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分层微纳拓扑结构通过整合素α2-磷脂酰肌醇-3-激酶-蛋白激酶B信号轴促进细胞黏附和成骨分化。

Hierarchical Micro-Nano Topography Promotes Cell Adhesion and Osteogenic Differentiation via Integrin α2-PI3K-AKT Signaling Axis.

作者信息

Zheng Huimin, Tian Yujuan, Gao Qian, Yu Yingjie, Xia Xianyou, Feng Zhipeng, Dong Feng, Wu Xudong, Sui Lei

机构信息

Department of Prosthodontics, School and Hospital of Stomatology, Tianjin Medical University, Tianjin, China.

Department of Cell Biology, 2011 Collaborative Innovation Center of Tianjin for Medical Epigenetics, Tianjin Key Laboratory of Medical Epigenetics, Tianjin Medical University, Tianjin, China.

出版信息

Front Bioeng Biotechnol. 2020 May 19;8:463. doi: 10.3389/fbioe.2020.00463. eCollection 2020.

Abstract

Surface topography dictates important aspects of cell biological behaviors. In our study, hierarchical micro-nano topography (SLM-AHT) with micro-scale grooves and nano-scale pores was fabricated and compared with smooth topography (S) and irregular micro-scale topography (SLA) surfaces to investigate mechanism involved in cell-surface interactions. Integrin α2 had a higher expression level on SLM-AHT surface compared with S and SLA surfaces, and the expression levels of osteogenic markers icluding Runx2, Col1a1, and Ocn were concomitantly upregulated on SLM-AHT surface. Moreover, formation of mature focal adhesions were significantly enhanced in SLM-AHT group. Noticablely, silencing integrin α2 could wipe out the difference of osteogenic gene expression among surfaces with different topography, indicating a crucial role of integrin α2 in topography induced osteogenic differentiation. In addition, PI3K-AKT signaling was proved to be regulated by integrin α2 and consequently participate in this process. Taken together, our findings illustrated that integrin α2-PI3K-AKT signaling axis plays a key role in hierarchical micro-nano topography promoting cell adhesion and osteogenic differentiation.

摘要

表面形貌决定了细胞生物学行为的重要方面。在我们的研究中,制备了具有微米级凹槽和纳米级孔隙的分级微纳形貌(SLM-AHT),并将其与光滑形貌(S)和不规则微米级形貌(SLA)表面进行比较,以研究细胞-表面相互作用的机制。与S和SLA表面相比,整合素α2在SLM-AHT表面具有更高的表达水平,并且包括Runx2、Col1a1和Ocn在内的成骨标志物的表达水平在SLM-AHT表面同时上调。此外,SLM-AHT组中成熟粘着斑的形成显著增强。值得注意的是,沉默整合素α2可以消除不同形貌表面之间成骨基因表达的差异,表明整合素α2在形貌诱导的成骨分化中起关键作用。此外,PI3K-AKT信号通路被证明受整合素α2调节,因此参与了这一过程。综上所述,我们的研究结果表明,整合素α2-PI3K-AKT信号轴在分级微纳形貌促进细胞粘附和成骨分化中起关键作用。

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