Heterotypic interaction promotes asymmetric division of human hematopoietic progenitors

Author:

Candelas Adrian1ORCID,Vianay Benoit2ORCID,Gelin Matthieu1ORCID,Faivre Lionel3,Larghero Jerome3,Blanchoin Laurent2ORCID,Théry Manuel12ORCID,Brunet Stéphane1ORCID

Affiliation:

1. INSERM Unit 976, Institut de Recherche St Louis, AP-HP, Hôpital Saint-Louis, Université Paris Cité 1 Human Immunology, Pathophysiology, Immunotherapy , , F-75010 Paris , France

2. Cytomorpholab, University Grenoble-Alpes, CEA, CNRS, INRA, Laboratoire de Phyiologie Cellulaire & Végétale 2 , F-38054 Grenoble , France

3. INSERM Unit 976, AP-HP, Hôpital Saint-Louis, Center of Clinical Investigations in Biotherapies of Cancer CBT501, Université Paris Cité 3 Unité de Thérapie Cellulaire, Human Immunology, Pathophysiology, Immunotherapy , , F-75010 Paris , France

Abstract

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.

Funder

European Research Council

Fondation Bettencourt Schueller

Fondation Schlumberger pour l'Education et la Recherche

Fondation pour la Recherche Médicale

Publisher

The Company of Biologists

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