| Literature DB >> 30759401 |
Yueli Cui1, Yuxuan Zheng2, Xixi Liu3, Liying Yan4, Xiaoying Fan1, Jun Yong4, Yuqiong Hu2, Ji Dong1, Qingqing Li1, Xinglong Wu2, Shuai Gao1, Jingyun Li2, Lu Wen1, Jie Qiao5, Fuchou Tang6.
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.Entities:
Keywords: cardiac fibroblasts; cardiomyocytes; cross-species comparison; endothelial cells; extracellular matrix; human embryonic development; human fetal heart development; single-cell RNA-seq; single-cell transcriptome analysis; valvar interstitial cells
Mesh:
Year: 2019 PMID: 30759401 DOI: 10.1016/j.celrep.2019.01.079
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423