PLAP-1/asporin, a novel negative regulator of periodontal ligament mineralization

被引:163
作者
Yamada, Satoru
Tomoeda, Miki
Ozawa, Yasuhiro
Yoneda, Shinya
Terashima, Yoshimitsu
Ikezawa, Kazuhiko
Ikegawa, Shiro
Saito, Masahiro
Toyosawa, Satoru
Murakami, Shinya
机构
[1] Osaka Univ, Grad Sch Dent, Dept Periodontol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Grad Sch Dent, Dept Oral Pathol, Suita, Osaka 5650871, Japan
[3] RIKEN, Single Nucleotide Polymorphisms Res Ctr, Lab Bone & Joint Dis, Minato Ku, Tokyo 1088639, Japan
[4] Kanagawa Dent Coll, Div Operat Dent & Endodont, Dept Oral Med, Yokosuka, Kanagawa 2388580, Japan
关键词
D O I
10.1074/jbc.M611181200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Periodontal ligament-associated protein-1 (PLAP-1)/asporin is a recently identified novel member of the small leucine-rich repeat proteoglycan family. PLAP-1/asporin is involved in chondrogenesis, and its involvement in the pathogenesis of osteoarthritis has been suggested. We report that PLAP-1/asporin is also expressed specifically and predominantly in the periodontal ligament (PDL) and that it negatively regulates the mineralization of PDL cells. In situ hybridization analysis revealed that PLAP-1/asporin was expressed specifically not only in the PDL of an erupted tooth but also in the dental follicle, which is the progenitor tissue of the PDL during tooth development. Overexpression of PLAP-1/asporin in mouse PDL-derived clone cells interfered with both naturally and bone morphogenetic protein 2 (BMP-2)-induced mineralization of the PDL cells. On the other hand, knockdown of PLAP-1/asporin transcript levels by RNA interference enhanced BMP-2-induced differentiation of PDL cells. Furthermore co-immuno-precipitation assays showed a direct interaction between PLAP1/asporin and BMP- 2 in vitro, and immunohistochemistry staining revealed the co-localization of PLAP-1/asporin and BMP- 2 at the cellular level. These results suggest that PLAP-1/asporin plays a specific role(s) in the periodontal ligament as a negative regulator of cytodifferentiation and mineralization probably by regulating BMP- 2 activity to prevent the periodontal ligament from developing non-physiological mineralization such as ankylosis.
引用
收藏
页码:23070 / 23080
页数:11
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