生物
肝星状细胞
特雷姆2
串扰
基因
受体
细胞生物学
细胞信号
信号转导
脂肪肝
转录组
细胞
细胞内
遗传学
基因表达
疾病
髓系细胞
内分泌学
内科学
物理
光学
医学
作者
Xuelian Xiong,Henry Kuang,Sahar Ansari,Tongyu Liu,Jianke Gong,Shuai Wang,Xu-Yun Zhao,Yewei Ji,Chuan Li,Liang Guo,Linkang Zhou,Zhimin Chen,Paola León‐Mimila,Meng Ting Chung,Katsuo Kurabayashi,Judy S. Opp,Francisco Campos‐Pérez,Hugo Villamil‐Ramírez,Samuel Canizales‐Quinteros,Robert Lyons
出处
期刊:Molecular Cell
[Elsevier BV]
日期:2019-08-01
卷期号:75 (3): 644-660.e5
被引量:771
标识
DOI:10.1016/j.molcel.2019.07.028
摘要
Cell-cell communication via ligand-receptor signaling is a fundamental feature of complex organs. Despite this, the global landscape of intercellular signaling in mammalian liver has not been elucidated. Here we perform single-cell RNA sequencing on non-parenchymal cells isolated from healthy and NASH mouse livers. Secretome gene analysis revealed a highly connected network of intrahepatic signaling and disruption of vascular signaling in NASH. We uncovered the emergence of NASH-associated macrophages (NAMs), which are marked by high expression of triggering receptors expressed on myeloid cells 2 (Trem2), as a feature of mouse and human NASH that is linked to disease severity and highly responsive to pharmacological and dietary interventions. Finally, hepatic stellate cells (HSCs) serve as a hub of intrahepatic signaling via HSC-derived stellakines and their responsiveness to vasoactive hormones. These results provide unprecedented insights into the landscape of intercellular crosstalk and reprogramming of liver cells in health and disease.
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