Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones

In addition to its structural role, the skeleton serves as an endocrine organ that controls mineral metabolism and energy homeostasis. Three major cell types in bone - osteoblasts, osteoclasts, and osteocytes – dynamically form and maintain bone and secrete factors with systemic activity. Osteocalci...

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Main Authors: Jialiang S. Wang, Courtney M. Mazur, Marc N. Wein
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-03-01
Series:Frontiers in Endocrinology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2021.584147/full
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author Jialiang S. Wang
Courtney M. Mazur
Marc N. Wein
Marc N. Wein
Marc N. Wein
author_facet Jialiang S. Wang
Courtney M. Mazur
Marc N. Wein
Marc N. Wein
Marc N. Wein
author_sort Jialiang S. Wang
collection DOAJ
description In addition to its structural role, the skeleton serves as an endocrine organ that controls mineral metabolism and energy homeostasis. Three major cell types in bone - osteoblasts, osteoclasts, and osteocytes – dynamically form and maintain bone and secrete factors with systemic activity. Osteocalcin, an osteoblast-derived factor initially described as a matrix protein that regulates bone mineralization, has been suggested to be an osteoblast-derived endocrine hormone that regulates multiple target organs including pancreas, liver, muscle, adipose, testes, and the central and peripheral nervous system. Sclerostin is predominantly produced by osteocytes, and is best known as a paracrine-acting regulator of WNT signaling and activity of osteoblasts and osteoclasts on bone surfaces. In addition to this important paracrine role for sclerostin within bone, sclerostin protein has been noted to act at a distance to regulate adipocytes, energy homeostasis, and mineral metabolism in the kidney. In this article, we aim to bring together evidence supporting an endocrine function for sclerostin and osteocalcin, and discuss recent controversies regarding the proposed role of osteocalcin outside of bone. We summarize the current state of knowledge on animal models and human physiology related to the multiple functions of these bone-derived factors. Finally, we highlight areas in which future research is expected to yield additional insights into the biology of osteocalcin and sclerostin.
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spelling doaj.art-876d1c8ea3bc4f279cd3e6a8e7a0a5852022-12-21T22:55:03ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922021-03-011210.3389/fendo.2021.584147584147Sclerostin and Osteocalcin: Candidate Bone-Produced HormonesJialiang S. Wang0Courtney M. Mazur1Marc N. Wein2Marc N. Wein3Marc N. Wein4Endocrine Unit, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United StatesEndocrine Unit, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United StatesEndocrine Unit, Department of Medicine, Massachusetts General Hospital, Harvard Medical School, Boston, MA, United StatesBroad Institute of Massachusetts Institute of Technology (MIT) and Harvard, Cambridge, MA, United StatesHarvard Stem Cell Institute, Cambridge, MA, United StatesIn addition to its structural role, the skeleton serves as an endocrine organ that controls mineral metabolism and energy homeostasis. Three major cell types in bone - osteoblasts, osteoclasts, and osteocytes – dynamically form and maintain bone and secrete factors with systemic activity. Osteocalcin, an osteoblast-derived factor initially described as a matrix protein that regulates bone mineralization, has been suggested to be an osteoblast-derived endocrine hormone that regulates multiple target organs including pancreas, liver, muscle, adipose, testes, and the central and peripheral nervous system. Sclerostin is predominantly produced by osteocytes, and is best known as a paracrine-acting regulator of WNT signaling and activity of osteoblasts and osteoclasts on bone surfaces. In addition to this important paracrine role for sclerostin within bone, sclerostin protein has been noted to act at a distance to regulate adipocytes, energy homeostasis, and mineral metabolism in the kidney. In this article, we aim to bring together evidence supporting an endocrine function for sclerostin and osteocalcin, and discuss recent controversies regarding the proposed role of osteocalcin outside of bone. We summarize the current state of knowledge on animal models and human physiology related to the multiple functions of these bone-derived factors. Finally, we highlight areas in which future research is expected to yield additional insights into the biology of osteocalcin and sclerostin.https://www.frontiersin.org/articles/10.3389/fendo.2021.584147/fullosteoblastosteocyteosteocalcinsclerostinbone homeostasis
spellingShingle Jialiang S. Wang
Courtney M. Mazur
Marc N. Wein
Marc N. Wein
Marc N. Wein
Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones
Frontiers in Endocrinology
osteoblast
osteocyte
osteocalcin
sclerostin
bone homeostasis
title Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones
title_full Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones
title_fullStr Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones
title_full_unstemmed Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones
title_short Sclerostin and Osteocalcin: Candidate Bone-Produced Hormones
title_sort sclerostin and osteocalcin candidate bone produced hormones
topic osteoblast
osteocyte
osteocalcin
sclerostin
bone homeostasis
url https://www.frontiersin.org/articles/10.3389/fendo.2021.584147/full
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AT courtneymmazur sclerostinandosteocalcincandidateboneproducedhormones
AT marcnwein sclerostinandosteocalcincandidateboneproducedhormones
AT marcnwein sclerostinandosteocalcincandidateboneproducedhormones
AT marcnwein sclerostinandosteocalcincandidateboneproducedhormones