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Effect of Regulator of G Protein Signaling Proteins on Bone

期刊

FRONTIERS IN ENDOCRINOLOGY
卷 13, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2022.842421

关键词

bone homeostasis; osteoclast (OC); osteoblast (OB); chondrocyte; GPCR (G protein coupled receptor); bone development; regulator of G protein signaling (RGS)

资金

  1. National Institute on Aging [NIA] [AG048388]
  2. National Institute of Arthritis and Musculoskeletal and Skin Diseases [NIAMS] [AR066101]
  3. Department of Defense office of the Congressionally Directed Medical Research Programs [CDMRP] [PR201467]
  4. Penn Center for Musculoskeletal Disorders [NIAMS] [P30-AR069619]

向作者/读者索取更多资源

This review summarizes the role of RGS proteins in bone homeostasis and diseases, focusing on their regulation of osteoblasts, chondrocytes, and osteoclasts. The impacts of RGS proteins on bone development and related diseases are highlighted, suggesting their potential as drug targets.
Regulator of G protein signaling (RGS) proteins are critical negative molecules of G protein-coupled receptor (GPCR) signaling, which mediates a variety of biological processes in bone homeostasis and diseases. The RGS proteins are divided into nine subfamilies with a conserved RGS domain which plays an important role in regulating the GTPase activity. Mutations of some RGS proteins change bone development and/or metabolism, causing osteopathy. In this review, we summarize the recent findings of RGS proteins in regulating osteoblasts, chondrocytes, and osteoclasts. We also highlight the impacts of RGS on bone development, bone remodeling, and bone-related diseases. Those studies demonstrate that RGS proteins might be potential drug targets for bone diseases.

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