. 4a</xref>).</p><p id="P19">Next, we asked whether islets transplanted to the LN of diabetic mice (blood glucose levels greater than 300 mg/dL) are able to lower blood glucose levels to a normal range (blood glucose levels between 100–200 mg/dL). Similar to islets transplanted under the kidney capsule, islets transplanted directly into the LN restored mean blood glucose levels to normal levels within six weeks after transplantation (<xref rid="F4" ref-type="fig">Fig. 4b</xref>). In 3 of 5 LN Tx mice, a second islet transplant was performed into the jejunal LN one week after the initial transplant. Furthermore, normoglycemia was maintained in the one mouse examined at six months for at least six months after LN transplantation (data not shown). These results suggest that pancreatic islets transplanted in the LN survive and function <italic>in vivo</italic> with the capacity to sustain long-term normoglycemia.</p><p id="P20">Because we observed engraftment of multiple cell types in the LN, we asked whether activation of a LN-mediated immune response might interfere with the function of the engrafted cells. Therefore, we induced an inflammatory reaction in the intraperitoneal cavity of normoglycemic mice that had received islet transplants into their LN; to induce the inflammatory reaction we injected mice with lipopolysaccharide (LPS, 1 mg/kg). We confirmed the effective induction of inflammation by measuring the serum levels of tumor necrosis factor α (TNF α), interleukin 1β (IL-1β), and IL-6 (<xref rid="F4" ref-type="fig">Fig. 4c</xref>). Immediately after LPS injection, we noted a temporary reduction in mouse weight and blood glucose levels, which completely normalized after four days (<xref rid="F4" ref-type="fig">Fig. 4c</xref>). We did not observe any increase in glucose levels above normal levels (normoglycemia was still detected 5 weeks after LPS injection). Together, these data suggest no apparent negative effect of the lymphatic or immune systems on LN-grafted islets.</p></sec><sec id="S7"><title>Vasculature of injected LN</title><p id="P21">We demonstrated that cell engraftment in the LN is not restricted to one cell type. This result is consistent with the current concept of metastasis to the LN, where multiple cancer cell types are capable of residing, and suggests that the LN environment is exceptionally well suited to promote survival and function of transplanted cells in general. Because abundant vasculature is required to sustain organ function<sup><xref rid="R6" ref-type="bibr">6</xref>,<xref rid="R34" ref-type="bibr">34</xref></sup>, we hypothesize that the dense vascular network in the LN is an important contributor to sustain long-term engraftment of normal epithelial tissue. We observed dense neovascular trees in the LNs into which hepatocytes had been injected (<xref rid="F5" ref-type="fig">Fig. 5a</xref>). LN injected with hepatocytes, thymic cells or islets contained many recipient derived CD31<sup>+</sup> endothelial cells pervading the areas of engraftment, suggesting that extensive blood vessel remodeling took place during ectopic tissue engraftment (<xref rid="F5" ref-type="fig">Fig. 5b</xref><bold>and</bold><xref rid="SD1" ref-type="supplementary-material">Supplementary Fig. 5</xref>). Moreover, we detected CD105<sup>+</sup> (Endoglin) cells and Collagen IV<sup>+</sup> cells, which are markers of neovascular remodeling, in each of the engrafted LNs (<xref rid="F5" ref-type="fig">Fig. 5b</xref>)<sup><xref rid="R35" ref-type="bibr">35</xref>–<xref rid="R37" ref-type="bibr">37</xref></sup>. These data suggest that blood vessels in the surrounding LN environment contribute to the neovascularization and overall function of the ectopic tissues.</p></sec></sec><sec sec-type="discussion" id="S8"><title>Discussion</title><p id="P22">There are over 500 LNs in the human body, many of which are relatively easily accessible. While a single LN structurally limits the number of donor cells that can be transplanted, it is technically feasible to transplant more than one LN in order to gain sufficient organ/tissue function from the transplanted cells. The potential loss of function in a few LNs does not appear to compromise the overall function of the lymphatic system. In fact, lymphedema is the most common complication following lymphadenectomy in patients with cancer and only affects a limited number of patients<sup><xref rid="R38" ref-type="bibr">38</xref></sup>. Compression syndrome and lymphatic spread are two of the common issues found in cancer patients with metastatic diseases in their LNs. However, none of these complications were observed in any of our experiments. It is also important to note that we transplanted healthy, not transformed, cells into LNs, so the intrinsic potential of transformed cells for widespread metastatic migration and uncontrolled growth is not present in our experiments. Large animal studies will provide further insight into potential difficulties associated with cell transplant to the LN.</p><p id="P23">LN biopsies by fine-needle aspiration are a routine diagnostic procedure with LNs often being readily identified by palpation or using ultrasound guidance. In fact, the clinical application of LN injection has been validated, with patients rating the procedure as less painful than venous puncture<sup><xref rid="R39" ref-type="bibr">39</xref></sup>. Moreover, if a less superficial node is advantageous for therapy, ultrasound guidance can be used to successfully inject the visceral mesenteric LNs<sup><xref rid="R40" ref-type="bibr">40</xref></sup>. The strong clinical precedent of ultrasound-guided LN injections may help make this technique readily adaptable to a clinical setting. These minimally invasive techniques may also allow a potential therapy for patients who are ineligible for a more invasive therapy due to co-morbidities.</p><p id="P24">In the treatment of liver failure, transplantation of hepatocytes into ectopic sites, including the spleen, pancreas, peritoneal cavity, and subrenal capsule has been proposed. Feasibility and efficacy of these techniques have been confirmed in preclinical studies, but clinical success rates have been limited thus far and new methods are needed to improve hepatocyte engraftment<sup><xref rid="R1" ref-type="bibr">1</xref>,<xref rid="R7" ref-type="bibr">7</xref></sup>. It should be noted that our goal is not to replace a whole liver but to complement liver functions by generating functional ectopic hepatic tissue. In the Fah<sup>−/−</sup> mice, we generated around 70% of the liver mass in one LN. The native liver is still present, however at a reduced size and probably at reduced function. For patients with liver disease, we postulate that liver function gradually deteriorates and that transplantation of several LNs with hepatocytes will create enough hepatic mass to stabilize the liver disease. In addition, we hypothesize that hepatic mass generated in the LN may provide enough hepatic function to facilitate regeneration of the native liver. It should also be noted that transplantation of heterotopic liver has been discussed at length in the literature as a possible option to orthotopic liver transplantation <sup><xref rid="R35" ref-type="bibr">35</xref>,<xref rid="R41" ref-type="bibr">41</xref>,<xref rid="R42" ref-type="bibr">42</xref></sup>.</p><p id="P25">Thymus transplants have been performed exclusively in the quadriceps of pediatric patients with complete DiGeorge Syndrome<sup><xref rid="R4" ref-type="bibr">4</xref></sup>. Unfortunately, children with DiGeorge syndrome often show poor growth, and transplantation is frequently postponed to allow for further development<sup><xref rid="R43" ref-type="bibr">43</xref></sup>. Furthermore, a lack of vascularization and resulting ischemia following transplant is detrimental<sup><xref rid="R44" ref-type="bibr">44</xref></sup>. Transplanting thymic cells into the LN may represent an advantageous site to provide thymic function.</p><p id="P26">The optimal implantation site for pancreatic islet transplantation to increase function, reduce necessary implantation mass and decrease immunogenicity is still under debate <sup><xref rid="R6" ref-type="bibr">6</xref>,<xref rid="R12" ref-type="bibr">12</xref>,<xref rid="R45" ref-type="bibr">45</xref>,<xref rid="R46" ref-type="bibr">46</xref></sup>. But clearly, the proximity to a good vascular supply is essential for survival of islet cells, as well as for hepatocytes and thymic epithelial cells.</p><p id="P27">One concern for cell transplant into the LN is the rapid immune response that could be initiated by the introduction of foreign antigen into a site densely packed with lymphocytes. In our study, we included experiments under allogeneic conditions and blocked the T cell response to prevent any alloreactivity. We observed that the immune reaction in LNs is not stronger or faster than in other sites and that immune suppression therapy works at similar efficiency compared to the classic hepatocyte transplantation in the spleen. We expect that immunosuppressive therapies similar to those used in clinical organ transplants can be utilized with this approach.</p><p id="P28">Reprogramming of somatic cells provides an exciting potential source of donor cells for regenerative medicine<sup><xref rid="R47" ref-type="bibr">47</xref></sup>. Since these cells can be derived from autologous material and are capable of being recognized as “self” by the host immune system, they can potentially overcome immunologic barriers. However, recent studies suggest that these autologous cells may not be entirely protected from the immune system<sup><xref rid="R48" ref-type="bibr">48</xref></sup>. Based on our results, the LN may provide an effective transplantation site for reprogrammed somatic cells developed for organ regeneration purposes.</p><p id="P29">In summary, we provide the first report describing the use of a LN as a site for functional cellular transplant. By directly injecting the LN with hepatocytes, thymuses, or pancreatic islets, we demonstrate engraftment of the donor cells and subsequent organ function. This new approach of using the LN as an <italic>in vivo</italic> bioreactor in which to regenerate functional organs may be beneficial to the field of regenerative medicine.</p></sec><sec sec-type="methods" id="S9"><title>Methods</title><sec id="S10"><title>Animals and tissues</title><p id="P30">Donor 129sv mice and recipient 129sv Fah<sup>−/−</sup> mice were a kind gift from Dr. Markus Grompe (OHSU). For allogeneic experiments, donor hepatocytes were isolated from C57BL/6 GFP<sup>+</sup> mice (GFP transgene under the control of the human ubiquitin C promoter, C57BL/6-Tg(UBC-GFP)30Scha/J, Jackson Laboratory) and transplanted into 129sv Fah<sup>−/−</sup> mice. For syngeneic experiments using C57BL/6 GFP<sup>+</sup> hepatocytes, 129sv Fah<sup>−/−</sup> mice were backcrossed for more than eight generations with C57BL/6 mice (Jackson Laboratory) to generate C57BL/6 Fah<sup>−/−</sup> mice. Luciferase C57BL/6 transgenic mouse (Luc+), expressing firefly luciferase under the control of the broadly expressed beta-actin promoter were kindly provided by Dr. Thorn (University of Pittsburgh). Donor primary hepatocytes were isolated from adult (5–8 weeks old) mice. Donors and recipients were not matched according to gender. Newborn (1–3 day old) C57BL/6 GFP<sup>+</sup> mice were used as donors of thymic cells. Athymic BALB/c Nude-<italic>Foxn1<sup>nu</sup></italic> (Harlan) mice were used as recipients of thymic cells. Blood collection (100 microliters) was performed using the submandibular bleeding technique. Adult (5–8 weeks old) C57BL/6 GFP<sup>+</sup> mice were used as the donor of pancreatic islets. Adult (5–8 weeks old) C57BL/6 mice were used as recipients of pancreatic islets. Animals were bred and housed in the Division of Laboratory Animal Resources facility at the University of Pittsburgh Center for Biotechnology and Bioengineering. Experimental protocols followed National Institutes of Health guidelines for animal care and were approved by the Institutional Animal Care and Use Committee at the University of Pittsburgh.</p></sec><sec id="S11"><title>Hepatocyte Transplantation</title><p id="P31">Primary hepatocytes were isolated using the 2-step collagenase perfusion technique. The number and viability of cells were determined by trypan blue exclusion. 0.1–0.5 million viable cells were suspended in 20 μl Matrigel (BD Biosciences) for one recipient and kept on ice until transplantation. Recipient animals were anesthetized with 1–3% Isoflurane and laparotomized. The jejunal LN was exposed and cells were injected using a 28 G needle under a dissecting scope (Leica). Just after injection, the contact site was clipped for 5 minutes by micro clamp to prevent cell leakage. In Fah<sup>−/−</sup> mice experiments, the mice were kept on 2-(2-nitro-4-trifluoromethylbenzoyl)-1,3-cyclohexanedione (NTBC)-containing drinking water at a concentration of 8mg/L until transplantation. NTBC was discontinued just after surgery. For extra-abdominal LN injections, we injected 3% Evans blue solution intradermally into the footpad of the hind or forelimb before cell transplant to visualize the small popliteal or axillary LN.</p></sec><sec id="S12"><title>Thymic Transplantation</title><p id="P32">Thymuses were harvested from newborn GFP transgenic mice and cut into small fragments. The jejunal LNs were exposed and cells were injected with minced thymus tissue through a 20 G needle. Thymus tissue was also grafted beneath the kidney capsule as a positive control. For the kidney capsule experiments, an incision was made on the left side of the peritoneal cavity and the kidney exposed. A small hole was made in the capsule and the thymus was inserted between the kidney capsule and parenchyma. Light cauterization was used to seal the opening. The wound was closed with surgical sutures.</p></sec><sec id="S13"><title>Pancreatic Islet Transplantation</title><p id="P33">Recipient C57BL/6 mice were injected with 190 mg/kg streptozotocin (Sigma) intraperitoneally to induce diabetes. Diabetes (blood glucose greater than 300 mg/dL) was confirmed three days after injection using a Contour Blood Glucose Meter (Bayer). The pancreases from adult C57BL/6 GFP<sup>+</sup> transgenic mice were perfused with Collagenase P (Roche) through the bile duct. Digested islets were washed in HBSS/FBS and placed in a 70 μm cell strainer. The larger size cell strainer content was transferred to a petri dish and individual islets were picked and counted under a dissecting microscope. Approximately 200–300 islets were mixed with 10 ul of matrigel and loaded into a 27 G insulin syringe on ice. For LN transplantation, a small incision was made in the abdomen to expose the jejunal LN. The syringe containing islets was inserted into the LN and islets were slowly injected. For kidney capsule transplantation, a small incision over the left kidney was performed to expose the kidney. A hole was made in the capsule and islets were delivered similar to the LN. Light cauterization was used to seal the opening. The wound was then closed with surgical sutures. If a decrease in glucose level was not observed after one week, a second islet transplant was performed in the same LN.</p></sec><sec id="S14"><title>In vivo Imaging</title><p id="P34">To detect donor luciferase<sup>+</sup> C57BL/6 hepatocytes, we used an IVIS200 system (Caliper LifeScience) following intraperitoneal injection of 200 μl of 30 mg/mL luciferin substrate into recipient C57BL/6 mice and anesthesia with 3% isoflurane. Images were analyzed using LivingImage software (Caliper LifeScience).</p></sec><sec id="S15"><title>Proliferation Assay</title><p id="P35">Primary hepatocytes from C57BL/6 GFP<sup>+</sup> mice were transplanted into 11 mice as described above. Recipient mice were given drinking water containing 0.8 mg/mL BrdU immediately following surgery. After one week, we sacrificed 3 mice for analysis. Partial hepatectomy (PHx), in which two-thirds of the liver of a mouse is removed, was then performed on 5 of the 11 mice and the remaining 3 mice were used for controls. One week later, all 8 mice were sacrificed for analysis. Using histological sections, we determined the amount of hepatocyte engraftment in the LN by counting GFP<sup>+</sup> hepatocytes and determined the ratio of proliferating hepatocytes by counting BrdU<sup>+</sup> hepatocytes.</p></sec><sec id="S16"><title>Allogeneic transplantation</title><p id="P36">Primary hepatocytes from C57BL/6 GFP<sup>+</sup> mice were transplanted into ten 129sv Fah<sup>−/−</sup> mice by LN or splenic injection. Five out of ten mice from each group were intraperitoneally injected with the immunosuppressive drugs CTLA1Ig (0.25mg) and MR1 (0.25mg), a kind gift from Dr. Fadi Lakkis (University of Pittsburgh), on day 0, 2, 4 and 6 after transplantation.</p></sec><sec id="S17"><title>Antibodies</title><p id="P37">Antibodies specific for the following antigens were purchased for immunohistochemistry: ER-TR7, LYVE1, GFP, Glutamine Synthetase, CCR7, S1PR1 (EDG1), F4/80 (Abcam), PNAd, B220, CD4 CD8 and Gr-1 (BD Biosciences), BrdU (Santa Cruz biotechnology), DPPIV (AbD Serotec), E-Cadherin (Zymed), Keratin 5 (Covance), Keratin 8 (DSHB), and C-peptide and Glucagon (Cell Signaling Technologies). Antibodies specific for the following antigens were purchased for flow cytometric analysis: APC mouse-CD3ε, APC-Cy7 mouse-CD8α, PE-Cy7-mouse CD45, PE mouse-CD4, mouse Vβ TCR screening panel, mouse naïve/memory T cell panel (Pharmingen), and mouse Treg detection kit (Miltenyi). Appropriate isotype control antibodies (BD Biosciences) were used to estimate background fluorescence.</p></sec><sec id="S18"><title>Immunohistochemistry</title><p id="P38">Tissue was fixed in 4% paraformaldehyde for 4 hours, stored in 30% sucrose for 12 hours and then embedded in OCT medium, frozen, and stored at −80° C. Sections (5–10μm) were mounted on glass slides and fixed in cold acetone for 10 minutes. For IHC staining, sections were washed with PBS and blocked with 5% BSA or milk for 30 minutes. Sections were then incubated with primary antibody for 1 hour and secondary antibody for 30 minutes. Sections were mounted with Hoechst mounting media. Images were captured with an Olympus FluoView 1000 Confocal Microscope or an Olympus IX71 inverted microscope.</p></sec><sec id="S19"><title>Flow Cytometry</title><p id="P39">Whole blood was collected in K<sub>2</sub>EDTA collection tubes (Terumo Medical). One hundred microliters of blood was added to cold FACS tubes. Antibodies were added at a dilution of 1/10 in blood and mixed by gentle pipetting. Reactions were incubated in the dark in an ice-slurry bath for 30 minutes. Three mL of Red Blood Cell Lysing Buffer (Sigma) was added to each tube, lightly vortexed and incubated for an additional 5 minutes. Two mL of flow buffer (2% FBS in HBSS) was added to the tubes, mixed, and centrifuged at 500g for 5 minutes. The supernatant was aspirated and secondary antibody was added at a dilution of 1/50 in flow buffer and mixed by gentle pipetting. Reactions were incubated in the dark in an ice-slurry bath for 15 minutes. Red blood cell lysis and centrifuge were repeated as described. Final cell pellet was resuspended in 400 μl of flow buffer with propidium iodide. Cells were analyzed using the BD FACSVantage Cell Sorter, a BD Aria II Cell Sorter, or a Miltenyi MACSQuant.</p></sec><sec id="S20"><title>Tail Skin Graft</title><p id="P40">Recipient mice (BALB/c Nude) containing an ectopic thymus (C57BL/6) in the LN were anesthetized and the tail skin (5×5mm) from CBA/CaJ or C57BL/6 mice was grafted on the left and right lateral sides of the superior dorsal region of the recipient mouse, respectively. A bandage was applied and removed 7 days following surgery. The grafts were observed daily for rejection.</p></sec><sec id="S21"><title>Tumor Cell Transplantation</title><p id="P41">Human metastatic colon cancer cells (Tu#12) were prepared and transplanted into mice as previously described<sup><xref rid="R33" ref-type="bibr">33</xref></sup>. Briefly, 3×10<sup>5</sup> cells were transplanted by subcutaneous injections. Tumor size was recorded after 2 months.</p></sec><sec id="S22"><title>LPS induced inflammation</title><p id="P42">LPS (1 mg/kg, Sigma) was injected intraperitoneally into C57BL/6 wild type or normoglycemic mice that previously received an islet transplant to the LN. Mice were bled to determine glucose levels or to measure serum cytokine levels. Cytokine level was determined by ELISA assay for TNF, IL-1β, and IL-6 (eBioscience).</p></sec><sec id="S23"><title>Statistical Analysis</title><p id="P43">Statistical significance was determined with an unpaired two-tailed Student’s t-test for data in <xref rid="F1" ref-type="fig">Fig 1e</xref>, <xref rid="F2" ref-type="fig">2d</xref>, <xref rid="F3" ref-type="fig">3a</xref>.</p></sec></sec><sec sec-type="supplementary-material" id="S24"><title>Supplementary Material</title><supplementary-material content-type="local-data" id="SD1"><label>1</label><caption><p id="P44"><bold>Supplementary Figure 1</bold>. Distribution of immune cells in the hepatized jejunal LN of a rescued C57BL/6 Fah<sup>−/−</sup> mice at 12 weeks after transplantation. Left to right panels, immunostaining of frozen LN serial sections with mAbs (red) against CD4/CD8 (CD4 and CD8 T cells), Gr-1 (granulocytes) and F4/80 (macrophages) with the presence of C57BL/6 GFP<sup>+</sup> hepatocytes (green). All sections were counterstained with Hoechst 33342 (blue). Scale bar: 100μm.</p><p id="P45"><bold>Supplementary Figure 2</bold>. Representative flow cytometry analysis of peripheral blood T cells. Analysis of CD4 and CD8 T cells from C57BL/6 GFP<sup>+</sup> mice, wild type C57BL/6, BALB/c Nude, kidney capsule (KC) transplanted (Tx) BALB/c Nude, and lymph node (LN) transplanted BALB/c Nude mice. The number values assigned to the gates and quadrants represent the percentage of total live cells within that gate or quadrant. All contour plots display 10% probability contours.</p><p id="P46"><bold>Supplementary Figure 3</bold>. Presence of peripheral T cells 10 months after C57BL/6 GFP<sup>+</sup> thymic transplantation in BALB/c Nude LN. (<bold>a</bold>) Blood analysis of 3 mice; the number values assigned represent the percentage of total live CD4 and CD8 T cells. (<bold>b</bold>) Flow cytometric analysis of mouse L084. The number values assigned to the gates and quadrants represent the percentage of total live cells within that gate or quadrant. All contour plots display 10% probability contours.</p><p id="P47"><bold>Supplementary Figure 4</bold>. C57BL/6 GFP<sup>+</sup> thymic tissue engrafts in the subcapsular space of the jejunal BALB/c Nude LN. Frozen section of an ectopic thymus with GFP<sup>+</sup> donor thymic cells and stained with cytokeratin 8 (K8) in red. Hoechst counterstain is shown in blue. Scale bar: 100μm.</p><p id="P48"><bold>Supplementary Figure 5</bold>. Engrafted C57BL/6 GFP<sup>+</sup> islet vasculature is derived from the recipient C57BL/6 mouse 6 weeks after transplantation. Immunostaining against CD31 (red) does not co-stain with the GFP<sup>+</sup> donor derived islets (green). Scale bar: 50μm.</p><p id="P49"><bold>Supplementary Table 1</bold>. Presence of peripheral T cells after transplant of C57BL/6 GFP<sup>+</sup> thymic cell suspension in the jejunal lymph node of a BALB/c Nude mouse. Flow cytometric analysis of peripheral blood T cells and gating strategy was used as described previously. Samples L039-L043 received LN transplants of 6×10<sup>6</sup> thymic cells prepared from a digestion of neonate thymus with 0.25% Collagenase Type IV. Samples L044-L046 received LN transplants of 1×10<sup>5</sup> thymic cells that were enriched for EpCAM using a MACS cell separation column (Miltenyi Biotech).</p></caption><media xlink:href="NIHMS404537-supplement-1.pdf" mimetype="application" mime-subtype="pdf" orientation="portrait" xlink:type="simple" id="d37e964" position="anchor"></media></supplementary-material></sec></body><back><ack id="S25"><p>We would like to thank S. Thorne and R. Sikorski for the <italic>in vivo</italic> imaging. This project used UPCI shared resources that are supported in part by award P30CA047904. This work was supported by the NIH grant R01 DK085711 (J.K., L.B., A.D., and E.L.).</p></ack><fn-group><fn id="FN4" fn-type="con"><p><bold>Contributions</bold></p><p>J.K., L.B., and A.D. performed and analyzed experiments for liver, thymus and pancreatic islets respectively. T.H. conducted experiments. J.K., L.B., AD and E.L. designed experiments and wrote manuscript; E.L., overall project planning and coordination. 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(<bold>a</bold>) Jejunal LN (yellow dotted oval) not transplanted (top panel) and just after transplantation (bottom panel) with hepatocytes. Primary hepatocytes were mixed with 3% Evans blue dye and Matrigel before injection. (<bold>b</bold>) <italic>In vivo</italic> optical imaging of animals transplanted at different sites. Primary hepatocytes from luciferase transgenic mice were transplanted in a single jejunal or popliteal LN, in spleen (SP) or intraperitoneally (IP). Signals (blue to red) depict different concentrations of donor hepatocytes at day 1 (top panels) and 1 week (bottom panels) after transplant. (<bold>c</bold>) Distribution of donor hepatocytes in a single jejunal LN. Top left panel, whole mount imaging of a LN one week after injection of donor GFP<sup>+</sup> hepatocytes. Bright field was merged with fluorescence. Top middle to bottom right panels, immunofluorescent (IF) staining of frozen LN serial sections with mAbs (red) against ER-TR7 (reticular fibroblasts), LYVE-1 (lymphatic vessels), PNAd (high endothelial venules), B220 (B cells) and CD4/CD8 (CD4 T and CD8 T cells) with the presence of GFP<sup>+</sup> hepatocytes (green). (<bold>d</bold>) IF staining of donor GFP+ hepatocytes (green) in jejunal LN one week after transplantation. Serial sections were stained with mAbs (red) against E-Cadherin (ECad), C-C chemokine receptor type 7 (CCR7) and sphingosine-1-phosphate receptor 1 (S1PR1). Nativel iver sections were stained as control (right panels). In native liver, CCR7 (red) was co-stained with dipeptidyl peptidase-4 (DPPIV) (green). All sections were counterstained with Hoechst 33342 (blue). (<bold>e</bold>) Proliferation of engrafted hepatocytes in LN after partial hepatectomy (PHx). Paraffin sections of injected LN and corresponding native liver one and two weeks after transplantation. Sections were stained for GFP (one and two weeks after transplantation) and BrdU (two weeks after transplantation), and revealed by peroxidase (brown cytoplasmic and brown nuclei staining respectively). Sections were counterstained with hematoxylin. Yellow outlines mark small populations of GFP<sup>+</sup> hepatocytes. 2 weeks after transplantation, bar graphs show the number of GFP<sup>+</sup> hepatocytes and % of BrdU<sup>+</sup> hepatocytes observed per section after immunostaining from animals with or without PHx.* P<0.05, ** P<0.0001. Data (mean + sem) are representative of one experiment with three to five mice per group. The experiment was repeated two times. Scale bar: (a) 1mm, (c–e) 100μm.</p></caption><graphic xlink:href="nihms404537f1"></graphic></fig><fig id="F2" orientation="portrait" position="float"><label>Figure 2</label><caption><p>Direct injection of hepatocytes into a single LN of a Fah<sup>−/−</sup> mouse. (<bold>a</bold>) Macroscopic appearances of non-transplanted and transplanted (hepatized) LN; LN are marked by yellow dotted oval). For non-transplanted axillary and popliteal LN, Evans blue was injected to highlight the presence of the LN.. The representative images of the jejunal, axillary and popliteal hepatized LN were captured at 12, 22, 25 weeks after transplantation respectively. (<bold>b</bold>) Histology of hepatized jejunal LN in rescued Fah<sup>−/−</sup>mice. Left panels, serial sections of hepatized LN composed of hepatic and lymphatic tissue. Sections are stained with hematoxylin and eosin (H&E)(top left panel), Fah (brown) and counterstained with hematoxylin (blue)(middle left panel). The immunofluorescence shows lymphatic vessels (LYVE1, red) and hepatocytes (GFP<sup>+</sup>, green)(bottom left panel). Right panels, higher magnification of H&E showing typical cuboidal hepatocytes. Reticular fibroblasts stain with antibodies specific for ER-TR7 (red) while hepatocytes are GFP<sup>+</sup>, and stain with antibodies specific for DPPIV (red). Glutamine synthetase (GS, red) expression shows unique zonal restriction surrounding terminal hepatic venules. Sections were counterstained with Hoechst 33342 (blue). (<bold>c</bold>) Kaplan-Meier survival curves (top) and body weight (bottom) of Fah<sup>−/−</sup> mice transplanted in intra- and extra- (blue) abdominal LN vs no treatment. Error bars show standard error. (<bold>d</bold>) Comparison of transplant efficiency in different sites. Left panels, macroscopic appearances of normal and hepatized LN (yellow dotted ovals) in the periportal area. Right top panel, Kaplan-Meier survival curves of Fah<sup>−/−</sup> mice transplanted into the jejunal vs periportal LN. Right lower panels, average weight of periportal vs jejunal LN and intra- vs extra- abdominal LN. No statistical difference was observed. Error bars show s.e.m. (<bold>e</bold>) Top panels, allogeneic transplantation in LN (LN Tx) and splenic injection (SP Tx). GFP<sup>+</sup> hepatocytes (C57BL/6 background) were transplanted into Fah<sup>−/−</sup> mice (129 sv background) by SP Tx and LN Tx and after NTBC removal (lack of NTBC in drinking water induces liver failure in Fah<sup>−/−</sup> mice). Where indicated, mice were injected with immunosuppressive agents CTLA4-Ig and MR1 on day 0, 2, 4 and 6 after transplantation. The experiment was repeated at least 2 times. Lower panels show one representative LN Tx mouse injected with CTLA4-Ig and MR1. Macroscopic appearance of hepatized jejunal LN (yellow dotted oval). Immunostaining of the hepatized LN for the presence of GFP+ (green) and Fah+ (red) hepatocytes as well as reticular fibroblasts (ER-TR7, red). Sections were counterstained with Hoechst 33342 (blue). Scale bar: (a, d and e, left panels) 5mm, (b, left panels) 1mm and (b, middle right and e middle right panels) 100μm.</p></caption><graphic xlink:href="nihms404537f2"></graphic></fig><fig id="F3" orientation="portrait" position="float"><label>Figure 3</label><caption><p>Functional ectopic thymus in the jejunal LN. (<bold>a</bold>) Flow cytometric analysis of peripheral blood T cells. Top panels, representative analysis of the gating strategy for CD4 and CD8 T cells in wild type C57BL/6 (WT), BALB/c Nude (Nude), and BALB/c Nude mice into which C57BL/6 GFP<sup>+</sup> thymic cells were injected into a jejunal LN (LN Tx Nude) mice. The number values assigned to the gates and quadrants represent the percentage of total live cells within that gate or quadrant. All contour plots display 10% probability contours. Lower panels show the percentage of CD3<sup>+</sup>, CD3<sup>+</sup>CD4<sup>+</sup> and CD3<sup>+</sup>CD8<sup>+</sup> live T cells in the blood of each animal analyzed (each symbol represents one animal); animals were WT, Nude, KC Tx Nude (BALB/c Nude Transplanted under Kidney Capsule) and LN Tx Nude. The thin black line indicates the mean +/− sem. No statistical significance (n.s.) was observed between KC and LN transplantation in each of the 3 panels. (<bold>b</bold>) Left panels, representative flow cytometric analysis of cells present in wild type C57BL/6 (WT) thymus and LN, and LN of BALB/c Nude mice into which thymic cells were injected into the LN (LN Tx Nude). The number values assigned to the gates and quadrants represent the percentage of total live cells within that gate or quadrant. Right panels show (top left) whole mount jejunal LN of a Nude mouse engrafted in LN with GFP<sup>+</sup> thymic cells. Bright field was merged with fluorescence, Top right shows frozen section with GFP<sup>+</sup> donor thymic cells. Bottom right shows immunostaining of cytokeratin 5 (K5) (blue), cytokeratin 8 (K8) (red) and counterstaining with Hoechst (white). Bottom left shows WT native thymus stained for K5 (red) and K8 (green). Scale bar: 200μm. (<bold>c</bold>) Flow cytometric analysis of TCR Vβ segment expression in splenocytes from wild type C57BL/6 mice (WT C57BL/6), heterozygous BALB/c Nude mice (Het Nude), or LN transplanted BALB/c Nude mice (LN Tx). Bar graphs show the mean percentage of the particular Vβ receptor. Individual symbols represent data from a single mouse (n=4–5). (<bold>d</bold>) Flow cytometric analysis of regulatory, naïve, central memory, and effector memory T cell subsets in splenocytes. Dot plots and histograms show gating strategy to detect regulatory T cells (FoxP3<sup>+</sup> fraction of CD4<sup>+</sup>CD25<sup>+</sup> T cells) and naïve (CD44<sup>−</sup>CD62L<sup>+</sup>), central memory (CD44<sup>+</sup>CD62L<sup>+</sup>), and effector memory (CD44<sup>+</sup>CD62L<sup>−</sup>) T cells. Graphs show the data from individual mice, labeled as in panel <bold>c</bold>. The thin black line indicates the mean. (<bold>e</bold>) Top panel, Kaplan-Meier curves showing survival of skin grafts from C57BL/6 or CBA/CaJ donor mice transplanted onto BALB/c Nude recipients that had previously undergone transplantation of C57BL/6 thymic cells into the LN. Middle panel, graph of tumor growth in athymic BALB/c Nude (nu/nu) mice. 300,000 human colon cancer cells<sup><xref rid="R33" ref-type="bibr">33</xref></sup> were inoculated subcutaneously with matrigel. Tumor sizes were measured once per week using a caliper and calculated as (π/6) × (length (mm) × width<sup>2</sup> (mm<sup>2</sup>)). The experiment was terminated after 8 weeks. Values are mean +/− s.e.m., n=10. Bottom panel, presence (+) or absence (−) of tumor growth after a single subcutaneous injection of 300,000 human colorectal cancer cells into BALB/c Nude recipients that had previously undergone transplantation of C57BL/6 thymic cells into the LN (LN Tx Nude), BALB/c Nude (Nude) recipients or C57BL/6 wild-type (WT) recipients.</p></caption><graphic xlink:href="nihms404537f3"></graphic></fig><fig id="F4" orientation="portrait" position="float"><label>Figure 4</label><caption><p>Ectopic pancreas generation in the jejunal LN after islet transplantation. (<bold>a</bold>) Top panel shows whole mount LN of a streptozotocin-treated diabetic C57BL/6 mouse engrafted with C57BL/6 GFP<sup>+</sup> pancreatic islets. Bright field was merged with fluorescence. Other panels show immunofluorescence (IF) of LN removed 6 weeks after engraftment. Staining with antibodies specific for ERTR7 (reticular fibroblasts), C-peptide (C-PEP), and glucagon (GLUC) is shown in red and GFP is shown in green and Hoechst counterstain is shown in blue. (<bold>b</bold>) Average blood glucose levels in diabetic recipient mice over the course of 10 weeks after transplantation of islets into the jejunal LN (LN Tx, n=5), under the kidney capsule (KC Tx, n=3), and without transplantation (No Tx, n=6). In 3 of 5 LN Tx mice, a second islet transplant was performed into the jejunal LN one week after the initial transplant. The mice that did not receive a transplant all died after 3 weeks. The data are presented as mean +/− s.e.m. (<bold>c</bold>) Average body weight (top) and blood glucose level (middle) of C57BL/6 wild-type (WT) mice or C57BL/6 LN Tx mice after LPS injection (1 mg/kg). Bottom panel shows average serum concentrations of tumor necrosis factor alpha (TNFα), IL1-β, and IL-6 two hours after LPS injection. All error bars show standard error. All IF image scale bars are 100 μm unless otherwise indicated.</p></caption><graphic xlink:href="nihms404537f4"></graphic></fig><fig id="F5" orientation="portrait" position="float"><label>Figure 5</label><caption><p>Neo-vascularization of ectopic tissue. (<bold>a</bold>) Vascular trees are shown in a native LN and native liver of a GFP transgenic mouse, and in mice after hepatocyte transplantation into the LN. (<bold>b</bold>) Immunostaining of LN injected with hepatocytes, thymic cells and pancreatic islets. Images were captured 12, 15, and 6 weeks after transplant of each tissue, respectively. CD31 is a marker for blood vessels and CD105 and Collagen IV are markers for neo-vascularization. Vasculature markers are shown in red and ectopic tissue is shown in green. All sections were counterstained with Hoechst 33342 in blue. All scale bars are 100μm.</p></caption><graphic xlink:href="nihms404537f5"></graphic></fig></floats-group></pmc></record>Pour manipuler ce document sous Unix (Dilib)
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|type= RBID
|clé= PMC:3469750
|texte= The mouse lymph node as an ectopic transplantation site for multiple tissues
}}
Pour générer des pages wiki
HfdIndexSelect -h $EXPLOR_AREA/Data/Pmc/Corpus/RBID.i -Sk "pubmed:23000933" \
| HfdSelect -Kh $EXPLOR_AREA/Data/Pmc/Corpus/biblio.hfd \
| NlmPubMed2Wicri -a LymphedemaV1
| This area was generated with Dilib version V0.6.31. |  |