生物
组学
转录组
计算生物学
功能(生物学)
仿形(计算机编程)
干细胞
祖细胞
心血管健康
生物信息学
心血管生理学
现存分类群
心脏发育
追踪
基因组学
电池类型
细胞功能
蛋白质组学
系统生物学
神经科学
祖细胞
数据科学
钥匙(锁)
作者
Rebecca L. Harper,Patrick M. Lelliott,Shawn B. Bender,Alexander R. Pinto
出处
期刊:Circulation Research
[Lippincott Williams & Wilkins]
日期:2026-01-02
卷期号:138 (1): e325793-e325793
被引量:1
标识
DOI:10.1161/circresaha.125.325793
摘要
The cardiovascular system, composed of the heart and vasculature, is essential for blood circulation, nutrient exchange, and waste removal. In the past, our understanding of cardiovascular development and function has largely been shaped by bulk tissue analyses, which obscures cellular heterogeneity. The emergence of single-cell omics has transformed the field by enabling unbiased transcriptional profiling of individual cells, revealing the diversity of stem cells and progenitor cells driving embryogenesis, resulting in the various mature cardiovascular cell types in the adult heart and vasculature. This technology has provided unprecedented insights into the molecular mechanisms governing cardiovascular development and function by identifying novel cell subpopulations, characterizing their unique properties, and tracing their temporal evolution through advanced analytical approaches. In this review, we discuss how single-cell omics has reshaped our understanding of cardiovascular developmental biology, highlight key analytical tools and emerging approaches, examine preclinical models that have facilitated these discoveries, and explore how these technologies have defined the cellular landscape of the heart and vasculature. We conclude by looking ahead to emerging technologies such as spatial transcriptomics and clonal barcoding for lineage tracing, as well as new strategies in addressing the gender gap in cardiovascular research.
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