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缺乏跨膜和胞外结构域的CD45对TCR信号的调节

Regulation of TCR signaling by CD45 lacking transmembrane and extracellular domains.

作者信息

Volarević S, Niklinska B B, Burns C M, June C H, Weissman A M, Ashwell J D

机构信息

Laboratory of Immune Cell Biology, National Cancer Institute, National Institutes of Health, Bethesda, MD 20892.

出版信息

Science. 1993 Apr 23;260(5107):541-4. doi: 10.1126/science.8475386.

Abstract

The CD45 protein is a transmembrane tyrosine phosphatase that is required for normal T cell receptor (TCR)-mediated signaling. A chimeric complementary DNA encoding the intracellular enzymatically active portion of murine CD45 preceded by a short amino-terminal sequence from p60c-src was transfected into CD45- T cells. Expression of this chimeric protein corrected most of the TCR signaling abnormalities observed in the absence of CD45, including TCR-mediated enhancement of tyrosine kinase activity and Ca2+ flux. Thus, the enzymatically active intracellular portion of CD45 is sufficient to allow TCR transmembrane signaling.

摘要

CD45蛋白是一种跨膜酪氨酸磷酸酶,是正常T细胞受体(TCR)介导的信号传导所必需的。将一个嵌合互补DNA转染到CD45- T细胞中,该嵌合互补DNA编码鼠CD45的细胞内酶活性部分,并在其前面加上来自p60c-src的短氨基末端序列。这种嵌合蛋白的表达纠正了在没有CD45的情况下观察到的大多数TCR信号异常,包括TCR介导的酪氨酸激酶活性增强和Ca2+通量。因此,CD45的具有酶活性的细胞内部分足以实现TCR跨膜信号传导。

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