免疫系统
外周血
败血症
免疫学
剧目
生物
核糖核酸
外围设备
细胞
医学
遗传学
基因
内科学
声学
物理
作者
Lijun Wang,Yao Xiao,Xiaoyong Zhang,Kai Zhu,Wanyi Chen,Zhao Lian,Qing‐Jie Zhao,Hong Zhou,Gan Chen
标识
DOI:10.1016/j.bbrc.2024.150751
摘要
Sepsis is a potentially fatal condition arising from an abnormal immune response to an infection, which can result in organ failure and even death. To explore the mechanism underlying the dysregulated immune response during sepsis and identify potential therapeutic targets, single-cell RNA sequencing (scRNA-seq) and immune repertoire analysis were conducted to depict the cellular landscape of peripheral blood cells in septic mice. We observed significant alterations in the number and proportion of peripheral blood cell populations driven by sepsis. By combining single-cell gene expression profiles and B cell receptor (BCR) repertoire analysis, we discerned that infection inflicted serious damage on the antigen presentation ability of B cells and the diversity of BCR in a short time. In addition, we found that the cecal ligation and puncture procedure in mice inhibited the communication signals of CD4
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