全基因组关联研究
生物
慢性阻塞性肺病
清脆的
诱导多能干细胞
基因
电池类型
遗传学
细胞
医学
单核苷酸多态性
基因型
内科学
胚胎干细胞
作者
Rhiannon B. Werder,Tao Liu,Kristine M. Abo,Jonathan Lindstrom-Vautrin,Carlos Villacorta-Martín,Jessie Huang,Anne Hinds,Nathan Boyer,Esther Bullitt,Marc Liesa,Edwin K. Silverman,Darrell N. Kotton,Michael H. Cho,Xiaobo Zhou,Andrew A. Wilson
出处
期刊:Science Advances
[American Association for the Advancement of Science]
日期:2022-07-13
卷期号:8 (28)
被引量:12
标识
DOI:10.1126/sciadv.abo6566
摘要
Genome-wide association studies (GWAS) have identified dozens of loci associated with chronic obstructive pulmonary disease (COPD) susceptibility; however, the function of associated genes in the cell type(s) affected in disease remains poorly understood, partly due to a lack of cell models that recapitulate human alveolar biology. Here, we apply CRISPR interference to interrogate the function of nine genes implicated in COPD by GWAS in induced pluripotent stem cell–derived type 2 alveolar epithelial cells (iAT2s). We find that multiple genes implicated by GWAS affect iAT2 function, including differentiation potential, maturation, and/or proliferation. Detailed characterization of the GWAS gene DSP demonstrates that it regulates iAT2 cell-cell junctions, proliferation, mitochondrial function, and response to cigarette smoke–induced injury. Our approach thus elucidates the biological function, as well as disease-relevant consequences of dysfunction, of genes implicated in COPD by GWAS in type 2 alveolar epithelial cells.
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