| Literature DB >> 19415629 |
Mohamad Azhar1, Moying Yin, Ramireddy Bommireddy, John J Duffy, Junqi Yang, Sharon A Pawlowski, Gregory P Boivin, Sandra J Engle, L P Sanford, Christina Grisham, Ram R Singh, George F Babcock, Thomas Doetschman.
Abstract
Transforming growth factor beta1 (TGFbeta1) is a multifunctional growth factor involved in wound healing, tissue fibrosis, and in the pathogenesis of many syndromic diseases (e.g., Marfan syndrome, Camurati-Engelmann disease) and muscular, neurological, ophthalmic, cardiovascular and immunological disorders, and cancer. Since the generation of Tgfb1 knockout mice, there has been extraordinary progress in understanding its physiological and pathophysiological function. Here, we report the generation of a conditional knockout allele for Tgfb1 in which its exon 6 is flanked with LoxP sites. As proof of principle, we crossed these mice to LckCre transgenic mice and specifically disrupted Tgfb1 in T cells. The results indicate that T-cell-produced TGFbeta1 is required for normal in vivo regulation of peripheral T-cell activation, maintenance of T-cell homeostasis, and suppression of autoimmunity. Copyright 2009 Wiley-Liss, Inc.Entities:
Mesh:
Substances:
Year: 2009 PMID: 19415629 PMCID: PMC2766615 DOI: 10.1002/dvg.20516
Source DB: PubMed Journal: Genesis ISSN: 1526-954X Impact factor: 2.487