Cellular and Molecular Research Center, Iran University of Medical Sciences, Tehran, Iran; Department of Medical Nanotechnology, Faculty of Advanced Technologies in Medicine, Iran University of Medical Sciences, Tehran, Iran.
Shehdad Ronak Commercialization Company (SPE, CRN 10320821698), Tehran, Iran; Department of Pharmacology and Toxicology, Faculty of Pharmacy, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Int J Biol Macromol. 2019 May 15;129:1034-1039. doi: 10.1016/j.ijbiomac.2019.02.050. Epub 2019 Feb 10.
Nowadays, regenerating peripheral nerves injuries (PNIs) remain a major clinical challenge, which has gained a great attention between scientists. Here, we represent a nanocomposite based on silk fibroin reinforced gold nanorods (SF/GNRs) to evaluate the proliferation and attachment of PC12 cells. The morphological characterization of nanocomposites with transmission electron microscopy (TEM) and Scanning electron microscopy (SEM) showed that the fabricated scaffolds have porous structure with interconnected pores that is suitable for cell adhesion and growth. GNRs significantly improved the poor electrical conductivity of bulk silk fibroin scaffold. Evaluating the morphology of PC12 cells on the scaffold also confirmed the normal morphology of cells with good rate of adhesion. SF/GNRs nanocomposites showed better cellular attachment, growth and proliferation without any toxicity compared with bulk SF scaffold. Moreover, immunostaining studies represented the overexpression of neural specific proteins like nestin and neuron specific enolase (NSE) in the cells cultured on SF/GNRs nanocomposites in comparison to neat SF scaffolds.
如今,周围神经损伤(PNI)的再生仍然是一个主要的临床挑战,这引起了科学家们的极大关注。在这里,我们提出了一种基于丝素蛋白增强金纳米棒(SF / GNRs)的纳米复合材料,以评估 PC12 细胞的增殖和附着。用透射电子显微镜(TEM)和扫描电子显微镜(SEM)对纳米复合材料的形态特征进行了表征,结果表明所制备的支架具有多孔结构,具有相互连接的孔,适合细胞附着和生长。GNRs 显著提高了块状丝素蛋白支架的电导率。对支架上 PC12 细胞形态的评估也证实了细胞具有良好的附着率和正常形态。与块状 SF 支架相比,SF / GNRs 纳米复合材料具有更好的细胞附着、生长和增殖能力,且没有任何毒性。此外,免疫染色研究表明,与纯 SF 支架相比,在 SF / GNRs 纳米复合材料上培养的细胞中神经特异性蛋白(如巢蛋白和神经元特异性烯醇化酶(NSE))的过度表达。