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

Cell Rep. 2018 Jul 17;24(3):766-780. doi: 10.1016/j.celrep.2018.06.057.

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.

Keywords: hematopoiesis; hematopoietic stem cells; retinoic acid; single-cell RNA-sequencing; transcriptional heterogeneity.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Compartmentation*
  • Cell Cycle / drug effects
  • Cell Cycle / genetics*
  • Gene Expression Regulation / drug effects
  • Genes, Reporter
  • Genome
  • Hematopoiesis / drug effects
  • Hematopoiesis / genetics
  • Hematopoietic Stem Cell Transplantation
  • Hematopoietic Stem Cells / cytology*
  • Hematopoietic Stem Cells / drug effects
  • Hematopoietic Stem Cells / metabolism*
  • Luminescent Proteins / metabolism
  • Mice
  • Signal Transduction / drug effects
  • Transcription, Genetic* / drug effects
  • Transcriptome / genetics
  • Tretinoin / pharmacology

Substances

  • Luminescent Proteins
  • Tretinoin