Integrated molecular analysis identifies a conserved pericyte gene signature in zebrafish

周细胞 生物 PDGFRB公司 斑马鱼 细胞生物学 壁细胞 基因 转录组 报告基因 基因表达 遗传学 内皮干细胞 体外
作者
Yu-Huan Shih,Daneal Portman,Feston Idrizi,Ann S. Grosse,Nathan D. Lawson
出处
期刊:Development [The Company of Biologists]
卷期号:148 (23) 被引量:23
标识
DOI:10.1242/dev.200189
摘要

Pericytes reside in capillary beds where they share a basement membrane with endothelial cells and regulate their function. However, little is known about embryonic pericyte development, in part, due to lack of specific molecular markers and genetic tools. Here, we applied single cell RNA-sequencing (scRNA-seq) of platelet derived growth factor beta (pdgfrb)-positive cells to molecularly characterize pericytes in zebrafish larvae. scRNA-seq revealed zebrafish cells expressing mouse pericyte gene orthologs, and comparison with bulk RNA-seq from wild-type and pdgfrb mutant larvae further refined a pericyte gene set. Subsequent integration with mouse pericyte scRNA-seq profiles revealed a core set of conserved pericyte genes. Using transgenic reporter lines, we validated pericyte expression of two genes identified in our analysis: NDUFA4 mitochondrial complex associated like 2a (ndufa4l2a), and potassium voltage-gated channel, Isk-related family, member 4 (kcne4). Both reporter lines exhibited pericyte expression in multiple anatomical locations, and kcne4 was also detected in a subset of vascular smooth muscle cells. Thus, our integrated molecular analysis revealed a molecular profile for zebrafish pericytes and allowed us to develop new tools to observe these cells in vivo.
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