TGF-β3、Kartogenin和牛油果/大豆不皂化物诱导软骨形成实验与动物模型的比较

B. Hashemibeni, M. Izadi, A. Valiani, E. Esfandiari, H. Bahramian, M. Pourentezari
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摘要

背景与目的软骨组织工程是利用干细胞、支架和合适的生长因子,寻求产生天然的软骨组织来替代受损组织,解决软骨损伤治疗中存在的问题。本研究旨在比较转化生长因子β3 (TGF-β3)、Kartogenin和牛油果/大豆不皂化物(ASU)对纤维蛋白支架的影响下,脂肪源性干细胞在实验室和动物模型中的软骨分化。实验对象和方法从人脂肪组织中提取干细胞后,在实验室纤维蛋白支架上诱导成软骨分化14天。在纤维蛋白支架中分化的细胞在雄性大鼠皮下移植2周。然后,在实验室和动物模型中进行组织学和免疫组织化学研究的比较。结果动物模型中TGF-β3、Kartogenin和ASU组与实验室模型相比,甲苯胺蓝染料堆积密度明显增加。免疫组化结果显示TGF-β3组动物模型中X型胶原积累量较实验室模型明显增加。在Kartogenin和ASU组中,与实验室模型相比,动物模型中Χ型胶原蛋白的积累明显减少。结论在皮下移植前先在实验室进行分化软骨细胞的移植,有助于软骨结构的成熟和特征的完善。
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Comparison of Chondrogenesis Induction by TGF-β3, Kartogenin and Avocado/ soybean Unsaponifiables Between Laboratory and Animal Models
Background and Objectives Cartilage tissue engineering, by using stem cells, scaffolding and appropriate growth factors, seek to produce natural cartilage tissue to replace damaged tissue and solve the problems that exist in the treatment of cartilage damage. This study aims to compare chondrogenic differentiation of adipose-derived stem cells under the influence of the transforming growth factor beta 3 (TGF-β3), Kartogenin, and avocado/soybean unsaponifiables (ASU) on the fibrin scaffold in the laboratory and animal models. Subjects and Methods In this experimental laboratory study, after extraction of stem cells from human adipose tissue, induction of chondrogenic differentiation was done for 14 days on the fibrin scaffold in laboratory. The cells differentiated in the fibrin scaffold were transplanted subcutaneously under the skin of male rats for two weeks. Then, comparison of histological and immunohistochemical studies was performed in both laboratory and animal models. Results A significant increase in the density of Toluidine blue dye accumulation was observed in TGF-β3, Kartogenin and ASU groups in the animal model compared to the laboratory model. Immunohistochemical results for the collagen type X accumulation in the TGF-β3 group showed a significant increase in the animal model compared to the laboratory model. In the Kartogenin and ASU groups, the accumulation of collagen type Χ showed a significant decrease in the animal model compared to the laboratory model. Conclusion The implantation of differentiated cartilage cells in laboratory before subcutaneous transfer to the skin can help mature and complete the characteristics of the constructed cartilage.
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