Single-Cell Transcriptome Analysis Maps the Developmental Track of the Human Heart

Yueli Cui(Peking University), Yuxuan Zheng(Peking University), Xixi Liu(Beijing Obstetrics and Gynecology Hospital), Liying Yan(Beijing Obstetrics and Gynecology Hospital), Xiaoying Fan(Peking University), Jun Yong(Ministry of Education of the People's Republic of China), Yuqiong Hu(Center for Life Sciences), Ji Dong(Peking University), Qingqing Li(Peking University), Xinglong Wu(Peking University), Shuai Gao(Peking University), Jingyun Li(Peking University), Lu Wen(Peking University), Jie Qiao(Center for Life Sciences), Fuchou Tang(Center for Life Sciences)
Cell Reports
February 1, 2019
Cited by 500Open Access
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Abstract

The heart is the central organ of the circulatory system, and its proper development is vital for maintaining human life. Here, we used single-cell RNA sequencing to profile the gene expression landscapes of ∼4,000 cardiac cells from human embryos and identified four major types of cells: cardiomyocytes (CMs), cardiac fibroblasts, endothelial cells (ECs), and valvar interstitial cells (VICs). Atrial and ventricular CMs acquired distinct features early in heart development. Furthermore, both CMs and fibroblasts show stepwise changes in gene expression. As development proceeds, VICs may be involved in the remodeling phase, and ECs display location-specific characteristics. Finally, we compared gene expression profiles between humans and mice and identified a series of unique features of human heart development. Our study lays the groundwork for elucidating the mechanisms of in vivo human cardiac development and provides potential clues to understand cardiac regeneration.


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