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An emerging role for adenosine and its receptors in bone homeostasis

Bone is continually being remodeled and defects in the processes involved lead to bone diseases. Many regulatory factors are known to influence remodeling but other mechanisms, hitherto unknown, may also be involved. Importantly, our understanding of these currently unknown mechanisms may lead to im...

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Detalles Bibliográficos
Autores principales: Ham, Jack, Evans, Bronwen A. J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Research Foundation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444801/
https://www.ncbi.nlm.nih.gov/pubmed/23024635
http://dx.doi.org/10.3389/fendo.2012.00113
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author Ham, Jack
Evans, Bronwen A. J.
author_facet Ham, Jack
Evans, Bronwen A. J.
author_sort Ham, Jack
collection PubMed
description Bone is continually being remodeled and defects in the processes involved lead to bone diseases. Many regulatory factors are known to influence remodeling but other mechanisms, hitherto unknown, may also be involved. Importantly, our understanding of these currently unknown mechanisms may lead to important new therapies for bone disease. It is accepted that purinergic signaling is involved in bone, and our knowledge of this area has increased significantly over the last 15 years, although most of the published work has studied the role of ATP and other signaling molecules via the P2 family of purinergic receptors. During the last few years, however, there has been increased interest within the bone field in the role of P1 receptors where adenosine is the primary signaling molecule. This review will bring together the current information available in relation to this expanding area of research.
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spelling pubmed-34448012012-09-28 An emerging role for adenosine and its receptors in bone homeostasis Ham, Jack Evans, Bronwen A. J. Front Endocrinol (Lausanne) Endocrinology Bone is continually being remodeled and defects in the processes involved lead to bone diseases. Many regulatory factors are known to influence remodeling but other mechanisms, hitherto unknown, may also be involved. Importantly, our understanding of these currently unknown mechanisms may lead to important new therapies for bone disease. It is accepted that purinergic signaling is involved in bone, and our knowledge of this area has increased significantly over the last 15 years, although most of the published work has studied the role of ATP and other signaling molecules via the P2 family of purinergic receptors. During the last few years, however, there has been increased interest within the bone field in the role of P1 receptors where adenosine is the primary signaling molecule. This review will bring together the current information available in relation to this expanding area of research. Frontiers Research Foundation 2012-09-18 /pmc/articles/PMC3444801/ /pubmed/23024635 http://dx.doi.org/10.3389/fendo.2012.00113 Text en Copyright © Ham and Evans. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Endocrinology
Ham, Jack
Evans, Bronwen A. J.
An emerging role for adenosine and its receptors in bone homeostasis
title An emerging role for adenosine and its receptors in bone homeostasis
title_full An emerging role for adenosine and its receptors in bone homeostasis
title_fullStr An emerging role for adenosine and its receptors in bone homeostasis
title_full_unstemmed An emerging role for adenosine and its receptors in bone homeostasis
title_short An emerging role for adenosine and its receptors in bone homeostasis
title_sort emerging role for adenosine and its receptors in bone homeostasis
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3444801/
https://www.ncbi.nlm.nih.gov/pubmed/23024635
http://dx.doi.org/10.3389/fendo.2012.00113
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