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PLAP-1/抑涎蛋白,一种新型的牙周膜矿化负调节因子。

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

作者信息

Yamada Satoru, Tomoeda Miki, Ozawa Yasuhiro, Yoneda Shinya, Terashima Yoshimitsu, Ikezawa Kazuhiko, Ikegawa Shiro, Saito Masahiro, Toyosawa Satoru, Murakami Shinya

机构信息

Department of Periodontology, Osaka University Graduate School of Dentistry, Suita, Osaka 565-0871, Japan.

出版信息

J Biol Chem. 2007 Aug 10;282(32):23070-80. doi: 10.1074/jbc.M611181200. Epub 2007 May 23.

Abstract

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-immunoprecipitation assays showed a direct interaction between PLAP-1/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.

摘要

牙周韧带相关蛋白-1(PLAP-1)/天冬氨酸富含亮氨酸小分子重复蛋白聚糖是最近鉴定出的富含亮氨酸小分子重复蛋白聚糖家族的新成员。PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖参与软骨形成,并且有人提出它参与骨关节炎的发病机制。我们报告称,PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖也特异性且主要在牙周韧带(PDL)中表达,并且它对PDL细胞的矿化起负调节作用。原位杂交分析显示,PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖不仅在萌出牙齿的PDL中特异性表达,而且在牙囊(牙齿发育过程中PDL的祖细胞组织)中也特异性表达。在小鼠PDL来源的克隆细胞中过表达PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖会干扰PDL细胞的自然矿化以及骨形态发生蛋白2(BMP-2)诱导的矿化。另一方面,通过RNA干扰降低PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖的转录水平可增强BMP-2诱导的PDL细胞分化。此外,免疫共沉淀分析表明PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖与BMP-2在体外存在直接相互作用,免疫组织化学染色显示PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖与BMP-2在细胞水平上共定位。这些结果表明,PLAP-1/天冬氨酸富含亮氨酸小分子重复蛋白聚糖可能通过调节BMP-2活性,作为细胞分化和矿化的负调节因子在牙周韧带中发挥特定作用,以防止牙周韧带发生诸如骨粘连等非生理性矿化。

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