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重新审视血小板和 Toll 样受体 (TLRs):血管免疫与血栓形成的交汇点。

Revisiting Platelets and Toll-Like Receptors (TLRs): At the Interface of Vascular Immunity and Thrombosis.

机构信息

Department of Surgery and Anaesthesia, The University of Otago, Wellington 6021, New Zealand.

Wellington Cardiovascular Research Group, Wellington 6021, New Zealand.

出版信息

Int J Mol Sci. 2020 Aug 26;21(17):6150. doi: 10.3390/ijms21176150.

Abstract

While platelet function has traditionally been described in the context of maintaining vascular integrity, recent evidence suggests that platelets can modulate inflammation in a much more sophisticated and nuanced manner than previously thought. Some aspects of this expanded repertoire of platelet function are mediated via expression of Toll-like receptors (TLRs). TLRs are a family of pattern recognition receptors that recognize pathogen-associated and damage-associated molecular patterns. Activation of these receptors is crucial for orchestrating and sustaining the inflammatory response to both types of danger signals. The TLR family consists of 10 known receptors, and there is at least some evidence that each of these are expressed on or within human platelets. This review presents the literature on TLR-mediated platelet activation for each of these receptors, and the existing understanding of platelet-TLR immune modulation. This review also highlights unresolved methodological issues that potentially contribute to some of the discrepancies within the literature, and we also suggest several recommendations to overcome these issues. Current understanding of TLR-mediated platelet responses in influenza, sepsis, transfusion-related injury and cardiovascular disease are discussed, and key outstanding research questions are highlighted. In summary, we provide a resource-a "researcher's toolkit"-for undertaking further research in the field of platelet-TLR biology.

摘要

虽然血小板功能传统上被描述为维持血管完整性,但最近的证据表明,血小板可以以比以前想象的更为复杂和微妙的方式调节炎症。血小板功能扩展谱的某些方面是通过 Toll 样受体 (TLR) 的表达来介导的。TLR 是一组模式识别受体,可识别病原体相关和损伤相关的分子模式。这些受体的激活对于协调和维持对这两种危险信号的炎症反应至关重要。TLR 家族由 10 个已知的受体组成,至少有一些证据表明,这些受体中的每一个都在人血小板上或内表达。这篇综述介绍了针对这些受体的 TLR 介导的血小板激活的文献,以及对血小板-TLR 免疫调节的现有认识。这篇综述还强调了尚未解决的方法学问题,这些问题可能导致文献中的一些差异,我们还提出了一些建议来克服这些问题。讨论了 TLR 介导的血小板在流感、脓毒症、输血相关损伤和心血管疾病中的反应,强调了关键的未解决研究问题。总之,我们提供了一个资源——一个“研究人员的工具包”——用于在血小板-TLR 生物学领域开展进一步的研究。

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