Heterotypic interaction promotes asymmetric division of human hematopoietic progenitors

Development. 2024 Sep 1;151(17):dev203088. doi: 10.1242/dev.203088. Epub 2024 Sep 3.

Abstract

Hematopoietic stem and progenitor cells (HSPCs) give rise to all cell types of the hematopoietic system through various processes, including asymmetric divisions. However, the contribution of stromal cells of the hematopoietic niches in the control of HSPC asymmetric divisions remains unknown. Using polyacrylamide microwells as minimalist niches, we show that specific heterotypic interactions with osteoblast and endothelial cells promote asymmetric divisions of human HSPCs. Upon interaction, HSPCs polarize in interphase with the centrosome, the Golgi apparatus, and lysosomes positioned close to the site of contact. Subsequently, during mitosis, HSPCs orient their spindle perpendicular to the plane of contact. This division mode gives rise to siblings with unequal amounts of lysosomes and of the differentiation marker CD34. Such asymmetric inheritance generates heterogeneity in the progeny, which is likely to contribute to the plasticity of the early steps of hematopoiesis.

Keywords: Asymmetric division; Hematopoiesis; Heterotypic interaction; Human; Microfabrication; Niches; Stem cells.

MeSH terms

  • Antigens, CD34 / metabolism
  • Asymmetric Cell Division
  • Cell Differentiation
  • Cell Division
  • Centrosome / metabolism
  • Endothelial Cells / cytology
  • Endothelial Cells / metabolism
  • Golgi Apparatus / metabolism
  • Hematopoiesis / physiology
  • Hematopoietic Stem Cells* / cytology
  • Hematopoietic Stem Cells* / metabolism
  • Humans
  • Lysosomes / metabolism
  • Mitosis
  • Osteoblasts / cytology
  • Osteoblasts / metabolism

Substances

  • Antigens, CD34