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Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism

The link between fatty acids and bone metabolism is complex and can be direct and indirect. This link has been reported in different types of bone cells and various stages of bone metabolism. G-protein coupled receptor 120 (GPR120), also called free fatty acid receptor 4 (FFAR4), is a member of the...

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Detalles Bibliográficos
Autores principales: Wang, Yuhan, Liu, Haixia, Zhang, Zhiguo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JKL International LLC 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529742/
https://www.ncbi.nlm.nih.gov/pubmed/37196107
http://dx.doi.org/10.14336/AD.2023.0216
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author Wang, Yuhan
Liu, Haixia
Zhang, Zhiguo
author_facet Wang, Yuhan
Liu, Haixia
Zhang, Zhiguo
author_sort Wang, Yuhan
collection PubMed
description The link between fatty acids and bone metabolism is complex and can be direct and indirect. This link has been reported in different types of bone cells and various stages of bone metabolism. G-protein coupled receptor 120 (GPR120), also called free fatty acid receptor 4 (FFAR4), is a member of the recently discovered G protein-coupled receptor family that can interact with both long-chain saturated fatty acids (C14-C18) and long-chain unsaturated fatty acids (C16-C22). Research shows that GPR120 regulates processes in different types of bone cells, directly or indirectly affecting bone metabolism. Our research reviewed the literature on the effects of GPR120 on bone marrow mesenchymal stem cells (BMMSCs), osteoblasts, osteoclasts, and chondrocytes, focusing on the research findings regarding the mechanism by which GPR120 alters specific bone metabolic diseases-osteoporosis and osteoarthritis. The data reviewed here provide a basis for clinical and basic research into the role of GPR120 on bone metabolic diseases.
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spelling pubmed-105297422023-10-01 Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism Wang, Yuhan Liu, Haixia Zhang, Zhiguo Aging Dis Review The link between fatty acids and bone metabolism is complex and can be direct and indirect. This link has been reported in different types of bone cells and various stages of bone metabolism. G-protein coupled receptor 120 (GPR120), also called free fatty acid receptor 4 (FFAR4), is a member of the recently discovered G protein-coupled receptor family that can interact with both long-chain saturated fatty acids (C14-C18) and long-chain unsaturated fatty acids (C16-C22). Research shows that GPR120 regulates processes in different types of bone cells, directly or indirectly affecting bone metabolism. Our research reviewed the literature on the effects of GPR120 on bone marrow mesenchymal stem cells (BMMSCs), osteoblasts, osteoclasts, and chondrocytes, focusing on the research findings regarding the mechanism by which GPR120 alters specific bone metabolic diseases-osteoporosis and osteoarthritis. The data reviewed here provide a basis for clinical and basic research into the role of GPR120 on bone metabolic diseases. JKL International LLC 2023-10-01 /pmc/articles/PMC10529742/ /pubmed/37196107 http://dx.doi.org/10.14336/AD.2023.0216 Text en copyright: © 2023 Wang et al. https://creativecommons.org/licenses/by/2.0/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 that the original work is properly attributed.
spellingShingle Review
Wang, Yuhan
Liu, Haixia
Zhang, Zhiguo
Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism
title Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism
title_full Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism
title_fullStr Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism
title_full_unstemmed Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism
title_short Recent Advance in Regulatory Effect of GRP120 on Bone Metabolism
title_sort recent advance in regulatory effect of grp120 on bone metabolism
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10529742/
https://www.ncbi.nlm.nih.gov/pubmed/37196107
http://dx.doi.org/10.14336/AD.2023.0216
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