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含 TIR 的衔接蛋白在 Toll 样受体信号通路中的作用。

TIR-containing adaptors in Toll-like receptor signalling.

机构信息

Centre for Innate Immunity and Infectious Diseases, Monash Institute of Medical Research, Monash University, Clayton, Vic., Australia.

出版信息

Cytokine. 2010 Mar;49(3):237-44. doi: 10.1016/j.cyto.2009.01.009. Epub 2009 Mar 4.

Abstract

While the Toll-like receptors (TLRs) are responsible for the recognition and response to pathogen ligands, increasing evidence suggests that the family of five cytosolic Toll/IL-1 receptor (TIR) adaptor proteins also play a crucial role in the specificity of the response. Genetic studies in mice, and increasingly in human polymorphic populations, have given us a greater understanding the role these adaptors play in orchestrating and coordinating the multifaceted immune response to multiple exogenous threats. Importantly, with growing evidence of the critical role TLRs play in responses to host danger signals and autoimmune disease, a more comprehensive understanding and appreciation of the role these adaptors play in disease progression may provide future targets for therapeutic intervention in human disease. Importantly, growing evidence supports the concept of pathway specific and inflammatory control by a better understanding of how these adaptors interact with other signalling mediators, where they localise within the cell and the inflammatory programs they initiate as a way of manipulating immune responses. This review deals with our current understanding of these TIR-containing adaptor proteins and how mutagenesis of specific residues and domains has increased our knowledge of their function in TLR immune responses.

摘要

虽然 Toll 样受体 (TLRs) 负责识别和响应病原体配体,但越来越多的证据表明,五种胞质 Toll/IL-1 受体 (TIR) 衔接蛋白家族在反应的特异性中也起着至关重要的作用。在小鼠中的遗传研究,以及在人类多态性群体中的研究越来越多,使我们更好地理解了这些衔接蛋白在协调和协调对多种外源威胁的多方面免疫反应中的作用。重要的是,随着越来越多的证据表明 TLR 在对宿主危险信号和自身免疫性疾病的反应中起着关键作用,更全面地理解和认识这些衔接蛋白在疾病进展中的作用可能为人类疾病的治疗干预提供未来的靶点。重要的是,越来越多的证据支持通过更好地了解这些衔接子如何与其他信号转导介质相互作用、它们在细胞内的定位以及它们启动的炎症程序来控制特定途径和炎症的概念,以此来操纵免疫反应。这篇综述讨论了我们对这些含 TIR 的衔接蛋白的现有认识,以及特定残基和结构域的诱变如何增加我们对它们在 TLR 免疫反应中的功能的了解。

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