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TIRAP、TRAM 和 Toll 样受体:不为人知的故事。

TIRAP, TRAM, and Toll-Like Receptors: The Untold Story.

机构信息

Department of Immunology and Cell Biology, Cancer Research Institute, Faculty of Medicine and Health Sciences, Université de Sherbrooke, Sherbrooke, Québec, Canada.

出版信息

Mediators Inflamm. 2023 Mar 7;2023:2899271. doi: 10.1155/2023/2899271. eCollection 2023.

Abstract

Toll-like receptors (TLRs) are the most studied receptors among the pattern recognition receptors (PRRs). They act as microbial sensors, playing major roles in the regulation of the innate immune system. TLRs mediate their cellular functions through the activation of MyD88-dependent or MyD88-independent signaling pathways. Myd88, or myeloid differentiation primary response 88, is a cytosolic adaptor protein essential for the induction of proinflammatory cytokines by all TLRs except TLR3. While the crucial role of Myd88 is well described, the contribution of other adaptors in mediating TLR signaling and function has been underestimated. In this review, we highlight important results demonstrating that TIRAP and TRAM adaptors are also required for full signaling activity and responses induced by most TLRs.

摘要

Toll 样受体 (TLRs) 是模式识别受体 (PRRs) 中研究最多的受体。它们作为微生物传感器,在调节先天免疫系统中发挥着重要作用。TLRs 通过激活 MyD88 依赖性或 MyD88 非依赖性信号通路来发挥其细胞功能。MyD88(髓样分化初级反应 88)是一种胞质衔接蛋白,对于除 TLR3 以外的所有 TLR 诱导促炎细胞因子的产生都是必不可少的。虽然 MyD88 的关键作用已得到充分描述,但其他衔接蛋白在介导 TLR 信号转导和功能方面的作用却被低估了。在这篇综述中,我们强调了一些重要的结果,这些结果表明 TIRAP 和 TRAM 衔接蛋白对于大多数 TLR 诱导的完全信号活性和反应也是必需的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1b6c/10014160/ca402b2071fb/MI2023-2899271.001.jpg

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