What's the Catch? The Significance of Catch Bonds in T Cell Activation

被引:6
|
作者
Faust, Michael A. [1 ]
Rase, Viva J. [1 ]
Lamb, Tracey J. [1 ]
Evavold, Brian D. [1 ]
机构
[1] Univ Utah, Dept Pathol, Div Microbiol & Immunol, Salt Lake City, UT USA
来源
JOURNAL OF IMMUNOLOGY | 2023年 / 211卷 / 03期
基金
美国国家卫生研究院;
关键词
SELECTIN GLYCOPROTEIN LIGAND-1; ALTERED PEPTIDE LIGANDS; SIGNAL-TRANSDUCTION; RECEPTOR AFFINITY; STRUCTURAL BASIS; TCR AFFINITY; KINETICS; INTEGRIN; ADHESION; BINDING;
D O I
10.4049/jimmunol.2300141
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
One of the main goals in T cell biology has been to investigate how TCR recognition of peptide:MHC (pMHC) determines T cell phenotype and fate. Ag recognition is required to facilitate survival, expansion, and effector function of T cells. Historically, TCR affinity for pMHC has been used as a predictor for T cell fate and responsiveness, but there have now been several examples of nonfunctional high-affinity clones and low-affinity highly functional clones. Recently, more attention has been paid to the TCR being a mechanoreceptor where the key biophysical determinant is TCR bond lifetime under force. As outlined in this review, the fundamental parameters between the TCR and pMHC that control Ag recognition and T cell triggering are affinity, bond lifetime, and the amount of force at which the peak lifetime occurs.
引用
收藏
页码:333 / 342
页数:10
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