Altered T cell receptor signaling and disrupted T cell development in mice lacking Itk

被引:269
作者
Liao, XC
Littman, DR
机构
[1] UNIV CALIF SAN FRANCISCO, DEPT BIOCHEM & BIOPHYS, SAN FRANCISCO, CA 94143 USA
[2] NYU, MED CTR,SKIRBALL INST BIOMOLEC MED, HOWARD HUGHES MED INST,MOLEC PATHOGENESIS PROGRAM, NEW YORK, NY 10016 USA
关键词
D O I
10.1016/1074-7613(95)90065-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Itk is a T cell protein tyrosine kinase (PTK) that, along with Btk and Tee, belongs to a family of cytoplasmic PTKs with N-terminal pleckstrin homology domains. Btk plays a critical role in B lymphocyte development. To determine whether Itk has an analogous role in T lymphocytes, we used gene targeting to prepare mice lacking expression of Itk. Such animals had decreased numbers of mature thymocytes, an effect most clearly observed in mice expressing T cell receptor (TCR) transgenes. Mature T cells from Itk-deficient mice had reduced proliferative responses to allogeneic MHC stimulation and to anti-TCR cross-linking, but responded normally to stimulation with phorbol ester plus ionomycin or with IL-2. These results provide genetic evidence that Itk is involved in T cell development and also suggest that Itk has an important role in proximal events in TCR-mediated signaling pathways.
引用
收藏
页码:757 / 769
页数:13
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