| Literature DB >> 30021172 |
Felicia Kathrine Bratt Lauridsen1, Tanja Lyholm Jensen1, Nicolas Rapin1, Derya Aslan1, Anna Sofia Wilhelmson1, Sachin Pundhir1, Matilda Rehn1, Franziska Paul2, Amir Giladi2, Marie Sigurd Hasemann1, Palle Serup3, Ido Amit2, Bo Torben Porse4.
Abstract
Hematopoietic stem cells (HSCs) are considered a heterogeneous cell population. To further resolve the HSC compartment, we characterized a retinoic acid (RA) reporter mouse line. Sub-fractionation of the HSC compartment in RA-CFP reporter mice demonstrated that RA-CFP-dim HSCs were largely non-proliferative and displayed superior engraftment potential in comparison with RA-CFP-bright HSCs. Gene expression analysis demonstrated higher expression of RA-target genes in RA-CFP-dim HSCs, in contrast to the RA-CFP reporter expression, but both RA-CFP-dim and RA-CFP-bright HSCs responded efficiently to RA in vitro. Single-cell RNA sequencing (RNA-seq) of >1,200 HSCs showed that differences in cell cycle activity constituted the main driver of transcriptional heterogeneity in HSCs. Moreover, further analysis of the single-cell RNA-seq data revealed that stochastic low-level expression of distinct lineage-affiliated transcriptional programs is a common feature of HSCs. Collectively, this work demonstrates the utility of the RA-CFP reporter line as a tool for the isolation of superior HSCs.Entities:
Keywords: hematopoiesis; hematopoietic stem cells; retinoic acid; single-cell RNA-sequencing; transcriptional heterogeneity
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Year: 2018 PMID: 30021172 DOI: 10.1016/j.celrep.2018.06.057
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423