Cell Surface Signaling Molecules in the Control of Immune Responses: A Tide Model

被引:141
作者
Zhu, Yuwen [1 ,2 ]
Yao, Sheng [1 ,2 ]
Chen, Lieping [1 ,2 ]
机构
[1] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06519 USA
[2] Yale Univ, Sch Med, Yale Comprehens Canc Ctr, New Haven, CT 06519 USA
基金
美国国家卫生研究院;
关键词
PATTERN-RECOGNITION RECEPTORS; HERPESVIRUS ENTRY MEDIATOR; CD4(+) T-CELLS; NF-KAPPA-B; COSTIMULATORY MOLECULE; DENDRITIC CELLS; NK-CELLS; NONSELF DISCRIMINATION; IMMUNOLOGICAL SYNAPSE; SUPERFAMILY MEMBERS;
D O I
10.1016/j.immuni.2011.04.008
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A large numbers of cell surface signaling molecules (CSSMs) have been molecularly identified and functionally characterized in recent years and, via these studies, our knowledge in the control of immune response has increased exponentially. Two major lines of evidence emerge. First, the majority of immune cells rely on one or few CSSMs to deliver a primary triggering signal to sense their environment, leading to initiation of an immune response. Second, both costimulatory CSSMs that promote the response, and coinhibitory CSSMs that inhibit the response, are required to control direction and magnitude of a given immune response. With such tight feedback, immune responses are tuned and returned to baseline. These findings extend well beyond our previous observation in the requirement for lymphocyte activation and argue a revisit of the traditional "two-signal model" for activation and tolerance of lymphocytes. Here we propose a "tide" model to accommodate and interpret current experimental findings.
引用
收藏
页码:466 / 478
页数:13
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