首页> 美国卫生研究院文献>Journal of Cellular and Molecular Medicine >MicroRNA‐181a/b‐1‐encapsulated PEG/PLGA nanofibrous scaffold promotes osteogenesis of human mesenchymal stem cells
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MicroRNA‐181a/b‐1‐encapsulated PEG/PLGA nanofibrous scaffold promotes osteogenesis of human mesenchymal stem cells

机译:MicroRNA-181A / B-1封装的PEG / PLGA纳米纤维支架促进人间充质干细胞的骨质发生

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摘要

Bioactive nanofibres play a useful role in increasing the efficiency of tissue engineering scaffolds. MicroRNAs (miRs) alone, and in combination with tissue engineering scaffolds, can be effective in treating bone fractures and osteoporosis by regulating many post‐transcriptional cellular pathways. Herein, miR‐181a/b‐1 was incorporated in the electrospun poly (lactic‐co‐glycolic acid) (PLGA) nanofibres (PLGA‐miR). After characterization scaffolds, the osteoinductive capacity of the nanofibres was investigated when adipose‐derived mesenchymal stem cells (AT‐MSCs) were cultured on the PLGA and PLGA‐miR nanofibres. miR incorporating in the nanofibres has not any significant effect on the size and morphology of the nanofibres, but its biocompatibility was increased significantly compared to the empty nanofibres. Alkaline phosphatase (ALP) activity and calcium measures were evaluated as two important osteogenic markers, and the results revealed that the highest measures were observed in the AT‐MSCs cultured on PLGA‐miR nanofibres. Detected ALP activity and calcium measures in miR‐transduced AT‐MSCs cultured on TCPS were also significantly higher than AT‐MSCs cultured on PLGA and TCPS groups. The highest expression levels of bone‐related genes were observed in the AT‐MSCs cultured on PLGA‐miR nanofibres. This improvement in the osteogenic differentiation potential of the AT‐MSCs was also confirmed by evaluating osteopontin protein in the cells cultured on PLGA‐miR. It can be concluded that miR‐181a/b‐1 has a significant impact on the AT‐MSC osteogenic differentiation, and this impact synergistically increased when incorporated in the PLGA nanofibres.
机译:生物活性纳米纤维在增加组织工程支架效率方面发挥了有用作用。单独的MicroRNAS(MIRS),并与组织工程支架组合,可通过调节许多转录后细胞途径来治疗骨折和骨质疏松症。在此,MIR-181A / B-1掺入ElectromatOP聚(乳酸 - 共乙醇酸)(PLGA)纳米纤维(PLGA-miR)中。在表征支架后,当在PLGA和PLGA-miR纳米纤维上培养脂肪衍生的间充质干细胞(AT-MSC)时,研究了纳米纤维的骨诱导能力。纳米纤维中的miR对纳米纤维的大小和形态没有任何显着影响,但与空纳米纤维相比,其生物相容性显着增加。碱性磷酸酶(ALP)活性和钙措施被评价为两个重要的骨质原子油标记物,结果表明,在PLGA-MIR纳米纤维上培养的AT-MSCs中观察到最高措施。检测到在TCP培养的MIR转导的ALP活性和钙措施也显着高于在PLGA和TCPS组上培养的MSC。在PLGA-miR纳米纤维上培养的AT-MSCs中观察到骨相关基因的最高表达水平。通过在PLGA-MIR上培养的细胞中评价骨偶联蛋白蛋白,还通过评估骨桥蛋白蛋白来证实AT-MSCs的骨质发生分化电位的这种改善。可以得出结论,miR-181a / b-1对AT-MSC骨质发生分化产生显着影响,并且当掺入PLGA纳米纤维中时,这种冲击协同增加。

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