Recent advances in endotoxin tolerance

肿瘤坏死因子α 促炎细胞因子 趋化因子 免疫学 脂多糖 下调和上调 炎症 细胞因子 信号转导 败血症 生物 医学 细胞生物学 生物化学 基因
作者
Dan Liu,Shousong Cao,Yejiang Zhou,Yuxia Xiong
出处
期刊:Journal of Cellular Biochemistry [Wiley]
卷期号:120 (1): 56-70 被引量:81
标识
DOI:10.1002/jcb.27547
摘要

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.
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
L756561205完成签到,获得积分10
1秒前
科目三应助阳光思萱采纳,获得10
1秒前
1秒前
huxiaowen发布了新的文献求助10
1秒前
炙热的宛完成签到,获得积分10
1秒前
2秒前
2秒前
木森完成签到,获得积分10
2秒前
3秒前
3秒前
慕青应助Ai采纳,获得10
3秒前
Jasen发布了新的文献求助10
3秒前
3秒前
3秒前
浊人完成签到,获得积分20
4秒前
4秒前
隐形曼青应助Research采纳,获得30
5秒前
5秒前
6秒前
fwx1997发布了新的文献求助10
6秒前
6秒前
潇洒夜安完成签到,获得积分10
7秒前
吐泡泡发布了新的文献求助10
7秒前
NexusExplorer应助yanglj采纳,获得10
7秒前
丑麒发布了新的文献求助10
7秒前
NNi发布了新的文献求助10
8秒前
8秒前
复活完成签到,获得积分10
8秒前
科研通AI6.4应助桃桃好困采纳,获得10
8秒前
yhuang完成签到,获得积分10
9秒前
简单酬海发布了新的文献求助10
9秒前
9秒前
NexusExplorer应助111采纳,获得10
9秒前
fancycow发布了新的文献求助10
9秒前
10秒前
10秒前
金新皓发布了新的文献求助10
10秒前
11秒前
11秒前
温暖的山槐完成签到,获得积分10
11秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
日本現代怪異事典 副読本 700
悉尼大学博士学位论文,题目:Modelling and testing of one-sided stitched laminated composites. 作者:Kristopher P. Plain 650
Machine Learning for Asset Management and Pricing 600
Numerical analysis of the coupled atmosphere-ocean models (CAO II). II 600
Models for the coupled atmosphere and ocean 600
Évora na Idade Média 555
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7385931
求助须知:如何正确求助?哪些是违规求助? 8992669
关于积分的说明 19131765
捐赠科研通 7023169
什么是DOI,文献DOI怎么找? 3227650
关于科研通互助平台的介绍 2390547
邀请新用户注册赠送积分活动 2208865