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血管生成素样蛋白2的下调通过激活ERK1/2信号通路部分抑制成牙骨质细胞分化。

Downregulation of angiopoietin-like protein 2 inhibits cementoblast differentiation partially by activating the ERK1/2 signaling pathway.

作者信息

Jiang Chenxi, Liu Huan, Sun Hualing, Wang Xiaoxuan, Liao Haiqing, Ma Li, Cao Zhengguo

机构信息

The State Key Laboratory Breeding Base of Basic Science of Stomatology (Hubei-MOST KLOS) and Key Laboratory for Oral Biomedical Engineering of Ministry of Education (KLOBME), School and Hospital of Stomatology, Wuhan University Wuhan, China.

Department of Periodontology, School and Hospital of Stomatology, Wuhan University Wuhan, China.

出版信息

Am J Transl Res. 2019 Jan 15;11(1):314-326. eCollection 2019.

Abstract

Angiopoietin-like protein 2 (ANGPTL2) is abundantly expressed in adipose tissue, is associated with tissue homeostasis, and promotes osteoblast and chondrocyte differentiation. In teeth, cementum, a thin layer of mineralized tissue that is formed by cementoblasts, covers the entire root surface and is a vital component of periodontium. The cementoblasts regulate the deposition and mineralization of the cementum matrix. However, the effects of ANGPTL2 on cementoblast differentiation have not been studied. The objective of this study was to elucidate the role of ANGPTL2 during cementoblast differentiation and determine its underlying mechanisms. Our results showed that the expression levels of ANGPTL2 gradually increased during cementoblast differentiation. After ANGPTL2 was knocked down using short-hairpin RNA, the levels of the osteogenic markers osterix (OSX), alkaline phosphatase (ALP), bone sialoprotein (BSP), and osteocalcin (OCN) decreased. In addition, ALP activity and the number of calcified nodules were dramatically reduced compared with those in the negative control. Interestingly, the ERK1/2 signaling pathway was activated after ANGPTL2 knockdown. Treatment with PD98059, the inhibitor of the ERK1/2 signaling pathway, partially rescued the decreased differentiation capability of cementoblast caused by ANGPTL2 downregulation. Collectively, ANGPTL2 knockdown inhibited cementoblast differentiation partially by activating the ERK1/2 signaling pathway. These findings suggest that ANGPTL2 was indispensable in cementoblast differentiation.

摘要

血管生成素样蛋白2(ANGPTL2)在脂肪组织中大量表达,与组织稳态相关,并促进成骨细胞和软骨细胞分化。在牙齿中,牙骨质是由成牙骨质细胞形成的一层薄薄的矿化组织,覆盖整个牙根表面,是牙周组织的重要组成部分。成牙骨质细胞调节牙骨质基质的沉积和矿化。然而,ANGPTL2对成牙骨质细胞分化的影响尚未得到研究。本研究的目的是阐明ANGPTL2在成牙骨质细胞分化过程中的作用,并确定其潜在机制。我们的结果表明,ANGPTL2的表达水平在成牙骨质细胞分化过程中逐渐增加。使用短发夹RNA敲低ANGPTL2后,成骨标志物osterix(OSX)、碱性磷酸酶(ALP)、骨唾液蛋白(BSP)和骨钙素(OCN)的水平降低。此外,与阴性对照相比,ALP活性和钙化结节数量显著减少。有趣的是,敲低ANGPTL2后ERK1/2信号通路被激活。用ERK1/2信号通路抑制剂PD98059处理,部分挽救了由ANGPTL2下调引起的成牙骨质细胞分化能力下降。总的来说,敲低ANGPTL2通过激活ERK1/2信号通路部分抑制成牙骨质细胞分化。这些发现表明ANGPTL2在成牙骨质细胞分化中不可或缺。

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