Phenotypic and proteomic characterization of the human erythroid progenitor continuum reveal dynamic changes in cell cycle and in metabolic pathways

• Published in: American journal of hematology 2024-01, Vol.99 (1), p.99-112
• Main Authors: Papoin, Julien, Yan, Hongxia, Leduc, Marjorie, Le Gall, Morgane, Narla, Anupama, Palis, James, Steiner, Laurie A., Gallagher, Patrick G., Hillyer, Christopher D., Gautier, Emilie‐Fleur, Mohandas, Narla, Blanc, Lionel
• Format: Article
• Language: English
• Subjects: Cell Cycle; Cell Differentiation; Erythrocytes; Erythroid Precursor Cells; Erythropoiesis; Glycolysis; Growth factors; Hematology; Hematopoietic Stem Cells; Humans; Intercellular Signaling Peptides and Proteins - metabolism; Life Sciences; Mass spectroscopy; Metabolic Networks and Pathways; Metabolic pathways; Oxidative phosphorylation; Phosphorylation; Progenitor cells; Proteomes; Proteomics
• ISSN: 0361-8609; 1096-8652; 1096-8652
• DOI: 10.1002/ajh.27145

Human erythropoiesis is a complex process leading to the production of 2.5 million red blood cells per second. Following commitment of hematopoietic stem cells to the erythroid lineage, this process can be divided into three distinct stages: erythroid progenitor differentiation, terminal erythropoiesis, and reticulocyte maturation. We recently resolved the heterogeneity of erythroid progenitors into four different subpopulations termed EP1–EP4. Here, we characterized the growth factor(s) responsiveness of these four progenitor populations in terms of proliferation and differentiation. Using mass spectrometry‐based proteomics on sorted erythroid progenitors, we quantified the absolute expression of ~5500 proteins from EP1 to EP4. Further functional analyses highlighted dynamic changes in cell cycle in these populations with an acceleration of the cell cycle during erythroid progenitor differentiation. The finding that E2F4 expression was increased from EP1 to EP4 is consistent with the noted changes in cell cycle. Finally, our proteomic data suggest that the protein machinery necessary for both oxidative phosphorylation and glycolysis is present in these progenitor cells. Together, our data provide comprehensive insights into growth factor‐dependence of erythroid progenitor proliferation and the proteome of four distinct populations of human erythroid progenitors which will be a useful framework for the study of erythroid disorders. In this study, Papoin, Yan et al. study human erythroid progenitors' response to growth factors and provide a comprehensive characterization of their proteome.