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Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation

Product of the Itga2b gene, CD41 contributes to hematopoietic stem cell (HSC) and megakaryocyte/platelet functions. CD41 expression marks the onset of definitive hematopoiesis in the embryo where it participates in regulating the numbers of multipotential progenitors. Key to platelet aggregation, CD...

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Autores principales: Dumon, Stephanie, Walton, David S., Volpe, Giacomo, Wilson, Nicola, Dassé, Emilie, Pozzo, Walter Del, Landry, Josette-Renee, Turner, Bryan, O’Neill, Laura P., Göttgens, Berthold, Frampton, Jon
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429474/
https://www.ncbi.nlm.nih.gov/pubmed/22952660
http://dx.doi.org/10.1371/journal.pone.0043300
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author Dumon, Stephanie
Walton, David S.
Volpe, Giacomo
Wilson, Nicola
Dassé, Emilie
Pozzo, Walter Del
Landry, Josette-Renee
Turner, Bryan
O’Neill, Laura P.
Göttgens, Berthold
Frampton, Jon
author_facet Dumon, Stephanie
Walton, David S.
Volpe, Giacomo
Wilson, Nicola
Dassé, Emilie
Pozzo, Walter Del
Landry, Josette-Renee
Turner, Bryan
O’Neill, Laura P.
Göttgens, Berthold
Frampton, Jon
author_sort Dumon, Stephanie
collection PubMed
description Product of the Itga2b gene, CD41 contributes to hematopoietic stem cell (HSC) and megakaryocyte/platelet functions. CD41 expression marks the onset of definitive hematopoiesis in the embryo where it participates in regulating the numbers of multipotential progenitors. Key to platelet aggregation, CD41 expression also characterises their precursor, the megakaryocyte, and is specifically up regulated during megakaryopoiesis. Though phenotypically unique, megakaryocytes and HSC share numerous features, including key transcription factors, which could indicate common sub-regulatory networks. In these respects, Itga2b can serve as a paradigm to study features of both developmental-stage and HSC- versus megakaryocyte-specific regulations. By comparing different cellular contexts, we highlight a mechanism by which internal promoters participate in Itga2b regulation. A developmental process connects epigenetic regulation and promoter switching leading to CD41 expression in HSC. Interestingly, a similar process can be observed at the Mpl locus, which codes for another receptor that defines both HSC and megakaryocyte identities. Our study shows that Itga2b expression is controlled by lineage-specific networks and associates with H4K8ac in megakaryocyte or H3K27me3 in the multipotential hematopoietic cell line HPC7. Correlating with the decrease in H3K27me3 at the Itga2b Iocus, we find that following commitment to megakaryocyte differentiation, the H3K27 demethylase Jmjd3 up-regulation influences both Itga2b and Mpl expression.
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spelling pubmed-34294742012-09-05 Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation Dumon, Stephanie Walton, David S. Volpe, Giacomo Wilson, Nicola Dassé, Emilie Pozzo, Walter Del Landry, Josette-Renee Turner, Bryan O’Neill, Laura P. Göttgens, Berthold Frampton, Jon PLoS One Research Article Product of the Itga2b gene, CD41 contributes to hematopoietic stem cell (HSC) and megakaryocyte/platelet functions. CD41 expression marks the onset of definitive hematopoiesis in the embryo where it participates in regulating the numbers of multipotential progenitors. Key to platelet aggregation, CD41 expression also characterises their precursor, the megakaryocyte, and is specifically up regulated during megakaryopoiesis. Though phenotypically unique, megakaryocytes and HSC share numerous features, including key transcription factors, which could indicate common sub-regulatory networks. In these respects, Itga2b can serve as a paradigm to study features of both developmental-stage and HSC- versus megakaryocyte-specific regulations. By comparing different cellular contexts, we highlight a mechanism by which internal promoters participate in Itga2b regulation. A developmental process connects epigenetic regulation and promoter switching leading to CD41 expression in HSC. Interestingly, a similar process can be observed at the Mpl locus, which codes for another receptor that defines both HSC and megakaryocyte identities. Our study shows that Itga2b expression is controlled by lineage-specific networks and associates with H4K8ac in megakaryocyte or H3K27me3 in the multipotential hematopoietic cell line HPC7. Correlating with the decrease in H3K27me3 at the Itga2b Iocus, we find that following commitment to megakaryocyte differentiation, the H3K27 demethylase Jmjd3 up-regulation influences both Itga2b and Mpl expression. Public Library of Science 2012-08-28 /pmc/articles/PMC3429474/ /pubmed/22952660 http://dx.doi.org/10.1371/journal.pone.0043300 Text en © 2012 Dumon et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Dumon, Stephanie
Walton, David S.
Volpe, Giacomo
Wilson, Nicola
Dassé, Emilie
Pozzo, Walter Del
Landry, Josette-Renee
Turner, Bryan
O’Neill, Laura P.
Göttgens, Berthold
Frampton, Jon
Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation
title Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation
title_full Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation
title_fullStr Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation
title_full_unstemmed Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation
title_short Itga2b Regulation at the Onset of Definitive Hematopoiesis and Commitment to Differentiation
title_sort itga2b regulation at the onset of definitive hematopoiesis and commitment to differentiation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3429474/
https://www.ncbi.nlm.nih.gov/pubmed/22952660
http://dx.doi.org/10.1371/journal.pone.0043300
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