The Power of Single-Cell Analysis for the Study of Liver Pathobiology

被引:19
作者
Chu, Angela L. [1 ,2 ]
Schilling, Joel D. [3 ,4 ]
King, Kevin R. [5 ,6 ]
Feldstein, Ariel E. [1 ,2 ]
机构
[1] Univ Calif San Diego, Dept Pediat, San Diego, CA 92103 USA
[2] Rady Childrens Hosp, San Diego, CA USA
[3] Washington Univ, Sch Med, Dept Med, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Pathol & Immunol, St Louis, MO USA
[5] Univ Calif San Diego, Dept Cardiol, San Diego, CA 92103 USA
[6] Univ Calif San Diego, Dept Bioengn, San Diego, CA 92103 USA
关键词
GENOME-WIDE EXPRESSION; NUCLEUS RNA-SEQ; SPATIAL RECONSTRUCTION; GENE-EXPRESSION; DISEASE; MYOFIBROBLASTS; LANDSCAPE; CHROMATIN; ORIGIN;
D O I
10.1002/hep.31485
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Single cell transcriptomics has emerged as a powerful lens through which to study the molecular diversity of complex tissues such as the liver, during health and disease, both in animal models and in humans. The earliest gene expression methods measured bulk tissue RNA, but the results were often confusing because they derived from the combined transcriptomes of many different cell types in unknown proportions. To better delineate cell-type-specific expression, investigators developed cell isolation, purification, and sorting protocols, yet still, the RNA derived from ensembles of cells obscured recognition of cellular heterogeneity. Profiling transcriptomes at the single-cell level has opened the door to analyses that were not possible in the past. In this review, we discuss the evolution of single cell transcriptomics and how it has been applied for the study of liver physiology and pathobiology to date.
引用
收藏
页码:437 / 448
页数:12
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