4.7 Article

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

Journal

DEVELOPMENT
Volume 136, Issue 16, Pages 2747-2756

Publisher

COMPANY BIOLOGISTS LTD
DOI: 10.1242/dev.033571

Keywords

Gpr48 (Lgr4); Atf4; Bone formation; Bone remodeling; Mouse

Funding

  1. Science and Technology Commission of Shanghai Municipality [06DZ22923]
  2. National Natural Science Foundation of China [30800653]
  3. National Institutes of Health [1R01CA106479]

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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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