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,Carey N. Lumeng,Beiyan Zhou,Qi Ling,Adriana Huertas‐Vázquez,Aldons J. Lusis,Xiaocai Xu,Siming Li,Yonghao Yu,Jun Z. Li,Jiandie D. Lin
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.