Endothelial cell plasticity: how to become and remain a lymphatic endothelial cell
Identifieur interne : 003868 ( Ncbi/Merge ); précédent : 003867; suivant : 003869Endothelial cell plasticity: how to become and remain a lymphatic endothelial cell
Auteurs : Guillermo Oliver ; R. Sathish SrinivasanSource :
- Development (Cambridge, England) [ 0950-1991 ] ; 2010.
Abstract
Lineage commitment and differentiation into mature cell types are mostly considered to be unidirectional and irreversible processes. However, recent results have challenged this by showing that terminally differentiated cell types can be reprogrammed into other cell types, an important step towards devising strategies for gene therapy and tissue regeneration. In this Review, we summarize recent data on the earliest steps in the development of the mammalian lymphatic vasculature: the specification of lymphatic endothelial cells (LECs). We elaborate on a developmental model that integrates the different steps leading to LEC differentiation and lymphatic network formation, discuss evidence that suggests that LEC fate is plastic, and consider the potentially far-reaching implications of the ability to convert one cell type into another.
Url:
DOI: 10.1242/dev.035360
PubMed: 20081185
PubMed Central: 2858906
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<front><journal-meta><journal-id journal-id-type="nlm-ta">Development</journal-id><journal-id journal-id-type="publisher-id">develop</journal-id><journal-title-group><journal-title>Development (Cambridge, England)</journal-title></journal-title-group><issn pub-type="ppub">0950-1991</issn><issn pub-type="epub">1477-9129</issn><publisher><publisher-name>Company of Biologists</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="pmid">20081185</article-id><article-id pub-id-type="pmc">2858906</article-id><article-id pub-id-type="publisher-id">develop_137_3_007</article-id><article-id pub-id-type="doi">10.1242/dev.035360</article-id><article-categories><subj-group subj-group-type="heading"><subject>Reviews</subject></subj-group></article-categories><title-group><article-title>Endothelial cell plasticity: how to become and remain a lymphatic endothelial cell</article-title></title-group><contrib-group><contrib contrib-type="author"><name><surname>Oliver</surname><given-names>Guillermo</given-names></name><xref ref-type="corresp" rid="cor1">*</xref></contrib><contrib contrib-type="author"><name><surname>Srinivasan</surname><given-names>R. Sathish</given-names></name></contrib></contrib-group><aff id="d31e35">Department of Genetics and Tumor Cell Biology, St Jude Children's Research Hospital, 262 Danny Thomas Place, Memphis, TN 38105-3678, USA</aff><author-notes><corresp id="cor1"><label>*</label>Author for correspondence (<email>guillermo.oliver@stjude.org</email>)</corresp></author-notes><pub-date pub-type="ppub"><day>1</day><month>2</month><year>2010</year></pub-date><pub-date pub-type="pmc-release"><day>1</day><month>2</month><year>2011</year></pub-date><pmc-comment> PMC Release delay is 12 months and 0 days and was based on the copyright element. </pmc-comment>
<volume>137</volume><issue>3</issue><fpage>363</fpage><lpage>372</lpage><permissions><copyright-statement>© 2010.</copyright-statement><copyright-year>2010</copyright-year></permissions><self-uri xlink:title="pdf" xlink:href="363.pdf"></self-uri><abstract><title>Summary</title><p>Lineage commitment and differentiation into mature cell types are mostly considered to be unidirectional and irreversible processes. However, recent results have challenged this by showing that terminally differentiated cell types can be reprogrammed into other cell types, an important step towards devising strategies for gene therapy and tissue regeneration. In this Review, we summarize recent data on the earliest steps in the development of the mammalian lymphatic vasculature: the specification of lymphatic endothelial cells (LECs). We elaborate on a developmental model that integrates the different steps leading to LEC differentiation and lymphatic network formation, discuss evidence that suggests that LEC fate is plastic, and consider the potentially far-reaching implications of the ability to convert one cell type into another.</p></abstract><kwd-group><kwd>Prox1</kwd><kwd>Cell differentiation</kwd><kwd>Cell plasticity</kwd><kwd>Endothelial cell</kwd><kwd>Lymphatics</kwd></kwd-group></article-meta></front></pmc><affiliations><list></list><tree><noCountry><name sortKey="Oliver, Guillermo" sort="Oliver, Guillermo" uniqKey="Oliver G" first="Guillermo" last="Oliver">Guillermo Oliver</name><name sortKey="Srinivasan, R Sathish" sort="Srinivasan, R Sathish" uniqKey="Srinivasan R" first="R. Sathish" last="Srinivasan">R. Sathish Srinivasan</name></noCountry></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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