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CD19 - CR2 - TAPA - 1复合物、CD45与B淋巴细胞抗原受体的信号传导

The CD19-CR2-TAPA-1 complex, CD45 and signaling by the antigen receptor of B lymphocytes.

作者信息

Fearon D T

机构信息

University of Cambridge School of Clinical Medicine, UK.

出版信息

Curr Opin Immunol. 1993 Jun;5(3):341-8. doi: 10.1016/0952-7915(93)90051-s.

Abstract

A paradigm describing the response of T lymphocytes to antigen holds that signals from antigen receptors must be modulated by non-antigen-specific, accessory membrane proteins for an appropriate cellular response to occur, such as differentiation, activation and tolerance. Recent studies suggest that this paradigm applies also to B lymphocytes. Signaling through membrane IgM in these cells requires CD45, a phosphotyrosine phosphatase, and is amplified by a complex containing CD19, complement receptor 2 (CD21), and TAPA-1, which recruits the intracellular enzyme, phosphatidylinositol 3-kinase.

摘要

一种描述T淋巴细胞对抗原反应的模式认为,来自抗原受体的信号必须由非抗原特异性的辅助膜蛋白进行调节,才能发生适当的细胞反应,如分化、激活和耐受。最近的研究表明,这种模式也适用于B淋巴细胞。这些细胞中通过膜IgM的信号传导需要CD45(一种磷酸酪氨酸磷酸酶),并由一个包含CD19、补体受体2(CD21)和TAPA-1的复合物进行放大,该复合物可募集细胞内酶磷脂酰肌醇3激酶。

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