Suppr超能文献

心脏中的白细胞介素18

Interleukin 18 in the heart.

作者信息

Wang Meijing, Markel Troy A, Meldrum Daniel R

机构信息

Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana, USA.

出版信息

Shock. 2008 Jul;30(1):3-10. doi: 10.1097/SHK.0b013e318160f215.

Abstract

IL-18, originally termed as interferon gamma (IFN-gamma) inducing factor, is a proinflammatory cytokine that belongs to the IL-1 cytokine superfamily. IL-18 plays an important role in immune, infectious, and inflammatory diseases due to its induction of IFN-gamma. However, accumulated evidence has demonstrated that other effects of IL-18 are independent of IFN-gamma. Here, we reviewed the current literatures regarding the role of IL-18 in the heart and cardiovascular system. Infiltrated neutrophils, resident macrophages, endothelial cells, smooth muscle cells, and cardiomyocytes in the heart are able to produce IL-18 in response to injury. IL-18 is produced as a biologically inactive precursor (pro-IL-18) that is activated by caspase 1 (the IL-1beta converting enzyme). Elevated IL-18 levels have been observed in cardiac tissue and circulation after myocardial I/R and sepsis. The possible cellular and molecular mechanisms concerning IL-18-induced myocardial injury include induction of inflammation, increased apoptosis, a cardiac hypertrophy effect, modulation of mitogen activated protein kinase activation, and changes in intracellular calcium. Finally, we briefly reviewed the therapeutic strategies for inhibiting IL-18's biological activity to protect cardiac tissue from injury.

摘要

白细胞介素-18(IL-18)最初被称为干扰素γ(IFN-γ)诱导因子,是一种促炎细胞因子,属于白细胞介素-1细胞因子超家族。由于IL-18可诱导IFN-γ,它在免疫、感染和炎症性疾病中发挥着重要作用。然而,越来越多的证据表明,IL-18的其他作用独立于IFN-γ。在此,我们综述了当前关于IL-18在心脏和心血管系统中作用的文献。心脏中浸润的中性粒细胞、驻留巨噬细胞、内皮细胞、平滑肌细胞和心肌细胞在受到损伤时能够产生IL-18。IL-18以无生物活性的前体(前IL-18)形式产生,该前体由半胱天冬酶1(IL-1β转换酶)激活。在心肌缺血/再灌注和脓毒症后,心脏组织和循环中观察到IL-18水平升高。IL-18诱导心肌损伤的可能细胞和分子机制包括炎症诱导、细胞凋亡增加、心脏肥大效应、丝裂原活化蛋白激酶激活的调节以及细胞内钙的变化。最后,我们简要综述了抑制IL-18生物活性以保护心脏组织免受损伤的治疗策略。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验