Li Jingan, Qin Wei, Zhang Kun, Wu Feng, Yang Ping, He Zikun, Zhao Ansha, Huang Nan
Key Lab. for Advanced Technologies of Materials, Ministry of Education, School of Material Science and Engineering, Southwest Jiaotong University, Chengdu 610031, PR China.
Key Lab. for Advanced Technologies of Materials, Ministry of Education, School of Material Science and Engineering, Southwest Jiaotong University, Chengdu 610031, PR China; Heze Alliancells Bioscience Co., Ltd., Changzhou 213000, PR China.
Colloids Surf B Biointerfaces. 2016 Sep 1;145:410-419. doi: 10.1016/j.colsurfb.2016.05.024. Epub 2016 May 11.
Building healthy and oriented smooth muscle cells (SMCs) environment is an effective method for improving the surface endothelialization of the cardiovascular implants. However, a long-term and stable source of SMCs for implantation without immune rejection and inflammation has not been solved, and mesenchymal stem cells (MSCs) differentiation may be a good choice. In this work, two types of TiO2 micro/nano interfaces were fabricated on titanium surface by photolithography and anodic oxidation. These TiO2 micro/nano interfaces were used to regulate the differentiation of the MSCs. The X-ray diffraction (XRD) detection showed that the TiO2 micro/nano interfaces possessed the anatase crystal structure, suggesting good cytocompatibility. The CCK-8 results indicated the TiO2 micro/nano interfaces improved MSC proliferation, further immunofluorescence staining and calculation of the cell morphology index proved the micro/nano surfaces also elongated MSCs and regulated MSCs oriented growth. The specific staining of α-SMA, CNN-1, vWF, CD44 and CD133 markers revealed that the micro/nano surfaces induced MSCs differentiation to contractile SMCs, and the endothelial cells (ECs) culture experiment indicated that the MSCs induced by micro/nano interfaces contributed to the ECs attachment and proliferation. This method will be further studied and applied for the surface modification of the cardiovascular implants.
构建健康且定向的平滑肌细胞(SMC)环境是改善心血管植入物表面内皮化的有效方法。然而,用于植入且无免疫排斥和炎症的长期稳定的SMC来源尚未得到解决,间充质干细胞(MSC)分化可能是一个不错的选择。在这项工作中,通过光刻和阳极氧化在钛表面制备了两种类型的TiO2微/纳米界面。这些TiO2微/纳米界面用于调节MSC的分化。X射线衍射(XRD)检测表明,TiO2微/纳米界面具有锐钛矿晶体结构,表明具有良好的细胞相容性。CCK-8结果表明,TiO2微/纳米界面促进了MSC的增殖,进一步的免疫荧光染色和细胞形态指数计算证明,微/纳米表面还使MSC伸长并调节了MSC的定向生长。α-SMA、CNN-1、vWF、CD44和CD133标志物的特异性染色显示,微/纳米表面诱导MSC分化为收缩性SMC,内皮细胞(EC)培养实验表明,微/纳米界面诱导的MSC有助于EC的附着和增殖。该方法将进一步研究并应用于心血管植入物的表面改性。