Luo Jian, Zhou Wei, Zhou Xin, Li Dali, Weng Jinsheng, Yi Zhengfang, Cho Sung Gook, Li Chenghai, Yi Tingfang, Wu Xiushan, Li Xiao-Ying, de Crombrugghe Benoit, Höök Magnus, Liu Mingyao
The Institute of Biomedical Sciences and School of Life Sciences, East China Normal University, Shanghai, China.
Development. 2009 Aug;136(16):2747-56. doi: 10.1242/dev.033571. Epub 2009 Jul 15.
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.
G蛋白偶联受体(GPCR)48(Gpr48;Lgr4)是GPCRs糖蛋白激素受体亚家族新发现的成员,是一种功能未知的孤儿GPCR。利用基因敲除小鼠模型,我们已明确了Gpr48在骨骼形成和重塑中的重要作用。在胚胎期骨骼形成过程中,小鼠体内Gpr48的缺失导致成骨细胞分化和矿化显著延迟,但软骨细胞增殖和成熟未受影响。Gpr48基因敲除(Gpr48-/-)小鼠的出生后骨骼重塑也受到显著影响,包括骨形成率、骨矿物质密度和类骨质形成的动力学指标,而通过抗酒石酸酸性磷酸酶染色评估发现破骨细胞活性和数量增加。对Gpr48在骨骼形成中作用的分子机制研究表明,Gpr48可激活cAMP-PKA-CREB信号通路,以调节成骨细胞中Atf4的表达水平。此外,我们发现Gpr48可显著下调Atf4靶基因/蛋白如骨钙素(Ocn;Bglap2)、骨唾液蛋白(Bsp;Ibsp)和胶原蛋白的表达水平。总之,我们的数据表明Gpr48通过cAMP-PKA-Atf4信号通路调节骨骼形成和重塑。