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A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow

Although the expression of PECAM-1 (CD31) on vascular and haematopoietic cells within the bone marrow microenvironment has been recognized for some time, its physiological role within this niche remains unexplored. In this study we show that PECAM-1 influences steady state hematopoietic stem cell (H...

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Autores principales: Ross, Ewan A., Freeman, Sylvie, Zhao, Yan, Dhanjal, Tarvinder S., Ross, Emma J., Lax, Sian, Ahmed, Zubair, Hou, Tie Zheng, Kalia, Neena, Egginton, Stuart, Nash, Gerard, Watson, Steve P., Frampton, Jon, Buckley, Christopher D.
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394654/
https://www.ncbi.nlm.nih.gov/pubmed/18523558
http://dx.doi.org/10.1371/journal.pone.0002338
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author Ross, Ewan A.
Freeman, Sylvie
Zhao, Yan
Dhanjal, Tarvinder S.
Ross, Emma J.
Lax, Sian
Ahmed, Zubair
Hou, Tie Zheng
Kalia, Neena
Egginton, Stuart
Nash, Gerard
Watson, Steve P.
Frampton, Jon
Buckley, Christopher D.
author_facet Ross, Ewan A.
Freeman, Sylvie
Zhao, Yan
Dhanjal, Tarvinder S.
Ross, Emma J.
Lax, Sian
Ahmed, Zubair
Hou, Tie Zheng
Kalia, Neena
Egginton, Stuart
Nash, Gerard
Watson, Steve P.
Frampton, Jon
Buckley, Christopher D.
author_sort Ross, Ewan A.
collection PubMed
description Although the expression of PECAM-1 (CD31) on vascular and haematopoietic cells within the bone marrow microenvironment has been recognized for some time, its physiological role within this niche remains unexplored. In this study we show that PECAM-1 influences steady state hematopoietic stem cell (HSC) progenitor numbers in the peripheral blood but not the bone marrow compartment. PECAM-1(−/−) mice have higher levels of HSC progenitors in the blood compared to their littermate controls. We show that PECAM-1 is required on both progenitors and bone marrow vascular cells in order for efficient transition between the blood and bone marrow to occur. We have identified key roles for PECAM-1 in both the regulation of HSC migration to the chemokine CXCL12, as well as maintaining levels of the matrix degrading enzyme MMP-9 in the bone marrow vascular niche. Using intravital microscopy and adoptive transfer of either wild type (WT) or PECAM-1(−/−) bone marrow precursors, we demonstrate that the increase in HSC progenitors in the blood is due in part to a reduced ability to migrate from blood to the bone marrow vascular niche. These findings suggest a novel role for PECAM-1 as a regulator of resting homeostatic progenitor cell numbers in the blood
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spelling pubmed-23946542008-06-04 A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow Ross, Ewan A. Freeman, Sylvie Zhao, Yan Dhanjal, Tarvinder S. Ross, Emma J. Lax, Sian Ahmed, Zubair Hou, Tie Zheng Kalia, Neena Egginton, Stuart Nash, Gerard Watson, Steve P. Frampton, Jon Buckley, Christopher D. PLoS One Research Article Although the expression of PECAM-1 (CD31) on vascular and haematopoietic cells within the bone marrow microenvironment has been recognized for some time, its physiological role within this niche remains unexplored. In this study we show that PECAM-1 influences steady state hematopoietic stem cell (HSC) progenitor numbers in the peripheral blood but not the bone marrow compartment. PECAM-1(−/−) mice have higher levels of HSC progenitors in the blood compared to their littermate controls. We show that PECAM-1 is required on both progenitors and bone marrow vascular cells in order for efficient transition between the blood and bone marrow to occur. We have identified key roles for PECAM-1 in both the regulation of HSC migration to the chemokine CXCL12, as well as maintaining levels of the matrix degrading enzyme MMP-9 in the bone marrow vascular niche. Using intravital microscopy and adoptive transfer of either wild type (WT) or PECAM-1(−/−) bone marrow precursors, we demonstrate that the increase in HSC progenitors in the blood is due in part to a reduced ability to migrate from blood to the bone marrow vascular niche. These findings suggest a novel role for PECAM-1 as a regulator of resting homeostatic progenitor cell numbers in the blood Public Library of Science 2008-06-04 /pmc/articles/PMC2394654/ /pubmed/18523558 http://dx.doi.org/10.1371/journal.pone.0002338 Text en Ross 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
Ross, Ewan A.
Freeman, Sylvie
Zhao, Yan
Dhanjal, Tarvinder S.
Ross, Emma J.
Lax, Sian
Ahmed, Zubair
Hou, Tie Zheng
Kalia, Neena
Egginton, Stuart
Nash, Gerard
Watson, Steve P.
Frampton, Jon
Buckley, Christopher D.
A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow
title A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow
title_full A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow
title_fullStr A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow
title_full_unstemmed A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow
title_short A Novel Role for PECAM-1 (CD31) in Regulating Haematopoietic Progenitor Cell Compartmentalization between the Peripheral Blood and Bone Marrow
title_sort novel role for pecam-1 (cd31) in regulating haematopoietic progenitor cell compartmentalization between the peripheral blood and bone marrow
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394654/
https://www.ncbi.nlm.nih.gov/pubmed/18523558
http://dx.doi.org/10.1371/journal.pone.0002338
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