Literature DB >> 19605502

Regulation of bone formation and remodeling by G-protein-coupled receptor 48.

Jian Luo1, Wei Zhou, Xin Zhou, Dali Li, Jinsheng Weng, Zhengfang Yi, Sung Gook Cho, Chenghai Li, Tingfang Yi, Xiushan Wu, Xiao-Ying Li, Benoit de Crombrugghe, Magnus Höök, Mingyao Liu.   

Abstract

G-protein-coupled receptor (GPCR) 48 (Gpr48; Lgr4), a newly discovered member of the glycoprotein hormone receptor subfamily of GPCRs, is an orphan GPCR of unknown function. Using a knockout mouse model, we have characterized the essential roles of Gpr48 in bone formation and remodeling. Deletion of Gpr48 in mice results in a dramatic delay in osteoblast differentiation and mineralization, but not in chondrocyte proliferation and maturation, during embryonic bone formation. Postnatal bone remodeling is also significantly affected in Gpr48(-/-) mice, including the kinetic indices of bone formation rate, bone mineral density and osteoid formation, whereas the activity and number of osteoclasts are increased as assessed by tartrate-resistant acid phosphatase staining. Examination of the molecular mechanism of Gpr48 action in bone formation revealed that Gpr48 can activate the cAMP-PKA-CREB signaling pathway to regulate the expression level of Atf4 in osteoblasts. Furthermore, we show that Gpr48 significantly downregulates the expression levels of Atf4 target genes/proteins, such as osteocalcin (Ocn; Bglap2), bone sialoprotein (Bsp; Ibsp) and collagen. Together, our data demonstrate that Gpr48 regulates bone formation and remodeling through the cAMP-PKA-Atf4 signaling pathway.

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Year:  2009        PMID: 19605502      PMCID: PMC2730404          DOI: 10.1242/dev.033571

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  42 in total

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  66 in total

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3.  Lgr4 protein deficiency induces ataxia-like phenotype in mice and impairs long term depression at cerebellar parallel fiber-Purkinje cell synapses.

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7.  Lgr4/Gpr48 negatively regulates TLR2/4-associated pattern recognition and innate immunity by targeting CD14 expression.

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