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内毒素耐受的最新进展。

Recent advances in endotoxin tolerance.

机构信息

Department of Pharmacology, School of Pharmacy, Southwest Medical University, Luzhou, China.

Gastrointestinal Surgery, Affiliated Hospital of Southwest Medical University, Southwest Medical University, Luzhou, China.

出版信息

J Cell Biochem. 2019 Jan;120(1):56-70. doi: 10.1002/jcb.27547. Epub 2018 Sep 23.

Abstract

Endotoxin tolerance is defined as a reduced capacity of a cell to respond endotoxin (lipopolysaccharide, LPS) challenge after an initial encounter with endotoxin in advance. The body becomes tolerant to subsequent challenge with a lethal dose of endotoxin and cytokines release and cell/tissue damage induced by inflammatory reaction are significantly reduced in the state of endotoxin tolerance. The main characteristics of endotoxin tolerance are downregulation of inflammatory mediators such as tumor necrosis factor α (TNF-α), interleukin-1β (IL-1β), and C-X-C motif chemokine 10 (CXCL10) and upregulation of anti-inflammatory cytokines such as IL-10 and transforming growth factor β (TGF-β). Therefore, endotoxin tolerance is often regarded as the regulatory mechanism of the host against excessive inflammation. Endotoxin tolerance is a complex pathophysiological process and involved in multiple cellular signal pathways, receptor alterations, and biological molecules. However, the exact mechanism remains elusive up to date. To better understand the underlying cellular and molecular mechanisms of endotoxin tolerance, it is crucial to investigate the comprehensive cellular signal pathways, signaling proteins, cell surface molecules, proinflammatory and anti-inflammatory cytokines, and other mediators. Endotoxin tolerance plays an important role in reducing the mortality of sepsis, endotoxin shock, and other endotoxin-related diseases. Recent reports indicated that endotoxin tolerance is also related to other diseases such as cystic fibrosis, acute coronary syndrome, liver ischemia-reperfusion injury, and cancer. The aim of this review is to discuss the recent advances in endotoxin tolerance mainly based on the cellular and molecular mechanisms by outline the current state of the knowledge of the involvement of the toll-like receptor 4 (TLR4) signaling pathways, negative regulate factor, microRNAs, apoptosis, chromatin modification, and gene reprogramming of immune cells in endotoxin tolerance. We hope to provide a new idea and scientific basis for the rational treatment of endotoxin-related diseases such as endotoxemia, sepsis, and endotoxin shock clinically.

摘要

内毒素耐受定义为细胞在初次接触内毒素(脂多糖,LPS)后,对随后的内毒素致死剂量的挑战的反应能力降低。在内毒素耐受状态下,细胞/组织损伤引起的细胞因子释放和炎症反应诱导的细胞/组织损伤显著减少。内毒素耐受的主要特征是炎症介质如肿瘤坏死因子 α(TNF-α)、白细胞介素-1β(IL-1β)和 C-X-C 基序趋化因子 10(CXCL10)的下调和抗炎细胞因子如白细胞介素-10(IL-10)和转化生长因子-β(TGF-β)的上调。因此,内毒素耐受通常被认为是宿主对抗过度炎症的调节机制。内毒素耐受是一个复杂的病理生理过程,涉及多个细胞信号通路、受体改变和生物分子。然而,确切的机制至今仍不清楚。为了更好地理解内毒素耐受的潜在细胞和分子机制,研究全面的细胞信号通路、信号蛋白、细胞表面分子、促炎和抗炎细胞因子以及其他介质至关重要。内毒素耐受在降低脓毒症、内毒素休克和其他与内毒素相关疾病的死亡率方面起着重要作用。最近的报告表明,内毒素耐受也与其他疾病有关,如囊性纤维化、急性冠状动脉综合征、肝缺血再灌注损伤和癌症。本综述的目的是讨论内毒素耐受的最新进展,主要基于细胞和分子机制,概述了 Toll 样受体 4(TLR4)信号通路、负调节因子、microRNAs、细胞凋亡、染色质修饰和免疫细胞基因重编程在内毒素耐受中的作用。我们希望为临床上合理治疗内毒素血症、脓毒症和内毒素休克等与内毒素相关的疾病提供新的思路和科学依据。

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