Role of CDMP-1 in skeletal morphogenesis: Promotion of mesenchymal cell recruitment and chondrocyte differentiation

被引:145
作者
Tsumaki, N
Tanaka, K
Arikawa-Hirasawa, E
Nakase, T
Kimura, T
Thomas, JT
Ochi, T
Luyten, FP
Yamada, Y
机构
[1] Natl Inst Dent & Craniofacial Res, Craniofacial Dev Biol & Regenerat Branch, NIH, Bethesda, MD 20892 USA
[2] Natl Inst Dent & Craniofacial Res, Craniofacial & Skeletal Dis Branch, NIH, Bethesda, MD 20892 USA
[3] Osaka Univ, Sch Med, Dept Orthopaed Surg, Suita, Osaka 5650871, Japan
[4] Toyama Med & Pharmaceut Univ, Dept Orthopaed Surg, Toyama 9300194, Japan
关键词
bone morphogenetic protein family; cartilage; ectopic expression; skeletal abnormalities; transgenic mice;
D O I
10.1083/jcb.144.1.161
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Cartilage provides the template for endochondral ossification and is crucial for determining the length and width of the skeleton. Transgenic mice with targeted expression of recombinant cartilage-derived morphogenetic protein-1 (CDMP-1), a member of the bone morphogenetic protein family, were created to investigate the role of CDMP-1 in skeletal formation. The mice exhibited chondrodysplasia with expanded cartilage, which consists of the enlarged hypertrophic zone and the reduced proliferating chondrocyte zone. Histologically, CDMP-1 increased the number of chondroprogenitor cells and accelerated chondrocyte differentiation to hypertrophy. Expression of CDMP-1 in the notochord inhibited vertebral body formation by blocking migration of sclerotome cells to the notochord. These results indicate that CDMP-1 antagonizes the ventralization signals from the notochord. Our study suggests a molecular mechanism by which CDMP-1 regulates the formation, growth, and differentiation of the skeletal elements.
引用
收藏
页码:161 / 173
页数:13
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