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

被引:154
作者
Luo, Jian [1 ,2 ,3 ,5 ]
Zhou, Wei [3 ]
Zhou, Xin [4 ]
Li, Dali [1 ,2 ,3 ]
Weng, Jinsheng [3 ]
Yi, Zhengfang [1 ,2 ]
Cho, Sung Gook [3 ]
Li, Chenghai [1 ,2 ]
Yi, Tingfang [3 ]
Wu, Xiushan [5 ]
Li, Xiao-Ying [6 ]
de Crombrugghe, Benoit [4 ]
Hoeoek, Magnus [3 ]
Liu, Mingyao [1 ,2 ,3 ]
机构
[1] E China Normal Univ, Inst Biomed Sci, Shanghai 200241, Peoples R China
[2] E China Normal Univ, Sch Life Sci, Shanghai 200241, Peoples R China
[3] Texas A&M Univ Syst Hlth Sci Ctr, Alkek Inst Biosci & Technol, Houston, TX 77030 USA
[4] Univ Texas MD Anderson Canc Ctr, Houston, TX 77030 USA
[5] Hunan Normal Univ, Coll Life Sci, Changsha 410081, Hunan, Peoples R China
[6] Shanghai Jiao Tong Univ, Rui Jin Hosp, Sch Med, Shanghai Inst Endocrinol & Metab, Shanghai 200025, Peoples R China
来源
DEVELOPMENT | 2009年 / 136卷 / 16期
基金
中国国家自然科学基金; 美国国家卫生研究院;
关键词
Gpr48 (Lgr4); Atf4; Bone formation; Bone remodeling; Mouse; ACTIVATING TRANSCRIPTION FACTOR-4; PARATHYROID-HORMONE; DOWN-REGULATION; GENE; EXPRESSION; LGR4; MECHANISMS; RESORPTION; GPR48; CELLS;
D O I
10.1242/dev.033571
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
引用
收藏
页码:2747 / 2756
页数:10
相关论文
共 42 条
[1]   Interactions between Sox9 and β-catenin control chondrocyte differentiation [J].
Akiyama, H ;
Lyons, JP ;
Mori-Akiyama, Y ;
Yang, XH ;
Zhang, R ;
Zhang, ZP ;
Deng, JM ;
Taketo, MM ;
Nakamura, T ;
Behringer, RR ;
McCrea, PD ;
de Crombrugghe, B .
GENES & DEVELOPMENT, 2004, 18 (09) :1072-1087
[2]   Bone remodeling after renal transplantation [J].
Bellorin-Font, E ;
Rojas, E ;
Carlini, RG ;
Suniaga, O ;
Weisinger, JR .
KIDNEY INTERNATIONAL, 2003, 63 :S125-S128
[3]   OSTEOCALCIN GENE PROMOTER-BINDING FACTORS ARE TISSUE-SPECIFIC NUCLEAR MATRIX COMPONENTS [J].
BIDWELL, JP ;
VANWIJNEN, AJ ;
FEY, EG ;
DWORETZKY, S ;
PENMAN, S ;
STEIN, JL ;
LIAN, JB ;
STEIN, GS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (08) :3162-3166
[4]  
Cancedda R, 2000, INT J DEV BIOL, V44, P707
[5]   SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation [J].
Dobreva, Gergana ;
Chahrour, Maria ;
Dautzenberg, Marcel ;
Chirivella, Laura ;
Kanzler, Benoit ;
Farinas, Isabel ;
Karsenty, Gerard ;
Grosschedl, Rudolf .
CELL, 2006, 125 (05) :971-986
[6]  
DUCY P, 1995, MOL CELL BIOL, V15, P1858
[7]   Leptin regulation of bone resorption by the sympathetic nervous system and CART [J].
Elefteriou, F ;
Ahn, JD ;
Takeda, S ;
Starbuck, M ;
Yang, XL ;
Liu, XY ;
Kondo, H ;
Richards, WG ;
Bannon, TW ;
Noda, M ;
Clement, K ;
Vaisse, C ;
Karsenty, G .
NATURE, 2005, 434 (7032) :514-520
[8]   Bone formation: The nuclear matrix reloaded [J].
Ellies, Debra L. ;
Krumlauf, Robb .
CELL, 2006, 125 (05) :840-842
[9]   TOWARD A MOLECULAR UNDERSTANDING OF SKELETAL DEVELOPMENT [J].
ERLEBACHER, A ;
FILVAROFF, EH ;
GITELMAN, SE ;
DERYNCK, R .
CELL, 1995, 80 (03) :371-378
[10]   The PERK/elF2α/ATF4 module of the UPR in hypoxia resistance and tumor growth [J].
Fels, Diane R. ;
Koumenis, Constantinos .
CANCER BIOLOGY & THERAPY, 2006, 5 (07) :723-728