Roles of DMP1 Processing in Osteogenesis, Dentinogenesis and Chondrogenesis

被引:26
作者
Sun, Yao [1 ,2 ]
Chen, Li [3 ]
Ma, Su [4 ]
Zhou, Jin [5 ]
Zhang, Hua [1 ]
Feng, Jian Q. [1 ]
Qin, Chunlin [1 ]
机构
[1] Baylor Coll Dent, Texas A&M Hlth Sci Ctr, Dept Biomed Sci, Dallas, TX 75246 USA
[2] Harbin Med Coll, Sch Stomatol, Dept Dent Implants, Harbin, Peoples R China
[3] Harbin Med Coll, Sch Stomatol, Dept Endodont, Harbin, Peoples R China
[4] Harbin Med Coll, Sch Stomatol, Dept Periodont, Harbin, Peoples R China
[5] Harbin Med Coll, Affiliated Hosp 1, Dept Hematol, Harbin, Peoples R China
关键词
Dentin matrix protein 1; Proteolytic processing; Osteogenesis; Dentinogenesis; Chondrogenesis; DENTIN MATRIX PROTEIN-1; IN-VIVO; ACIDIC PHOSPHOPROTEIN; DMP1-DEFICIENT MICE; IDENTIFICATION; CARTILAGE; BONE; BIOMINERALIZATION; EXPRESSION; FRAGMENTS;
D O I
10.1159/000324672
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
Dentin matrix protein 1 (DMP1) is an acidic protein that plays critical roles in osteogenesis and dentinogenesis. Protein chemistry studies have demonstrated that DMP1 primarily exists as processed NH(2)- and COOH-terminal fragments in the extracellular matrix of bone and dentin. Our earlier work showed that the substitution of Asp 213 (a residue at a cleavage site) by Ala 213 blocks the processing of mouse DMP1 in vitro. Recently, we generated transgenic mice expressing this mutant DMP1 (designated 'D213A-DMP1'). By crossbreeding these transgenic mice with Dmp1-knockout (Dmp1-KO) mice, we obtained mice expressing the D213A-DMP1 transgene in the Dmp1-null background (named 'Dmp1-KO/D213A-Tg' mice). In this study, we analyzed the long bone, mandible, dentin, and cartilage of Dmp1-KO/D213A-Tg mice in comparison with wild-type, Dmp1-KO, and Dmp1-KO mice expressing the normal DMP1 transgene (Dmp1-KO/normal-Tg). Our results showed that D213A-DMP1 was barely cleaved in the dentin matrix of Dmp1-KO/D213A-Tg mice and the expression of D213A-DMP1 failed to rescue the developmental defects in Dmp1-null mice. Interestingly, enlarged growth plates and condylar cartilages were observed in Dmp1-KO/D213A-Tg mice, indicating a potential role of the full-length form of DMP1 in chondrogenesis. Copyright (C) 2011 S. Karger AG, Basel
引用
收藏
页码:199 / 204
页数:6
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