败血症
细胞
转录组
骨骼肌
重症监护室
医学
生物信息学
生物
免疫学
重症监护医学
内科学
基因
基因表达
遗传学
作者
Yanyan Tao,Lijie Song,Heng Xiao,Cheng Liu
出处
期刊:Human gene
[Elsevier BV]
日期:2023-11-04
卷期号:38: 201236-201236
被引量:2
标识
DOI:10.1016/j.humgen.2023.201236
摘要
Sepsis is a severe inflammatory response syndrome caused by infection, which remains a leading cause of morbidity and mortality in the intensive care unit(ICU) patients. Muscle dysfunction is a crucial feature of sepsis. In this study, we employed single-cell transcriptomics sequencing (scRNA-seq) to analyze cell-cell communications in skeletal muscle , aiming to gain a better understanding of the mechanisms involved in sepsis. The results revealed a significant reduction in both the number and strength of cellular communications in sepsis, along with alterations in several pathways, particularly in dendritic cells (DCs). Notably, three pathways—Tnf-Tnfrsf1a, ltgb2-lcam2, and Cd209a-Ceacam1—were significantly changed in sepsis. Our study offers a novel perspective on the mechanisms of muscle dysregulation and clinical treatment for sepsis.
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