肾
肾脏疾病
单核细胞
可药性
效应器
急性肾损伤
人口
巨噬细胞
生物
炎症
免疫学
癌症研究
医学
内科学
基因
体外
环境卫生
生物化学
作者
Weijian Yao,Ying Chen,Zehua Li,Jing Ji,A‐Bin You,Shanzhao Jin,Yuan Ma,Youlu Zhao,Jinwei Wang,Lei Qu,Hui Wang,Chengang Xiang,Suxia Wang,Gang Liu,Fan Bai,Li Yang
标识
DOI:10.1002/advs.202103675
摘要
Acute kidney injury (AKI) is a complex clinical disorder associated with poor outcomes. Targeted regulation of the degree of inflammation has been a potential strategy for AKI management. Macrophages are the main effector cells of kidney inflammation. However, macrophage heterogeneity in ischemia reperfusion injury induced AKI (IRI-AKI) remains unclear. Using single-cell RNA sequencing of the mononuclear phagocytic system in the murine IRI model, the authors demonstrate the complementary roles of kidney resident macrophages (KRMs) and monocyte-derived infiltrated macrophages (IMs) in modulating tissue inflammation and promoting tissue repair. A unique population of S100a9
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