Molecular signature of erythroblast enucleation in human embryonic stem cells

Author:

Rouzbeh Shaghayegh123,Kobari Ladan123,Cambot Marie4,Mazurier Christelle1235,Hebert Nicolas1235,Faussat Anne-Marie6,Durand Charles78,Douay Luc12359,Lapillonne Hélène1239

Affiliation:

1. UPMC Univ Paris 06, UMR_S938 CDR Saint-Antoine, Prolifération et Différentiation des Cellules Souches, Paris, France

2. INSERM, UMR_S938, Prolifération et Différentiation des Cellules Souches, Paris, France

3. Laboratory of Excellence GR-Ex, Paris, France

4. Institut National de Transfusion Sanguine INTS, Paris, France

5. EFS Ile de France, Unité d'Ingénierie et de Thérapie Cellulaire, Créteil, France

6. IFR 65-Saint Antoine UMPC, Plateforme de Cytométrie, Paris, France

7. CNRS UMR7622, Laboratoire de biologie et du développement, Paris, France

8. UPMC UMR7622, Laboratoire de biologie et du développement, Paris, France

9. AP-HP, Hôpital St Antoine et Hôpital Trousseau, Service d'Hématologie et Immunologie Biologiques, Paris, France

Abstract

Abstract While enucleation is a critical step in the terminal differentiation of human red blood cells, the molecular mechanisms underlying this unique process remain unclear. To investigate erythroblast enucleation, we studied the erythroid differentiation of human embryonic stem cells (hESCs), which provide a unique model for deeper understanding of the development and differentiation of multiple cell types. First, using a two-step protocol, we demonstrated that terminal erythroid differentiation from hESCs is directly dependent on the age of the embryoid bodies. Second, by choosing hESCs in two extreme conditions of erythroid culture, we obtained an original differentiation model which allows one to study the mechanisms underlying the enucleation of erythroid cells by analyzing the gene and miRNA (miR) expression profiles of cells from these two culture conditions. Third, using an integrated analysis of mRNA and miR expression profiles, we identified five miRs potentially involved in erythroblast enucleation. Finally, by selective knockdown of these five miRs we found miR-30a to be a regulator of erythroblast enucleation in hESCs. Stem Cells  2015;33:2431–2441

Funder

Agence Nationale de la Recherche

Fondation pour la Recherche Médicale

Combattre la Leucémie

DIM Stem Pôle

Etablissement Français du Sang

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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