Department of Medical Nanotechnology, Faculty of Advanced Medical Science, Tabriz University of Medical Sciences, Tabriz, Iran; Drug Applied Research Center, Tabriz University of Medical Sciences, Tabriz, Iran; Student Research Committee, Tabriz University of Medical Sciences, Tabriz, Iran.
Department of Applied Cell Sciences, Faculty of Advanced Medical Sciences, Tabriz University of Medical Sciences, Tabriz, Iran; Stem Cell Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Microvasc Res. 2021 Jan;133:104073. doi: 10.1016/j.mvr.2020.104073. Epub 2020 Sep 17.
In this study, the angiogenic capacity of human endothelial cells was studied after being plated on the surface of polyurethane-poly caprolactone (PU/PCL) scaffolds for 72 h. In this study, cells were designated into five different groups, including PU, PU/PCL (2:1), PU/PCL (1:1); PU/PCL (1:2); and PCL. Data revealed that the PU/PCL (2:1) composition had a higher modulus and breakpoint in comparison with the other groups (p < 0.05). Compared to the other groups, the PU/PCL scaffold with a molar ratio of 2:1 had lower the contact angle θ and higher tensile stress (p < 0.05). The mean size of the PU nanofibers was reduced after the addition of PCL (p < 0.05). Based on our data, the culture of endothelial cells on the surface of PU/PCL (2:1) did not cause nitrosative stress and cytotoxic effects under static conditions compared to cells plated on a conventional plastic surface (p > 0.05). Based on data from the static condition, we fabricated a tubular PU/PCL (2:1) construct for six-day dynamic cell culture inside loop air-lift bioreactors. Scanning electron microscopy showed the attachment of endothelial cells to the luminal surface of the PU/PCL scaffold. Cells were flattened and aligned under the culture medium flow. Immunofluorescence imaging showed the attachment of cells to the luminal surface indicated by blue nuclei on the luminal surface. These data demonstrated that the application of PU/PCL substrate could stimulate endothelial cells activity under static and dynamic conditions.
在这项研究中,研究了人内皮细胞在聚氨基甲酸酯-聚己内酯(PU/PCL)支架表面培养 72 小时后的血管生成能力。在这项研究中,细胞被分为五个不同的组,包括 PU、PU/PCL(2:1)、PU/PCL(1:1)、PU/PCL(1:2)和 PCL。数据显示,与其他组相比,PU/PCL(2:1)组成具有更高的模量和断点(p<0.05)。与其他组相比,摩尔比为 2:1 的 PU/PCL 支架具有更低的接触角θ和更高的拉伸应力(p<0.05)。添加 PCL 后,PU 纳米纤维的平均尺寸减小(p<0.05)。根据我们的数据,与传统塑料表面相比,在静态条件下,内皮细胞在 PU/PCL(2:1)表面培养不会引起硝化应激和细胞毒性作用(p>0.05)。根据静态条件的数据,我们制造了一个管状的 PU/PCL(2:1)构建体,用于在循环气升式生物反应器中进行为期六天的动态细胞培养。扫描电子显微镜显示内皮细胞附着在 PU/PCL 支架的管腔表面。细胞在培养基流动下被扁平化和排列。免疫荧光成像显示细胞附着在管腔表面,管腔表面上的蓝色核指示细胞附着在管腔表面。这些数据表明,PU/PCL 基底的应用可以在静态和动态条件下刺激内皮细胞的活性。