首页|明胶或聚多巴胺修饰的聚己内酯电纺膜对MC3T3-E1细胞生物学行为及成骨分化的影响

明胶或聚多巴胺修饰的聚己内酯电纺膜对MC3T3-E1细胞生物学行为及成骨分化的影响

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目的:比较明胶(Gel)和聚多巴胺(PDA)分别修饰聚己内酯(PCL)后对成骨细胞生物学行为和成骨功能的差异.方法:利用静电纺丝技术制备PCL电纺膜,化学自组装技术于PCL表面分别修饰Gel、PDA,记为G/PCL和D/PCL,用扫描电子显微镜(SEM)、傅里叶红外光谱(FTIR)、X线光电子能谱(XPS)、接触角测量仪等测定表征电纺膜的理化性能.通过SEM,免疫荧光染色后共聚焦显微镜观察MC3T3-El细胞在2种材料上的黏附形态,CCK-8试剂法检测细胞1、3、5 d增殖情况,碱性磷酸酶、茜素红染色及实时荧光定量PCR检测成骨基因表达水平.结果:D/PCL膜表面有PDA颗粒涂覆层,FTIR和XPS显示Gel与PDA的特征峰,接触角测量G/PCL和D/PCL未见明显液滴.G/PCL组细胞密度较高,黏附形态好,伪足明显.细胞增殖结果显示G/PCL组最高(P<0.05).碱性磷酸酶和茜素红染色中D/PCL组的颜色深于其余2组.qRT-PCR结果显示D/PCL组ALP、COL-1、RUNX2、OCN成骨相关基因表达较其余两组明显提高.结论:Gel和PDA修饰均可提升PCL支架的细胞黏附、增殖和成骨性能,Gel修饰提升增殖作用更明显,PDA修饰提升成骨作用更显著.
The effects of gelatin or polydopamine-modified poly caprolactone electrospun membranes on the biological behavior and osteogenic differentiation of MC3T3-E1 cells
Objective:To compare the effects of gelatin(Gel)and polydopamine(PDA)modification of polycaprolactone(PCL)on the biological behaviour and osteogenic function of osteoblasts.Methods:PCL electrospun membranes were prepared by electrostatic spinning technique,PCL surface was modified by Gel and PDA respectively as G/PCL and D/PCL with chemical self-assembly tech-nique,and the physicochemical properties of the electrospun membranes were characterized by scanning electron microscopy(SEM),Fourier infrared spectroscopy(FTIR),X-ray photoelectron spectroscope(XPS)and contact angle measurement.The MC3T3-E1 cell adhesion morphology was observed by SEM,immunofluorescence staining followed by confocal microscopy(CLSM),cell proliferation at 1,3 and 5 d was tested by CCK-8 assay,alkaline phosphatase(ALP)staining,alizarin red staining and qRT-PCR were used to detect osteogenic gene expression of the cells.Results:A coating of PDA particles was observed on the surface of D/PCL film.FTIR and XPS showed that the characteristic peaks of Gel and PDA,and there was no obvious droplets on the surface of G/PCL and D/PCL ob-served by contact angle test.Cell density of G/PCL group was higher,the adhesion morphology was good and pseudopods were obvi-ous.CCK-8 assay showed the highest proliferation of the cells on G/PCL(P<0.05).ALP and alizarin red staining of the cells were stronger in D/PCL group than in the other 2 groups.qRT-PCR results showed that the mRNA expression of ALP,COL-1,RUNX2 and OCN was higher in the D/PCL group than in the other 2 groups.Conclusion:Both Gel and PDA modification can enhance the cell adhesion,proliferation and osteogenic properties of PCL scaffolds,Gel modification may induce a more pronounced proliferative effect and PDA modification more pronounced osteogenic effect.

Poly caprolactoneGelatinDopamineOsteogenesis

谢泽宇、林彦吟、王鸿、赖颖真

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361023,厦门医学院口腔医学系·口腔生物材料福建省高校工程研究中心

聚己内酯 明胶 聚多巴胺 成骨

大学生创新创业训练计划立项(国家级)福建省自然科学基金面上项目福建省教育厅本科教改专项

2021126310062022J011408FBJG20210210

2024

实用口腔医学杂志
第四军医大学口腔医学院

实用口腔医学杂志

CSTPCD北大核心
影响因子:0.942
ISSN:1001-3733
年,卷(期):2024.40(4)
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