Endothelial cell dynamics in sepsis-induced acute lung injury and acute respiratory distress syndrome: pathogenesis and therapeutic implications

急性呼吸窘迫综合征 败血症 医学 间质细胞 免疫学 发病机制 免疫系统 癌症研究 内科学
作者
Xinyu Qiao,Junhao Yin,Zhihuan Zheng,Liangge Li,Xiujing Feng
出处
期刊:Cell Communication and Signaling [BioMed Central]
卷期号:22 (1): 241-241 被引量:137
标识
DOI:10.1186/s12964-024-01620-y
摘要

Sepsis, a prevalent critical condition in clinics, continues to be the leading cause of death from infections and a global healthcare issue. Among the organs susceptible to the harmful effects of sepsis, the lungs are notably the most frequently affected. Consequently, patients with sepsis are predisposed to developing acute lung injury (ALI), and in severe cases, acute respiratory distress syndrome (ARDS). Nevertheless, the precise mechanisms associated with the onset of ALI/ARDS remain elusive. In recent years, there has been a growing emphasis on the role of endothelial cells (ECs), a cell type integral to lung barrier function, and their interactions with various stromal cells in sepsis-induced ALI/ARDS. In this comprehensive review, we summarize the involvement of endothelial cells and their intricate interplay with immune cells and stromal cells, including pulmonary epithelial cells and fibroblasts, in the pathogenesis of sepsis-induced ALI/ARDS, with particular emphasis placed on discussing the several pivotal pathways implicated in this process. Furthermore, we discuss the potential therapeutic interventions for modulating the functions of endothelial cells, their interactions with immune cells and stromal cells, and relevant pathways associated with ALI/ARDS to present a potential therapeutic strategy for managing sepsis and sepsis-induced ALI/ARDS.
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
等你下课完成签到 ,获得积分10
刚刚
唯有一个心完成签到,获得积分10
刚刚
YanJinyu完成签到,获得积分10
刚刚
CFD应助科研通管家采纳,获得10
刚刚
小蘑菇应助能能鹤采纳,获得10
刚刚
汪金完成签到,获得积分10
刚刚
线呢完成签到 ,获得积分10
1秒前
田様应助科研通管家采纳,获得10
1秒前
1秒前
科研通AI2S应助zwr采纳,获得10
1秒前
小黑发布了新的文献求助10
1秒前
1秒前
1秒前
1秒前
1秒前
2秒前
2秒前
2秒前
舒适的青烟完成签到,获得积分10
2秒前
li发布了新的文献求助10
2秒前
乔恩的猫完成签到,获得积分10
2秒前
2秒前
3秒前
3秒前
小明发布了新的文献求助10
3秒前
pufferfish完成签到,获得积分10
3秒前
阿呷惹完成签到,获得积分10
4秒前
vivre223完成签到,获得积分10
4秒前
4秒前
5秒前
英俊的铭应助wj采纳,获得10
5秒前
柠溪完成签到 ,获得积分10
5秒前
nako7575完成签到,获得积分10
5秒前
Driscoll完成签到 ,获得积分10
5秒前
5秒前
cdercder应助潇洒的惋清采纳,获得10
5秒前
害怕的水之完成签到,获得积分10
6秒前
桐桐应助潇洒的惋清采纳,获得10
6秒前
cdercder应助潇洒的惋清采纳,获得10
6秒前
6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
Prompt Engineering for Clinicians: Harnessing AI in Everyday Medical Practice 600
University Physics for the Life Sciences 500
REAL-WORLD EFFICACY AND GENOMIC LANDSCAPE OF POLATUZUMA VEDOTIN-BASED FIRST-LINE THERAPY IN DIFFUSE LARGE B-CELL LYMPHOMA: A FOCUS ON TP53 MUTATIONS AND TREATMENT RESPONSE 500
Handbook of Luminescence Dating 500
Safety Pharmacology 500
《KNN基无铅压电陶瓷电学性能优化与物理机理研究》 500
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 计算机科学 化学工程 生物化学 物理 内科学 复合材料 催化作用 光电子学 物理化学 电极 细胞生物学 基因 遗传学
热门帖子
关注 科研通微信公众号,转发送积分 6952187
求助须知:如何正确求助?哪些是违规求助? 8636402
关于积分的说明 18312965
捐赠科研通 6395121
什么是DOI,文献DOI怎么找? 3082313
关于科研通互助平台的介绍 2127808
邀请新用户注册赠送积分活动 2059206