Lasocka Iwona, Szulc-Dąbrowska Lidia, Skibniewski Michał, Skibniewska Ewa, Gregorczyk-Zboroch Karolina, Pasternak Iwona, Hubalek Kalbacova Marie
Department of Biology of Animal Environment, Institute of Animal Science, Warsaw University of Life Sciences, 02-786 Warsaw, Poland.
Department of Preclinical Sciences, Institute of Veterinary Medicine, Warsaw University of Life Sciences, 02-786 Warsaw, Poland.
Materials (Basel). 2021 Jan 30;14(3):643. doi: 10.3390/ma14030643.
This study investigates the effect of graphene scaffold on morphology, viability, cytoskeleton, focal contacts, mitochondrial network morphology and activity in BALB/3T3 fibroblasts and provides new data on biocompatibility of the "graphene-family nanomaterials". We used graphene monolayer applied onto glass cover slide by electrochemical delamination method and regular glass cover slide, as a reference. The morphology of fibroblasts growing on graphene was unaltered, and the cell viability was 95% compared to control cells on non-coated glass slide. There was no significant difference in the cell size (spreading) between both groups studied. Graphene platform significantly increased BALB/3T3 cell mitochondrial activity (WST-8 test) compared to glass substrate. To demonstrate the variability in focal contacts pattern, the effect of graphene on vinculin was examined, which revealed a significant increase in focal contact size comparing to control-glass slide. There was no disruption in mitochondrial network morphology, which was branched and well connected in relation to the control group. Evaluation of the JC-1 red/green fluorescence intensity ratio revealed similar levels of mitochondrial membrane potential in cells growing on graphene-coated and uncoated slides. These results indicate that graphene monolayer scaffold is cytocompatible with connective tissue cells examined and could be beneficial for tissue engineering therapy.
本研究调查了石墨烯支架对BALB/3T3成纤维细胞的形态、活力、细胞骨架、黏着斑、线粒体网络形态及活性的影响,并提供了有关“石墨烯家族纳米材料”生物相容性的新数据。我们使用通过电化学剥离法施加在玻璃盖玻片上的石墨烯单层以及普通玻璃盖玻片作为对照。生长在石墨烯上的成纤维细胞形态未改变,与未镀膜玻璃玻片上的对照细胞相比,细胞活力为95%。所研究的两组细胞大小(铺展情况)无显著差异。与玻璃基质相比,石墨烯平台显著提高了BALB/3T3细胞的线粒体活性(WST-8检测)。为了证明黏着斑模式的变异性,研究了石墨烯对纽蛋白的影响,结果显示与对照玻璃玻片相比,黏着斑大小显著增加。线粒体网络形态没有破坏,与对照组相比,其呈分支状且连接良好。对JC-1红/绿荧光强度比值的评估显示,生长在涂有石墨烯和未涂石墨烯玻片上的细胞中线粒体膜电位水平相似。这些结果表明,石墨烯单层支架与所检测的结缔组织细胞具有细胞相容性,可能对组织工程治疗有益。