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富血小板血浆激活物联合 3D 藻酸盐支架包埋脂肪干细胞促进软骨再生。

Activated platelet-rich plasma improves cartilage regeneration using adipose stem cells encapsulated in a 3D alginate scaffold.

机构信息

Department of Cellular Biotechnology, Cell Science Research Center, Royan Institute for Biotechnology, ACECR, Isfahan, Iran.

Biomaterials Research Group, Department of Materials Engineering, Isfahan University of Technology, Isfahan, 84156-83111, Iran.

出版信息

J Tissue Eng Regen Med. 2018 Jun;12(6):1327-1338. doi: 10.1002/term.2663.

DOI:10.1002/term.2663
PMID:29522657
Abstract

In the current study, the effect of superimposing platelet-rich plasma (PRP) on different culture mediums in a three-dimensional alginate scaffold encapsulated with adipose-derived mesenchymal stem cells for cartilage tissue repair is reported. The three-dimensional alginate scaffolds with co-administration of PRP and/or chondrogenic supplements had a significant effect on the differentiation of adipose mesenchymal stem cells into mature cartilage, as assessed by an evaluation of the expression of cartilage-related markers of Sox9, collagen II, aggrecan and collagen, and glycosaminoglycan assays. For in vivo studies, following induction of osteochondral lesion in a rabbit model, a high degree of tissue regeneration in the alginate plus cell group (treated with PRP plus chondrogenic medium) compared with other groups of cell-free alginate and untreated groups (control) were observed. After 8 weeks, in the alginate plus cell group, functional chondrocytes were observed, which produced immature matrix, and by 16 weeks, the matrix and hyaline-like cartilage became completely homogeneous and integrated with the natural surrounding cartilage in the defect site. Similar effect was also observed in the subchondral bone. The cell-free scaffolds formed fibrocartilage tissue, and the untreated group did not form a continuous cartilage over the defect by 16 weeks.

摘要

在当前的研究中,报告了将富含血小板的血浆 (PRP) 叠加在三维藻酸盐支架中的不同培养基上,该支架中封装了脂肪来源的间充质干细胞,用于软骨组织修复。三维藻酸盐支架与 PRP 和/或软骨生成补充剂共同给药对脂肪间充质干细胞向成熟软骨的分化有显著影响,通过评估 Sox9、胶原 II、聚集蛋白聚糖和胶原等软骨相关标志物的表达以及糖胺聚糖测定来评估。对于体内研究,在兔模型中诱导骨软骨病变后,与其他无细胞藻酸盐组和未处理组(对照组)相比,藻酸盐加细胞组(用 PRP 加软骨生成培养基处理)中观察到高度的组织再生。8 周后,在藻酸盐加细胞组中观察到功能性软骨细胞,其产生未成熟的基质,而在 16 周时,基质和透明软骨样软骨变得完全均匀,并与缺损部位的天然周围软骨整合。在软骨下骨中也观察到了类似的效果。无细胞支架形成纤维软骨组织,而未经处理的组在 16 周时未在缺损处形成连续的软骨。

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