Literature DB >> 26123302

Role of Regulators of G Protein Signaling Proteins in Bone Physiology and Pathophysiology.

Joel Jules1, Shuying Yang2, Wei Chen1, Yi-Ping Li3.   

Abstract

Regulators of G protein signaling (RGS) proteins enhance the intrinsic GTPase activity of α subunits of the heterotrimeric G protein complex of G protein-coupled receptors (GPCRs) and thereby inactivate signal transduction initiated by GPCRs. The RGS family consists of nearly 37 members with a conserved RGS homology domain which is critical for their GTPase accelerating activity. RGS proteins are expressed in most tissues, including heart, lung, brain, kidney, and bone and play essential roles in many physiological and pathological processes. In skeletal development and bone homeostasis as well as in many bone disorders, RGS proteins control the functions of various GPCRs, including the parathyroid hormone receptor type 1 and calcium-sensing receptor and also regulate various critical signaling pathways, such as Wnt and calcium oscillations. This chapter will discuss the current findings on the roles of RGS proteins in regulating signaling of key GPCRs in skeletal development and bone homeostasis. We also will examine the current updates of RGS proteins' regulation of calcium oscillations in bone physiology and highlight the roles of RGS proteins in selected bone pathological disorders. Despite the recent advances in bone and mineral research, RGS proteins remain understudied in the skeletal system. Further understanding of the roles of RGS proteins in bone should not only provide great insights into the molecular basis of various bone diseases but also generate great therapeutic drug targets for many bone diseases.
© 2015 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Bone; Bone homeostasis; G protein-coupled receptors; G proteins; Osteoblasts; Osteoclasts; PTH/PTHrP; Regulators of G protein signaling; Skeletal disorders; Wnt

Mesh:

Substances:

Year:  2015        PMID: 26123302      PMCID: PMC4817727          DOI: 10.1016/bs.pmbts.2015.02.002

Source DB:  PubMed          Journal:  Prog Mol Biol Transl Sci        ISSN: 1877-1173            Impact factor:   3.622


  130 in total

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