Kranz David M
Department of Biochemistry, University of Illinois 600 South Mathews Avenue, Urbana-Champaign, IL 61801 USA.
F1000 Biol Rep. 2009 Jul 27;1:55. doi: 10.3410/B1-55.
In recent studies, two distinct mechanisms have been proposed to account for major histocompatibility complex (MHC) restriction of T-cell activity: (a) evolution-driven interactions between T-cell receptor (TCR) variable regions and MHC, and (b) a requirement for CD4 or CD8 binding to MHC to initiate signalling through the TCR complex. Both mechanisms are likely to be essential, but for different reasons.
在最近的研究中,已提出两种不同的机制来解释T细胞活性的主要组织相容性复合体(MHC)限制:(a)T细胞受体(TCR)可变区与MHC之间由进化驱动的相互作用,以及(b)CD4或CD8与MHC结合以启动通过TCR复合体的信号传导的需求。这两种机制可能都是必不可少的,但原因不同。