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CD4和CD8的结构视图。

A structural view of CD4 and CD8.

作者信息

Leahy D J

机构信息

Department of Biophysics and Biophysical Chemistry, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205.

出版信息

FASEB J. 1995 Jan;9(1):17-25. doi: 10.1096/fasebj.9.1.7821755.

Abstract

CD4 and CD8 are cell-surface glycoproteins that participate in molecular complexes involved in both T cell development and antigen recognition by T cells. CD4 and CD8 interact with nonpolymorphic regions of class II and class I major histocompatibility complex (MHC) molecules, respectively, and these interactions result in increased intercellular adhesion and enhanced stimulation of T cells. A src-like tyrosine kinase, p56lck, is associated with the cytoplasmic domain of both CD4 and CD8 and may be involved in transmembrane signaling. Crystal structures of extracellular regions of CD4 and CD8 have been determined and have provided a basis for understanding and probing CD4 and CD8 function. The structures of CD4 and CD8 are reviewed here, along with the implications of these structures for CD4 and CD8 function.

摘要

CD4和CD8是细胞表面糖蛋白,它们参与了与T细胞发育和T细胞抗原识别相关的分子复合物。CD4和CD8分别与II类和I类主要组织相容性复合体(MHC)分子的非多态性区域相互作用,这些相互作用导致细胞间粘附增加以及T细胞刺激增强。一种src样酪氨酸激酶p56lck与CD4和CD8的胞质结构域相关联,可能参与跨膜信号传导。已确定CD4和CD8胞外区域的晶体结构,为理解和探究CD4和CD8的功能提供了基础。本文综述了CD4和CD8的结构,以及这些结构对CD4和CD8功能的影响。

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