KAIST Institute for the BioCentury, Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Republic of Korea.
Biomaterials. 2013 Mar;34(8):2017-23. doi: 10.1016/j.biomaterials.2012.11.052. Epub 2012 Dec 20.
Graphene-based nanomaterials have received much attention in biomedical applications for drug/gene delivery, cancer therapy, imaging, and tissue engineering. Despite the capacity of 2D carbon materials as a nontoxic and implantable platform, their effect on myogenic differentiation has been rarely studied. We investigated the myotube formation on graphene-based nanomaterials, particularly graphene oxide (GO) and reduced graphene oxide (rGO). GO sheets were immobilized on amine-modified glass to prepare GO-modified glass, which was further reduced by hydrazine treatment for the synthesis of rGO-modified substrate. We studied the behavior, including adhesion, proliferation, and differentiation, of mouse myoblast C2C12 on unmodified, GO-, and rGO-modified glass substrates. According to our analyses of myogenic protein expression, multinucleate myotube formation, and expression of differentiation-specific genes (MyoD, myogenin, Troponin T, and MHC), myogenic differentiation was remarkably enhanced on GO, which resulted from serum protein adsorption and nanotopographical cues. Our results demonstrate the ability of GO to stimulate myogenic differentiation, showing a potential for skeletal tissue engineering applications.
基于石墨烯的纳米材料在药物/基因递送、癌症治疗、成像和组织工程等生物医学应用中受到了广泛关注。尽管二维碳材料作为一种无毒和可植入的平台具有很大的潜力,但它们对成肌分化的影响很少被研究。我们研究了基于石墨烯的纳米材料,特别是氧化石墨烯(GO)和还原氧化石墨烯(rGO)对肌管形成的影响。GO 片被固定在氨基修饰的玻璃上,以制备 GO 修饰的玻璃,然后通过水合肼处理进一步还原,以合成 rGO 修饰的基底。我们研究了未修饰、GO-和 rGO-修饰的玻璃基底上小鼠成肌细胞 C2C12 的行为,包括黏附、增殖和分化。根据我们对肌球蛋白表达、多核肌管形成以及分化特异性基因(MyoD、myogenin、肌钙蛋白 T 和 MHC)表达的分析,GO 显著促进了成肌分化,这归因于血清蛋白吸附和纳米形貌线索。我们的结果表明 GO 具有刺激成肌分化的能力,为骨骼组织工程应用提供了潜力。