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Competition between hematopoietic stem and progenitor cells controls hematopoietic stem cell compartment size

Author

Listed:
  • Runfeng Miao

    (Yale University School of Medicine)

  • Harim Chun

    (Korea University College of Medicine)

  • Xing Feng

    (Yale University School of Medicine)

  • Ana Cordeiro Gomes

    (Yale University School of Medicine
    i3S – Instituto de Investigação e Inovação em Saúde, University of Porto)

  • Jungmin Choi

    (Korea University College of Medicine
    Yale University School of Medicine)

  • João P. Pereira

    (Yale University School of Medicine)

Abstract

Cellular competition for limiting hematopoietic factors is a physiologically regulated but poorly understood process. Here, we studied this phenomenon by hampering hematopoietic progenitor access to Leptin receptor+ mesenchymal stem/progenitor cells (MSPCs) and endothelial cells (ECs). We show that HSC numbers increase by 2-fold when multipotent and lineage-restricted progenitors fail to respond to CXCL12 produced by MSPCs and ECs. HSCs are qualitatively normal, and HSC expansion only occurs when early hematopoietic progenitors but not differentiated hematopoietic cells lack CXCR4. Furthermore, the MSPC and EC transcriptomic heterogeneity is stable, suggesting that it is impervious to major changes in hematopoietic progenitor interactions. Instead, HSC expansion correlates with increased availability of membrane-bound stem cell factor (mSCF) on MSPCs and ECs presumably due to reduced consumption by cKit-expressing hematopoietic progenitors. These studies suggest that an intricate homeostatic balance between HSCs and proximal hematopoietic progenitors is regulated by cell competition for limited amounts of mSCF.

Suggested Citation

  • Runfeng Miao & Harim Chun & Xing Feng & Ana Cordeiro Gomes & Jungmin Choi & João P. Pereira, 2022. "Competition between hematopoietic stem and progenitor cells controls hematopoietic stem cell compartment size," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-32228-w
    DOI: 10.1038/s41467-022-32228-w
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