Single-Cell Transcriptome Analysis Maps the Developmental Track of the Human Heart
Author(s) -
Yueli Cui,
Yuxuan Zheng,
Xixi Liu,
Liying Yan,
Xiaoying Fan,
Jun Yong,
Yuqiong Hu,
Ji Dong,
Qingqing Li,
Xinglong Wu,
Shuai Gao,
Jingyun Li,
Lu Wen,
Jie Qiao,
Fuchou Tang
Publication year - 2019
Publication title -
cell reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.264
H-Index - 154
eISSN - 2639-1856
pISSN - 2211-1247
DOI - 10.1016/j.celrep.2019.01.079
Subject(s) - heart development , transcriptome , biology , gene expression , microbiology and biotechnology , human heart , regeneration (biology) , cell type , gene expression profiling , cell , gene , computational biology , embryonic stem cell , genetics , medicine
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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