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蛋白酶激活受体在心脏先天免疫反应中的作用。

Role of protease-activated receptors for the innate immune response of the heart.

机构信息

Department of Cardiology and Pneumology, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.

Department of Cardiology and Pneumology, Charité-Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.

出版信息

Trends Cardiovasc Med. 2014 Aug;24(6):249-55. doi: 10.1016/j.tcm.2014.06.004. Epub 2014 Jun 27.

Abstract

Protease-activated receptors (PARs) are a family of G-protein-coupled receptors with a unique activation mechanism via cleavage by the serine proteases of the coagulation cascade, immune cell-released proteases, and proteases from pathogens. Pathogens, such as viruses and bacteria, cause myocarditis and heart failure and PAR1 was shown to positively regulate the anti-viral innate immune response via interferon β during virus-induced myocarditis. In contrast, PAR2 negatively regulated the innate immune response and inhibited the interferon β expression. Thus, PARs play a central role for the innate immune response in the heart.

摘要

蛋白酶激活受体(PARs)是一组 G 蛋白偶联受体,其独特的激活机制是通过凝血级联中的丝氨酸蛋白酶、免疫细胞释放的蛋白酶和病原体蛋白酶的切割来实现的。病原体,如病毒和细菌,会导致心肌炎和心力衰竭,研究表明,在病毒诱导的心肌炎中,PAR1 通过干扰素β 正向调节抗病毒固有免疫反应。相比之下,PAR2 负调节固有免疫反应并抑制干扰素β 的表达。因此,PARs 在心脏的固有免疫反应中起着核心作用。

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