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Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin

Skeleton was considered as a dynamic connective tissue, which was essential for mobility, calcium homeostasis, and hematopoietic niche. However more and more evidences indicate that skeleton works not only as a structural scaffold but also as an endocrine organ, which regulates several metabolic pro...

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Detalles Bibliográficos
Autores principales: Shao, Jin, Wang, Zhi, Yang, Tieyi, Ying, Hui, Zhang, Yan, Liu, Shuyi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383405/
https://www.ncbi.nlm.nih.gov/pubmed/25873961
http://dx.doi.org/10.1155/2015/967673
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author Shao, Jin
Wang, Zhi
Yang, Tieyi
Ying, Hui
Zhang, Yan
Liu, Shuyi
author_facet Shao, Jin
Wang, Zhi
Yang, Tieyi
Ying, Hui
Zhang, Yan
Liu, Shuyi
author_sort Shao, Jin
collection PubMed
description Skeleton was considered as a dynamic connective tissue, which was essential for mobility, calcium homeostasis, and hematopoietic niche. However more and more evidences indicate that skeleton works not only as a structural scaffold but also as an endocrine organ, which regulates several metabolic processes. Besides osteoprotegerin (OPG), sclerostin (SOST), and Dickopf (DKK) which play essential roles in bone formation, modelling, remodelling, and homeostasis, bone can also secret hormones, such as osteocalcin (OCN), which promotes proliferation of β cells, insulin secretion, and insulin sensitivity. Additionally OCN can also regulate the fat cells and male gonad endocrine activity and be regulated by insulin and the neural system. In summary, skeleton has endocrine function via OCN and plays an important role in energy metabolism, especially in glucose metabolism.
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spelling pubmed-43834052015-04-13 Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin Shao, Jin Wang, Zhi Yang, Tieyi Ying, Hui Zhang, Yan Liu, Shuyi Int J Endocrinol Review Article Skeleton was considered as a dynamic connective tissue, which was essential for mobility, calcium homeostasis, and hematopoietic niche. However more and more evidences indicate that skeleton works not only as a structural scaffold but also as an endocrine organ, which regulates several metabolic processes. Besides osteoprotegerin (OPG), sclerostin (SOST), and Dickopf (DKK) which play essential roles in bone formation, modelling, remodelling, and homeostasis, bone can also secret hormones, such as osteocalcin (OCN), which promotes proliferation of β cells, insulin secretion, and insulin sensitivity. Additionally OCN can also regulate the fat cells and male gonad endocrine activity and be regulated by insulin and the neural system. In summary, skeleton has endocrine function via OCN and plays an important role in energy metabolism, especially in glucose metabolism. Hindawi Publishing Corporation 2015 2015-03-19 /pmc/articles/PMC4383405/ /pubmed/25873961 http://dx.doi.org/10.1155/2015/967673 Text en Copyright © 2015 Jin Shao et al. https://creativecommons.org/licenses/by/3.0/ 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
Shao, Jin
Wang, Zhi
Yang, Tieyi
Ying, Hui
Zhang, Yan
Liu, Shuyi
Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin
title Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin
title_full Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin
title_fullStr Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin
title_full_unstemmed Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin
title_short Bone Regulates Glucose Metabolism as an Endocrine Organ through Osteocalcin
title_sort bone regulates glucose metabolism as an endocrine organ through osteocalcin
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4383405/
https://www.ncbi.nlm.nih.gov/pubmed/25873961
http://dx.doi.org/10.1155/2015/967673
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