T细胞受体
CD8型
生物
主要组织相容性复合体
MHC限制
遗传学
MHC I级
生殖系
基因
T细胞
分子生物学
抗原
免疫系统
作者
Bee-Cheng Sim,Loukia Zerva,Mark I. Greene,Nicholas R. J. Gascoigne
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1996-08-16
卷期号:273 (5277): 963-966
被引量:153
标识
DOI:10.1126/science.273.5277.963
摘要
Individual T cell receptor (TCR) V α elements are expressed preferentially in CD4 or CD8 peripheral T cell subsets. The closely related V α 3.1 and V α 3.2 elements show reciprocal selection into CD4 and CD8 subsets, respectively. Transgenic mice expressing site-directed mutants of a V α 3.1 gene were used to show that individual residues in either the complementarity-determining region 1 (CDR1) or CDR2 were sufficient to change selection from the CD4 subset to the CD8 subset. Thus, the germline-encoded V α elements are a major influence on major histocompatibility class complex (MHC) restriction, most likely by a preferential interaction with one or the other class of MHC molecule.
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