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dc.contributor.authorKang, Joonsoo
dc.contributor.authorDiBenedetto, Brian
dc.contributor.authorNarayan, Kavitha
dc.contributor.authorZhao, Hang
dc.contributor.authorDer, Sandy D.
dc.contributor.authorChambers, Cynthia A.
dc.date2022-08-11T08:08:59.000
dc.date.accessioned2022-08-23T16:14:46Z
dc.date.available2022-08-23T16:14:46Z
dc.date.issued2004-08-06
dc.date.submitted2008-10-09
dc.identifier.citation<p>J Immunol. 2004 Aug 15;173(4):2307-14.</p>
dc.identifier.issn0022-1767 (Print)
dc.identifier.doi10.4049/jimmunol.173.4.2307
dc.identifier.pmid15294943
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33939
dc.description.abstractDiverse cytokines necessary for normal lymphopoiesis and lymphocyte homeostasis activate STAT5 in responder cells. Although STAT5 has been suggested to be a central molecular effecter of IL-7 function, its essential role during IL-7-dependent T cell development in vivo remained unclear. Using Stat5(-/-) mice we now show that STAT5 is essential for various functions ascribed to IL-7 in vivo. STAT5 is required for embryonic thymocyte production, TCRgamma gene transcription, and Peyer's patch development. In sharp contrast, normal STAT5 is dispensable for adult thymopoiesis. In peripheral lymphocytes, STAT5 is primarily required for the generation and/or maintenance of gammadelta T cells and TCRgammadelta(+) intraepithelial lymphocytes. Collectively, these results demonstrate that STAT5 is critical for many, but not all, aspects of steady state lymphoid lineage development and maintenance and suggest the existence of previously undocumented cytokine signaling traits and/or cytokine milieu during adult thymopoiesis.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=15294943&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.4049/jimmunol.173.4.2307
dc.subjectAnimals; Cells, Cultured; DNA-Binding Proteins; Flow Cytometry; Gene Rearrangement; Genes, T-Cell Receptor gamma; Immunohistochemistry; Interleukin-7; *Lymphopoiesis; Mice; *Milk Proteins; Peyer's Patches; Polymerase Chain Reaction; Receptors, Interleukin-7; STAT5 Transcription Factor; T-Lymphocytes; Thymus Gland; Trans-Activators; Transcription, Genetic
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleSTAT5 is required for thymopoiesis in a development stage-specific manner
dc.typeJournal Article
dc.source.journaltitleJournal of immunology (Baltimore, Md. : 1950)
dc.source.volume173
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/591
dc.identifier.contextkey646776
html.description.abstract<p>Diverse cytokines necessary for normal lymphopoiesis and lymphocyte homeostasis activate STAT5 in responder cells. Although STAT5 has been suggested to be a central molecular effecter of IL-7 function, its essential role during IL-7-dependent T cell development in vivo remained unclear. Using Stat5(-/-) mice we now show that STAT5 is essential for various functions ascribed to IL-7 in vivo. STAT5 is required for embryonic thymocyte production, TCRgamma gene transcription, and Peyer's patch development. In sharp contrast, normal STAT5 is dispensable for adult thymopoiesis. In peripheral lymphocytes, STAT5 is primarily required for the generation and/or maintenance of gammadelta T cells and TCRgammadelta(+) intraepithelial lymphocytes. Collectively, these results demonstrate that STAT5 is critical for many, but not all, aspects of steady state lymphoid lineage development and maintenance and suggest the existence of previously undocumented cytokine signaling traits and/or cytokine milieu during adult thymopoiesis.</p>
dc.identifier.submissionpathgsbs_sp/591
dc.contributor.departmentDepartment of Pathology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages2307-14


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