纤维化
计算生物学
转录组
生物
基因组学
发病机制
病理
医学
基因组
基因
遗传学
免疫学
基因表达
作者
Prasad Palani Velu,Roxanna E. Abhari,Neil C. Henderson
标识
DOI:10.1126/scitranslmed.adm6783
摘要
Organ fibrosis causes major morbidity and mortality worldwide. Treatments for fibrosis are limited, with organ transplantation being the only cure. Here, we review how various state-of-the-art spatial genomics approaches are being deployed to interrogate fibrosis across multiple organs, providing exciting insights into fibrotic disease pathogenesis. These include the detailed topographical annotation of pathogenic cell populations and states, detection of transcriptomic perturbations in morphologically normal tissue, characterization of fibrotic and homeostatic niches and their cellular constituents, and in situ interrogation of ligand-receptor interactions within these microenvironments. Together, these powerful readouts enable detailed analysis of fibrosis evolution across time and space.
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