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The biocompatibility of olfactory ensheathing cells on the silk fibroin scaffolds

机译:丝素蛋白支架上嗅鞘细胞的生物相容性

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Objective: Evaluate the biocompatibility of olfactory ensheathing cells (OECs) on the electrospun low-diameter silk fibroin scaffold (LD-SFS). Methods: 400 nm silk fibroin nanofibers were prepared by electrospinning technique and were observed by scanning electron microscope (SEM). The OECs were isolated and purified by the modified differential adherent velocity method. Then, the purified OECs were seed on the poly-L-lysine and electrospun silk fibroin scaffold. The nerve growth factor receptor (NGFR) p75 and glial fibrillary acidic protein (GFAP) were used to identify OECs by immunofluorescence staining. The MTT and flow cytometric assay were used to detect the proliferation and apoptosis effect of OECs on the different scaffolds. Results: The SEM showed that the average diameter of the fibers was about 400 nm and the nanofibers constituted a three-dimensional structure with porous network and smooth surface. The morphology of OECs on the LD-SFS group was similar to that on the poly-L-lysine (PLL) group. In addition, MTT and flow cytometric assay also showed that there was no significant difference between the two scaffolds in the proliferation and apoptosis activity. Conclusion: LD-SFS may serve as an ideal tissue engineering scaffold for the olfactory ensheathing cells.
机译:目的:评价嗅鞘细胞(OECS)对电纺出低直径丝纤维素支架(LD-SFS)的生物相容性。方法:通过静电纺丝技术制备400 nm丝纤维素纳米纤维,并通过扫描电子显微镜(SEM)观察。通过改进的差分粘附速度法分离和纯化OEC。然后,将纯化的OEC在聚-L-赖氨酸和电纺丝纤维素支架上是种子。神经生长因子受体(NGFR)P75和胶质纤维酸性蛋白(GFAP)用于通过免疫荧光染色鉴定OEC。 MTT和流式细胞术测定用于检测OECS对不同支架上的增殖和凋亡作用。结果:SEM显示纤维的平均直径约为400nm,纳米纤维构成具有多孔网络和光滑表面的三维结构。 LD-SFS组的OEC的形态与聚-L-赖氨酸(PLL)组相似。此外,MTT和流式细胞术测定还表明,两种支架在增殖和凋亡活性之间没有显着差异。结论:LD-SFS可以作为嗅鞘细胞的理想组织工程支架。

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