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机械应变促进间充质干细胞在 TiO 纳米管基底上的成骨分化。

Mechanical strain promotes osteogenic differentiation of mesenchymal stem cells on TiO nanotubes substrate.

机构信息

Shanghai Key Laboratory of Orthopaedic Implants, Department of Orthopaedics, Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, 200011, China.

Department of Orthopaedics, Yuyao People's Hospital of Zhejiang Province, Yuyao, Zhejiang, 315400, China.

出版信息

Biochem Biophys Res Commun. 2019 Apr 16;511(4):840-846. doi: 10.1016/j.bbrc.2019.02.145. Epub 2019 Mar 6.

DOI:10.1016/j.bbrc.2019.02.145
PMID:30850158
Abstract

Previous studies demonstrated cycle mechanical strain induced osteogenic differentiation of MSCs. But in general, MSCs are typically seeded on a flexible membrane or within a soft matrix. TiO nanotubes substrate topography plays a critical role in promoting the MSCs response and affects MSCs fate. Titanium implants surface modified by TiO nanotubes topography provides the opportunity to improve osseointegration by additionally regulating the MSCs fate. Titanium is one of most commonly used materials in the orthopedics and can undergo elastic deformation under certain mechanical stress. Therefore, for clinic trails, it is necessary to investigate the effect of mechanical strain on osteogenesis of MSCs on TiO nanotubes modified titanium substrate. But until now, there has been no research focused on the relationship between mechanical strain and osteogenesis of MSCs on the TiO nanotubes topography substrate. Here, we firstly applied the mechanical stress to the TiO nanotubes modified titanium specimen to investigate the effects of mechanical strain on the biological behaviors of MSCs. Our present study showed that mechanical strain promoted cell proliferation, spreading and increased vinculin expression of MSCs on the TiO nanotubes substrate. Additionally, mechanical strain enhanced the ALP activity and osteogenesis genes expression such as Runx2, BSP, ALP, OPN and OCN. Our results preliminarily demonstrated that mechanical strain enhanced the osteogenic differentiation of MSCs through the FAK-Erk1/2-Runx2 pathway on the TiO nanotubes substrate.

摘要

先前的研究表明,周期性机械应变会诱导间充质干细胞(MSCs)的成骨分化。但是,通常情况下,MSCs 是接种在柔性膜或软基质上的。TiO 纳米管基底形貌在促进 MSCs 响应方面起着关键作用,并影响 MSCs 的命运。经过 TiO 纳米管形貌表面改性的钛植入物为通过另外调节 MSCs 命运来改善骨整合提供了机会。钛是骨科中最常用的材料之一,在一定的机械应力下可以发生弹性变形。因此,对于临床研究,有必要研究机械应变对 TiO 纳米管修饰钛基底上 MSCs 成骨的影响。但是到目前为止,还没有研究集中在机械应变与 TiO 纳米管形貌基底上 MSCs 成骨之间的关系。在这里,我们首先将机械应力施加到 TiO 纳米管修饰的钛标本上,以研究机械应变对 MSCs 生物学行为的影响。我们的研究表明,机械应变促进了 MSCs 在 TiO 纳米管基底上的增殖、铺展和 vinculin 表达。此外,机械应变增强了碱性磷酸酶(ALP)活性和成骨基因的表达,如 Runt 相关转录因子 2(Runx2)、骨涎蛋白(BSP)、碱性磷酸酶(ALP)、骨桥蛋白(OPN)和骨钙素(OCN)。我们的结果初步表明,机械应变通过 FAK-Erk1/2-Runx2 通路增强了 MSCs 在 TiO 纳米管基底上的成骨分化。

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