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CD8α'在CD4与CD8谱系选择中的作用。

The role of CD8 alpha' in the CD4 versus CD8 lineage choice.

作者信息

Salmon P, Mong M, Kang X J, Cado D, Robey E

机构信息

Department of Molecular and Cell Biology, University of California, Berkeley 94720, USA.

出版信息

J Immunol. 1999 Nov 15;163(10):5312-8.

Abstract

During thymic development the recognition of MHC proteins by developing thymocytes influences their lineage commitment, such that recognition of class I MHC leads to CD8 T cell development, whereas recognition of class II MHC leads to CD4 T cell development. The coreceptors CD8 and CD4 may contribute to these different outcomes through interactions with class I and class II MHC, respectively, and through interactions with the tyrosine kinase p56lck (Lck) via their cytoplasmic domains. In this paper we provide evidence that an alternatively spliced form of CD8 that cannot interact with Lck (CD8 alpha') can influence the CD4 vs CD8 lineage decision. Constitutive expression of a CD8 minigene transgene that encodes both CD8 alpha and CD8 alpha' restores CD8 T cell development in CD8 alpha mutant mice, but fails to permit the development of mismatched CD4 T cells bearing class I-specific TCRs. These results indicate that CD8 alpha' favors the development of CD8-lineage T cells, perhaps by reducing Lck activity upon class I MHC recognition in the thymus.

摘要

在胸腺发育过程中,发育中的胸腺细胞对MHC蛋白的识别会影响它们的谱系定向,即对I类MHC的识别会导致CD8 T细胞的发育,而对II类MHC的识别会导致CD4 T细胞的发育。共受体CD8和CD4可能分别通过与I类和II类MHC相互作用,以及通过其胞质结构域与酪氨酸激酶p56lck(Lck)相互作用,促成这些不同的结果。在本文中,我们提供证据表明,一种不能与Lck相互作用的CD8可变剪接形式(CD8α')能够影响CD4与CD8谱系的决定。编码CD8α和CD8α'的CD8小基因转基因的组成型表达可恢复CD8α突变小鼠中CD8 T细胞的发育,但不能使带有I类特异性TCR的错配CD4 T细胞发育。这些结果表明,CD8α'可能通过降低胸腺中I类MHC识别时的Lck活性,促进CD8谱系T细胞的发育。

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