转录组
生物
电池类型
人的心脏
心肌细胞
免疫系统
神经科学
心肌
细胞生物学
医学
心室
心脏病
基因表达
内科学
细胞
病理
解剖
基因
免疫学
遗传学
心室
作者
Monika Litviňuková,Carlos Talavera‐López,Henrike Maatz,Daniel Reichart,Catherine L. Worth,Eric L. Lindberg,Masatoshi Kanda,Krzysztof Polański,Matthias Heinig,Michael Lee,Emily R. Nadelmann,Kenny Roberts,Elizabeth Tuck,Eirini S. Fasouli,Daniel M. DeLaughter,Barbara McDonough,Hiroko Wakimoto,Joshua Gorham,Sara Samari,Krishnaa T. Mahbubani
出处
期刊:Nature
[Springer Nature]
日期:2020-09-24
卷期号:588 (7838): 466-472
被引量:1577
标识
DOI:10.1038/s41586-020-2797-4
摘要
Abstract Cardiovascular disease is the leading cause of death worldwide. Advanced insights into disease mechanisms and therapeutic strategies require a deeper understanding of the molecular processes involved in the healthy heart. Knowledge of the full repertoire of cardiac cells and their gene expression profiles is a fundamental first step in this endeavour. Here, using state-of-the-art analyses of large-scale single-cell and single-nucleus transcriptomes, we characterize six anatomical adult heart regions. Our results highlight the cellular heterogeneity of cardiomyocytes, pericytes and fibroblasts, and reveal distinct atrial and ventricular subsets of cells with diverse developmental origins and specialized properties. We define the complexity of the cardiac vasculature and its changes along the arterio-venous axis. In the immune compartment, we identify cardiac-resident macrophages with inflammatory and protective transcriptional signatures. Furthermore, analyses of cell-to-cell interactions highlight different networks of macrophages, fibroblasts and cardiomyocytes between atria and ventricles that are distinct from those of skeletal muscle. Our human cardiac cell atlas improves our understanding of the human heart and provides a valuable reference for future studies.
科研通智能强力驱动
Strongly Powered by AbleSci AI