T cell Receptor Signal Transduction in T lymphocytes.

T cell Receptor Signal Transduction in T lymphocytes.
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DOI:
10.4172/2155-9899.s12-005
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发表时间:
2012-10-27
期刊:
Journal of clinical & cellular immunology
影响因子:
--
通讯作者:
Zhong XP
Zhong XP
中科院分区:
其他
文献类型:
--
作者:
Gorentla BK;Zhong XP

文献摘要

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T细胞受体(TCR)识别由主要组织相容性复合体(MHC)分子呈递的自身或外来抗原。TCR的参与触发多分子信号体的形成,导致第二信使的产生和随后的多个远端信号级联的激活,例如Ca+2-钙调神经磷酸酶-NFAT、RasGRP 1-Ras-Erk 1/2、PKCθ-IKK-NFκB和TSC 1/2-mTOR通路。这些信号级联控制T细胞生物学的许多方面。已经发展了微调TCR信号传导以维持T细胞稳态和自身耐受性的机制,并适当地对微生物感染产生有效反应。TCR信号传导的缺陷或失调已经涉及多种人类疾病的发病机制。
The T cell receptor (TCR) recognizes self or foreign antigens presented by major histocompatibility complex (MHC) molecules. Engagement of the TCR triggers the formation of multi-molecular signalosomes that lead to the generation of second messengers and subsequent activation of multiple distal signaling cascades, such as the Ca+2-calcineurin-NFAT, RasGRP1-Ras-Erk1/2, PKCθ-IKK-NFκB, and TSC1/2-mTOR pathways. These signaling cascades control many aspects of T cell biology. Mechanisms have been evolved to fine-tune TCR signaling to maintain T cell homeostasis and self-tolerance, and to properly mount effective responses to microbial infection. Defects or deregulation of TCR signaling has been implicated in the pathogenesis of multiple human diseases.