Single-Cell Deconvolution of Fibroblast Heterogeneity in Mouse Pulmonary Fibrosis

被引:389
作者
Xie, Ting [1 ]
Wang, Yizhou [2 ]
Deng, Nan [3 ]
Huang, Guanling [1 ]
Taghavifar, Forough [1 ]
Geng, Yan [1 ]
Liu, Ningshan [1 ]
Kulur, Vrishika [1 ]
Yao, Changfu [1 ]
Chen, Peter [1 ]
Liu, Zhengqiu [3 ]
Stripp, Barry [1 ]
Tang, Jie [2 ]
Liang, Jiurong [1 ]
Noble, Paul W. [1 ]
Jiang, Dianhua [1 ]
机构
[1] Cedars Sinai Med Ctr, Dept Med, Div Pulm & Crit Care Med, Womens Guild Lung Inst, Los Angeles, CA 90048 USA
[2] Cedars Sinai Med Ctr, Dept Biomed Sci, Genom Core, Los Angeles, CA 90048 USA
[3] Cedars Sinai Med Ctr, Samuel Oschin Comprehens Canc Inst, Los Angeles, CA 90048 USA
关键词
HEPATIC STELLATE CELLS; SMOOTH-MUSCLE; MESENCHYMAL LINEAGES; DEVELOPING LUNG; RESIDENT FIBROBLASTS; INTERSTITIAL CELL; MESOTHELIAL CELLS; LIVER FIBROSIS; ADULT LUNG; EXPRESSION;
D O I
10.1016/j.celrep.2018.03.010
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Fibroblast heterogeneity has long been recognized in mouse and human lungs, homeostasis, and disease states. However, there is no common consensus on fibroblast subtypes, lineages, biological properties, signaling, and plasticity, which severely hampers our understanding of the mechanisms of fibrosis. To comprehensively classify fibroblast populations in the lung using an unbiased approach, single-cell RNA sequencing was performed with mesenchymal preparations from either uninjured or bleomycin-treated mouse lungs. Single-cell transcriptome analyses classified and defined six mesenchymal cell types in normal lung and seven in fibrotic lung. Furthermore, delineation of their differentiation trajectory was achieved by a machine learning method. This collection of single-cell transcriptomes and the distinct classification of fibroblast subsets provide a new resource for understanding the fibroblast landscape and the roles of fibroblasts in fibrotic diseases.
引用
收藏
页码:3625 / 3640
页数:16
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