Differences in Cell Cycle Status Underlie Transcriptional Heterogeneity in the HSC Compartment.

Cell Rep

The Finsen Laboratory, Rigshospitalet, Faculty of Health Sciences, University of Copenhagen, 2200 Copenhagen, Denmark; Biotech Research and Innovation Center (BRIC), University of Copenhagen, 2200 Copenhagen, Denmark; Novo Nordisk Foundation Center for Stem Cell Biology, DanStem, Faculty of Health Sciences, University of Copenhagen, 2200 Copenhagen, Denmark. Electronic address:

Published: July 2018

AI Article Synopsis

  • * Gene expression analysis indicated that RA-CFP-dim HSCs had higher levels of RA-target genes, although both subtypes reacted similarly to RA stimuli in lab tests.
  • * Advanced techniques like single-cell RNA sequencing highlighted that variations in cell cycle activity are key to the differences seen in HSCs, revealing that these cells often display low-level expressions of genes related to different lineages

Article 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.

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Source
http://dx.doi.org/10.1016/j.celrep.2018.06.057DOI Listing

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