计算生物学
生物
清脆的
血管疾病
染色质
细胞
血管组织
电池类型
转录因子
血管平滑肌
核糖核酸
神经科学
细胞生物学
功能(生物学)
转录组
生物信息学
血管生成
基因组学
内皮干细胞
Cas9
细胞功能
基因组编辑
疾病
抄写(语言学)
血管畸形
作者
William Schwartzman,Jiahao Jiang,Jathin S. Rao,Gavin R. Schnitzler,Mohita Maurya,Lily Widdup,Mark E. Pepin,Helen Kang,Cindy X. Zheng,Rajat M. Gupta
出处
期刊:Circulation Research
[Lippincott Williams & Wilkins]
日期:2026-01-02
卷期号:138 (1): e326001-e326001
被引量:3
标识
DOI:10.1161/circresaha.125.326001
摘要
Almost 200 years of histological and molecular analysis has established that functional shifts in vascular cell populations are associated with healthy vascular function and the progression of vascular disease. Now, new methods in single-cell analysis are serving to dramatically accelerate the study of vascular cell heterogeneity. Here, we will outline the experimental and computational technologies that have made high-throughput analysis of single cells possible, and review recent studies applying these approaches to vascular cells and tissues. In particular, the application of single-cell or single-nucleus RNA sequencing has identified rare and disease-specific cell populations, drivers of cellular heterogeneity, and specific vascular disease-relevant cell populations. High-throughput approaches linking CRISPR (clustered regularly interspaced short palindromic repeats) perturbations to single-cell RNA sequencing data are providing new insights into cell type-specific mechanisms of disease, and connecting human genetic data to these mechanisms. Other single-cell approaches are providing insights into regulatory mechanisms by linking chromatin accessibility to transcription in single cells and revealing the spatial positioning of rare cell types in vascular tissues. With a variety of well-established methods and the continued development of new technologies, single-cell approaches are becoming indispensable and powerful avenues for discovering and detailing new mechanisms of vascular disease.
科研通智能强力驱动
Strongly Powered by AbleSci AI