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表面化学改性聚己内酯支架对人脱落乳牙干细胞成骨分化的影响。

Effect of surface chemistry-modified polycaprolactone scaffolds on osteogenic differentiation of stem cells from human exfoliated deciduous teeth.

机构信息

School of Materials Science and Innovation, Faculty of Science, Mahidol University, Bangkok, Thailand.

Department of Orthodontics, Faculty of Dentistry, Mahidol University, Bangkok, Thailand.

出版信息

Eur J Oral Sci. 2021 Apr;129(2):e12766. doi: 10.1111/eos.12766. Epub 2021 Mar 5.

Abstract

The aim of this study was to investigate the effect of surface modification of a polycaprolactone scaffold on promoting osteogenic differentiation of stem cells from human exfoliated deciduous teeth. Four different polycaprolactone scaffold were evaluated: untreated; coated with hyaluronic acid; coated with gelatin; and coated with hyaluronic acid and then with gelatin. The resulting scaffolds were characterized using scanning electron microscopy and attenuated total reflectance-Fourier transform infrared spectroscopy (ATR-FTIR). Human stem cells were cultured on the modified scaffolds placed in osteogenic differentiation medium. During culture, the osteogenic potential of the stem cells was examined by evaluating alkaline phosphatase activity and staining intensity, expression of osteoblastic-specific genes, and matrix mineralization. Scanning electron microscopy and ATR-FTIR confirmed productive biomacromolecular surface treatment of the polycaprolactone scaffold. All scaffolds permitted differentiation of stem cells into osteoblastic cells, but the gelatin-coated polycaprolactone scaffold facilitated osteogenesis of a larger number of stem cells than the untreated and the hyaluronic acid-coated scaffolds. We demonstrate that gelatin is an appropriate macromolecule for modifying the surface of an electrospun polycaprolactone fibre scaffold that is used subsequently in bone tissue engineering applications.

摘要

本研究旨在探讨聚己内酯支架表面改性对促进人乳牙脱落干细胞成骨分化的影响。评估了四种不同的聚己内酯支架:未处理的、涂有透明质酸的、涂有明胶的、以及先涂有透明质酸再涂有明胶的。使用扫描电子显微镜和衰减全反射傅里叶变换红外光谱(ATR-FTIR)对所得支架进行了表征。将改性后的支架置于成骨分化培养基中培养人干细胞。在培养过程中,通过评估碱性磷酸酶活性和染色强度、成骨细胞特异性基因的表达以及基质矿化,来检测干细胞的成骨潜能。扫描电子显微镜和 ATR-FTIR 证实了聚己内酯支架的生物大分子表面处理是有效的。所有支架均允许干细胞分化为成骨细胞,但涂有明胶的聚己内酯支架比未处理的和涂有透明质酸的支架更有利于更多数量的干细胞成骨。我们证明明胶是一种合适的大分子,可以修饰随后用于骨组织工程应用的静电纺丝聚己内酯纤维支架的表面。

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