Show simple item record

dc.contributor.authorMelichar, Heather J.
dc.contributor.authorNarayan, Kavitha
dc.contributor.authorDer, Sandy D.
dc.contributor.authorHiraoka, Yoshiki
dc.contributor.authorGardiol, Noemie
dc.contributor.authorJeannet, Gregoire
dc.contributor.authorHeld, Werner
dc.contributor.authorChambers, Cynthia A.
dc.contributor.authorKang, Joonsoo
dc.date2022-08-11T08:09:01.000
dc.date.accessioned2022-08-23T16:15:51Z
dc.date.available2022-08-23T16:15:51Z
dc.date.issued2007-01-16
dc.date.submitted2008-11-21
dc.identifier.citationScience. 2007 Jan 12;315(5809):230-3. <a href="http://dx.doi.org/10.1126/science.1135344 ">Link to article on publisher's site</a>
dc.identifier.issn1095-9203 (Electronic)
dc.identifier.doi10.1126/science.1135344
dc.identifier.pmid17218525
dc.identifier.urihttp://hdl.handle.net/20.500.14038/34191
dc.description.abstractalphabeta and gammadelta T cells originate from a common, multipotential precursor population in the thymus, but the molecular mechanisms regulating this lineage-fate decision are unknown. We have identified Sox13 as a gammadelta-specific gene in the immune system. Using Sox13 transgenic mice, we showed that this transcription factor promotes gammadelta T cell development while opposing alphabeta T cell differentiation. Conversely, mice deficient in Sox13 expression exhibited impaired development of gammadelta T cells but not alphabeta T cells. One mechanism of SOX13 function is the inhibition of signaling by the developmentally important Wnt/T cell factor (TCF) pathway. Our data thus reveal a dominant pathway regulating the developmental fate of these two lineages of T lymphocytes.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=17218525&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1126/science.1135344
dc.subjectAnimals; Antigens, CD4; Autoantigens; Cell Line; Cell Lineage; Cell Proliferation; Embryonic Development; Gene Expression Profiling; Gene Expression Regulation; Gene Rearrangement, T-Lymphocyte; High Mobility Group Proteins; Humans; *Lymphopoiesis; Mice; Mice, Transgenic; Receptors, Antigen, T-Cell, alpha-beta; Receptors, Antigen, T-Cell, gamma-delta; Signal Transduction; T Cell Transcription Factor 1; T-Lymphocyte Subsets; Wnt Proteins
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleRegulation of gammadelta versus alphabeta T lymphocyte differentiation by the transcription factor SOX13
dc.typeJournal Article
dc.source.journaltitleScience (New York, N.Y.)
dc.source.volume315
dc.source.issue5809
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/849
dc.identifier.contextkey670505
html.description.abstract<p>alphabeta and gammadelta T cells originate from a common, multipotential precursor population in the thymus, but the molecular mechanisms regulating this lineage-fate decision are unknown. We have identified Sox13 as a gammadelta-specific gene in the immune system. Using Sox13 transgenic mice, we showed that this transcription factor promotes gammadelta T cell development while opposing alphabeta T cell differentiation. Conversely, mice deficient in Sox13 expression exhibited impaired development of gammadelta T cells but not alphabeta T cells. One mechanism of SOX13 function is the inhibition of signaling by the developmentally important Wnt/T cell factor (TCF) pathway. Our data thus reveal a dominant pathway regulating the developmental fate of these two lineages of T lymphocytes.</p>
dc.identifier.submissionpathgsbs_sp/849
dc.contributor.departmentDepartment of Pathology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages230-3


This item appears in the following Collection(s)

Show simple item record