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在纤维蛋白和纤维蛋白-藻酸盐支架中,比较派斯克莱定和转化生长因子β1对人脂肪来源干细胞软骨分化的功效。

Comparison of the efficacy of piascledine and transforming growth factor β1 on chondrogenic differentiation of human adipose-derived stem cells in fibrin and fibrin-alginate scaffolds.

作者信息

Hashemibeni Batool, Valiani Ali, Esmaeli Mojtaba, Kazemi Mohammad, Aliakbari Maryam, Iranpour Farhad Golshan

机构信息

Department of Anatomical Sciences, Medical School, Isfahan University of Medical Sciences, Isfahan, Iran.

Department of Molecular Biology, Medical School, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

Iran J Basic Med Sci. 2018 Feb;21(2):212-218. doi: 10.22038/IJBMS.2018.24693.6136.

Abstract

OBJECTIVES

The aim of this study was to compare the chondrogenic induction potential of Piascledine and TGF-β1 on adipose-derived stem cells (ADSCs) in fibrin and fibrin-alginate scaffolds.

MATERIALS AND METHODS

Human subcutaneous adipose tissues were harvested from three patients who were scheduled to undergo liposuction. Isolated ADSCs were proliferated in a culture medium. Then, the cells were seeded in fibrin or fibrin-alginate scaffolds and cultured for 14 days in a chondrogenic medium containing Piascledine, TGF-β1, or both. The rate of cell proliferation and survival was evaluated by using MTT [3-(4, 5-dimethylthiazolyl-2)-2, 5-diphenyltetrazolium bromide] assay and the rate of the expression of type II collagen, aggrecan, and type X collagen genes was evaluated by real-time polymerase chain reaction (real-time PCR) method.

RESULTS

The MTT results showed that Piascledine is able to enhance the proliferation and survival of ADSCs in fibrin scaffolds in comparison to other groups (<0.05). Real-time PCR evaluation revealed that the expression of type II collagen was higher in TGF- β1groups, but the expression of aggrecan was higher in TGF-β1 alone or along with Piascledine in fibrin-alginate scaffolds. Furthermore, the expression of type X collagen was lower in Piascledine alone or along with TGF-β1 in fibrin scaffold.

CONCLUSION

Piascledine can enhance the proliferation and differentiation of ADSCs in fibrin scaffolds.

摘要

目的

本研究旨在比较碧斯克林(Piascledine)和转化生长因子-β1(TGF-β1)对纤维蛋白和纤维蛋白-藻酸盐支架中脂肪来源干细胞(ADSCs)的软骨形成诱导潜力。

材料与方法

从三名计划进行抽脂手术的患者身上采集人皮下脂肪组织。分离出的ADSCs在培养基中增殖。然后,将细胞接种到纤维蛋白或纤维蛋白-藻酸盐支架中,并在含有碧斯克林、TGF-β1或两者的软骨形成培养基中培养14天。通过MTT [3-(4, 5-二甲基噻唑-2)-2, 5-二苯基四氮唑溴盐] 法评估细胞增殖和存活速率,并通过实时聚合酶链反应(实时PCR)法评估II型胶原蛋白、聚集蛋白聚糖和X型胶原蛋白基因的表达速率。

结果

MTT结果显示,与其他组相比,碧斯克林能够增强纤维蛋白支架中ADSCs的增殖和存活(<0.05)。实时PCR评估显示,TGF-β1组中II型胶原蛋白的表达较高,但在纤维蛋白-藻酸盐支架中,单独使用TGF-β1或与碧斯克林联合使用时,聚集蛋白聚糖的表达较高。此外,在纤维蛋白支架中,单独使用碧斯克林或与TGF-β1联合使用时,X型胶原蛋白的表达较低。

结论

碧斯克林可增强纤维蛋白支架中ADSCs的增殖和分化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/217d/5811761/fcb55fc849c5/IJBMS-21-212-g001.jpg

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