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T cell integrin overexpression as a model of murine autoimmunity
Authors:Raymond?L.?Yung  author-information"  >  author-information__contact u-icon-before"  >  mailto:ryung@umich.edu"   title="  ryung@umich.edu"   itemprop="  email"   data-track="  click"   data-track-action="  Email author"   data-track-label="  "  >Email author,Donna?Ray,Ru?Ran?Mo,Jun?Chen
Affiliation:(1) Department of Internal Medicine, University of Michigan, 48109-0940 Ann Arbor, MI, USA;(2) Divisions of Geriatrics and Rheumatology, Department of Internal Medicine, University of Michigan, 1500 East Medical Center Drive, 48109-0940 Ann Arbor, MI, USA
Abstract:Integrin adhesion molecules have important adhesion and signaling functions. They also play a central role in the pathogenesis of many autoimmune diseases. Over the past few years we have described a T cell adoptive transfer model to investigate the role of T cell integrin adhesion molecules in the development of autoimmunity. This report summarizes the methods we used in establishing this murine model. By treating murine CD4+ T cells with DNA hypomethylating agents and by transfection we were able to test thein vitro effects of integrin overexpression on T cell autoreactive proliferation, cytotoxicity, adhesion and trafficking. Furthermore, we showed that the ability to inducein vivo autoimmunity may be unique to the integrin lymphocyte function associated antigen-1 (LFA-1). Published: October 24, 2003
Keywords:  KeywordHeading"  >Indexing terms Integrins  DNA methylation
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