| Literature DB >> 31042481 |
Yuanyuan Xue1, Denghui Liu2, Guizhong Cui3, Yanyan Ding1, Daosheng Ai4, Suwei Gao5, Yifan Zhang1, Shengbao Suo2, Xiaohan Wang1, Peng Lv1, Chunyu Zhou2, Yizhou Li4, Xingwei Chen2, Guangdun Peng6, Naihe Jing6, Jing-Dong J Han7, Feng Liu8.
Abstract
In vertebrates, hematopoiesis occurring in different niches is orchestrated by intrinsic and extrinsic regulators. Previous studies have revealed numerous linear and planar regulatory mechanisms. However, a multi-dimensional transcriptomic atlas of any given hematopoietic organ has not yet been established. Here, we use multiple RNA sequencing (RNA-seq) approaches, including cell type-specific, temporal bulk RNA-seq, in vivo GEO-seq, and single-cell RNA-seq (scRNA-seq), to characterize the detailed spatiotemporal transcriptome during hematopoietic stem and progenitor cell (HSPC) expansion in the caudal hematopoietic tissue (CHT) of zebrafish. Combinatorial expression profiling reveals that, in the CHT niche, HSPCs and their neighboring supporting cells are co-regulated by shared signaling pathways and intrinsic factors, such as integrin signaling and Smchd1. Moreover, scRNA-seq analysis unveils the strong association between cell cycle status and HSPC differentiation. Taken together, we report a global transcriptome landscape that provides valuable insights and a rich resource to understand HSPC expansion in an intact vertebrate hematopoietic organ.Entities:
Keywords: 3D atlas; hematopoietic stem and progenitor cell; multi-dimensional RNA-seq; signaling; zebrafish
Mesh:
Year: 2019 PMID: 31042481 DOI: 10.1016/j.celrep.2019.04.030
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423