Faculty of Engineering, Department of Metallurgical and Materials Engineering, Manisa Celal Bayar University, Muradiye Campus, Manisa, 45140, Turkey.
Faculty of Science and Literature, Department of Biology, Manisa Celal Bayar University, Muradiye Campus, Manisa, 45140, Turkey.
Appl Biochem Biotechnol. 2018 Dec;186(4):972-989. doi: 10.1007/s12010-018-2758-7. Epub 2018 May 25.
Graphene-containing 13-93 bioactive glass and poly(ε-caprolactone)-based bilayer, electrically conductive scaffolds were prepared for osteochondral tissue repair. Biological response of osteoblastic MC3T3-E1 and chondrogenic ATDC5 cells to the composite scaffolds was assessed under mono-culture and co-culture conditions. Cytotoxicity was investigated using MTT assay, cartilage matrix production was evaluated by Alcian blue staining, and mineralization of both types of cells in the different culture systems was observed by Alizarin red S staining. Results showed that osteoblastic and chondrogenic cells utilized in the study did not show toxic response to the prepared scaffolds under mono-culture conditions and higher cell viability rates were obtained in co-culture conditions. Larger mineralized areas were determined under co-culture conditions and calcium deposition amount significantly increased compared with that in control group samples after 21 days. Additionally, the amount of glycosaminoglycans synthesized in co-culture was higher compared to mono-culture conditions. Electric stimulation applied under mono-culture conditions suppressed the viability of MC3T3-E1 cells whereas it enhanced the viability rates of ATDC5 cells. The study suggests that the designed bilayered osteochondral constructs have the potential for osteochondral defect repair.
用于骨软骨组织修复的含石墨烯的 13-93 生物活性玻璃和聚(ε-己内酯)基双层导电支架已被制备。在单一培养和共培养条件下,评估成骨细胞 MC3T3-E1 和软骨细胞 ATDC5 对复合支架的生物反应。通过 MTT 测定法研究细胞毒性,通过茜素红 S 染色观察不同培养系统中两种细胞的矿化,通过阿尔新蓝染色评估软骨基质的产生。结果表明,研究中使用的成骨细胞和软骨细胞在单一培养条件下对制备的支架没有产生毒性反应,并且在共培养条件下获得了更高的细胞活力率。在共培养条件下确定了更大的矿化区域,并且与对照组样品相比,在 21 天后钙沉积量显著增加。此外,共培养条件下合成的糖胺聚糖量高于单一培养条件。在单一培养条件下施加的电刺激抑制了 MC3T3-E1 细胞的活力,而增强了 ATDC5 细胞的活力率。该研究表明,设计的双层骨软骨构建体具有修复骨软骨缺损的潜力。