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Local Bone Marrow Renin-Angiotensin System and Atherosclerosis

Local hematopoietic bone marrow (BM) renin-angiotensin system (RAS) affects the growth, production, proliferation differentiation, and function of hematopoietic cells. Angiotensin II (Ang II), the dominant effector peptide of the RAS, regulates cellular growth in a wide variety of tissues in pathobi...

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Autores principales: Beyazit, Yavuz, Purnak, Tugrul, Guven, Gulay Sain, Haznedaroglu, Ibrahim C.
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014698/
https://www.ncbi.nlm.nih.gov/pubmed/21234405
http://dx.doi.org/10.4061/2011/714515
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author Beyazit, Yavuz
Purnak, Tugrul
Guven, Gulay Sain
Haznedaroglu, Ibrahim C.
author_facet Beyazit, Yavuz
Purnak, Tugrul
Guven, Gulay Sain
Haznedaroglu, Ibrahim C.
author_sort Beyazit, Yavuz
collection PubMed
description Local hematopoietic bone marrow (BM) renin-angiotensin system (RAS) affects the growth, production, proliferation differentiation, and function of hematopoietic cells. Angiotensin II (Ang II), the dominant effector peptide of the RAS, regulates cellular growth in a wide variety of tissues in pathobiological states. RAS, especially Ang II and Ang II type 1 receptor (AT1R), has considerable proinflammatory and proatherogenic effects on the vessel wall, causing progression of atherosclerosis. Recent investigations, by analyzing several BM chimeric mice whose BM cells were positive or negative for AT1R, disclosed that AT1R in BM cells participates in the pathogenesis of atherosclerosis. Therefore, AT1R blocking not only in vascular cells but also in the BM could be an important therapeutic approach to prevent atherosclerosis. The aim of this paper is to review the function of local BM RAS in the pathogenesis of atherosclerosis.
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spelling pubmed-30146982011-01-13 Local Bone Marrow Renin-Angiotensin System and Atherosclerosis Beyazit, Yavuz Purnak, Tugrul Guven, Gulay Sain Haznedaroglu, Ibrahim C. Cardiol Res Pract Review Article Local hematopoietic bone marrow (BM) renin-angiotensin system (RAS) affects the growth, production, proliferation differentiation, and function of hematopoietic cells. Angiotensin II (Ang II), the dominant effector peptide of the RAS, regulates cellular growth in a wide variety of tissues in pathobiological states. RAS, especially Ang II and Ang II type 1 receptor (AT1R), has considerable proinflammatory and proatherogenic effects on the vessel wall, causing progression of atherosclerosis. Recent investigations, by analyzing several BM chimeric mice whose BM cells were positive or negative for AT1R, disclosed that AT1R in BM cells participates in the pathogenesis of atherosclerosis. Therefore, AT1R blocking not only in vascular cells but also in the BM could be an important therapeutic approach to prevent atherosclerosis. The aim of this paper is to review the function of local BM RAS in the pathogenesis of atherosclerosis. SAGE-Hindawi Access to Research 2010-12-22 /pmc/articles/PMC3014698/ /pubmed/21234405 http://dx.doi.org/10.4061/2011/714515 Text en Copyright © 2011 Yavuz Beyazit et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Beyazit, Yavuz
Purnak, Tugrul
Guven, Gulay Sain
Haznedaroglu, Ibrahim C.
Local Bone Marrow Renin-Angiotensin System and Atherosclerosis
title Local Bone Marrow Renin-Angiotensin System and Atherosclerosis
title_full Local Bone Marrow Renin-Angiotensin System and Atherosclerosis
title_fullStr Local Bone Marrow Renin-Angiotensin System and Atherosclerosis
title_full_unstemmed Local Bone Marrow Renin-Angiotensin System and Atherosclerosis
title_short Local Bone Marrow Renin-Angiotensin System and Atherosclerosis
title_sort local bone marrow renin-angiotensin system and atherosclerosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3014698/
https://www.ncbi.nlm.nih.gov/pubmed/21234405
http://dx.doi.org/10.4061/2011/714515
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