肝星状细胞
间充质
肝小叶
细胞生物学
肝纤维化
生物
病理
转录组
纤维化
肌成纤维细胞
间充质干细胞
基因表达
医学
基因
生物化学
作者
Ross Dobie,John R. Wilson‐Kanamori,Beth E. P. Henderson,James R. Smith,Kylie P. Matchett,Jordan R. Portman,Karolina Wallenborg,Simone Picelli,Anna Zagórska,Swetha Pendem,Thomas E. Hudson,Minnie M. Wu,Grant R. Budas,David G. Breckenridge,Ewen M. Harrison,Damian J. Mole,Stephen J. Wigmore,Prakash Ramachandran,Chris P. Ponting,Sarah A. Teichmann
出处
期刊:Cell Reports
[Cell Press]
日期:2019-11-01
卷期号:29 (7): 1832-1847.e8
被引量:317
标识
DOI:10.1016/j.celrep.2019.10.024
摘要
Iterative liver injury results in progressive fibrosis disrupting hepatic architecture, regeneration potential, and liver function. Hepatic stellate cells (HSCs) are a major source of pathological matrix during fibrosis and are thought to be a functionally homogeneous population. Here, we use single-cell RNA sequencing to deconvolve the hepatic mesenchyme in healthy and fibrotic mouse liver, revealing spatial zonation of HSCs across the hepatic lobule. Furthermore, we show that HSCs partition into topographically diametric lobule regions, designated portal vein-associated HSCs (PaHSCs) and central vein-associated HSCs (CaHSCs). Importantly we uncover functional zonation, identifying CaHSCs as the dominant pathogenic collagen-producing cells in a mouse model of centrilobular fibrosis. Finally, we identify LPAR1 as a therapeutic target on collagen-producing CaHSCs, demonstrating that blockade of LPAR1 inhibits liver fibrosis in a rodent NASH model. Taken together, our work illustrates the power of single-cell transcriptomics to resolve the key collagen-producing cells driving liver fibrosis with high precision.
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