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纤维蛋白、琼脂糖和结冷胶水凝胶作为干细胞载体和生长因子递送微球在软骨再生中的比较。

A comparison of fibrin, agarose and gellan gum hydrogels as carriers of stem cells and growth factor delivery microspheres for cartilage regeneration.

机构信息

Trinity Centre for Bioengineering, Trinity Biomedical Sciences Institute, Trinity College Dublin, Dublin 2, Ireland.

出版信息

Biomed Mater. 2013 Jun;8(3):035004. doi: 10.1088/1748-6041/8/3/035004. Epub 2013 Mar 26.

Abstract

The limited intrinsic repair capacity of articular cartilage has led to the investigation of different treatment options to promote its regeneration. The delivery of hydrogels containing stem or progenitor cells and growth factor releasing microspheres represents an attractive approach to cartilage repair. In this study, the influence of the encapsulating hydrogel on the ability of progenitor cells coupled with TGF-β3 releasing microspheres to form cartilaginous tissue was investigated. Fibrin, agarose and gellan gum hydrogels containing TGF-β3 loaded gelatin microspheres and progenitor cells derived from the infrapatellar fat-pad of the knee were cultured for 21 days in a chemically defined media. In the presence of TGF-β3 releasing microspheres, gellan gum hydrogels were observed to facilitate greater cell proliferation than fibrin or agarose hydrogels. Histological and biochemical analysis of the hydrogels indicated that fibrin was the least chondro-inductive of the three hydrogels, while agarose and gellan gum appeared to support more robust cartilage formation as demonstrated by greater sGAG accumulation within these constructs. Gellan gum hydrogels also stained more intensely for collagen type II and collagen type I, suggesting that although total collagen synthesis was higher in these constructs, that the phenotype may be more fibrocartilaginous in nature than normal hyaline cartilage. This study demonstrates how the encapsulating hydrogel can have a significant impact on the ability of stem cells to form cartilage when incorporated into a growth factor delivery system.

摘要

关节软骨的内在修复能力有限,这促使人们研究了不同的治疗方法来促进其再生。将含有干细胞或祖细胞和生长因子释放微球的水凝胶递送至软骨部位是一种很有吸引力的软骨修复方法。在这项研究中,研究人员研究了包封水凝胶对与 TGF-β3 释放微球结合的祖细胞形成软骨组织的能力的影响。在化学定义的培养基中培养 21 天,使来自膝关节髌下脂肪垫的 TGF-β3 负载明胶微球和祖细胞包埋在纤维蛋白、琼脂糖和结冷胶水凝胶中。在 TGF-β3 释放微球的存在下,与纤维蛋白或琼脂糖水凝胶相比,结冷胶水凝胶被观察到可促进更大的细胞增殖。水凝胶的组织学和生化分析表明,纤维蛋白是三种水凝胶中诱导软骨形成能力最差的,而琼脂糖和结冷胶似乎支持更健壮的软骨形成,因为这些构建体中 sGAG 的积累更多。结冷胶水凝胶也更强烈地染色为 II 型胶原和 I 型胶原,这表明尽管这些构建体中的总胶原蛋白合成更高,但表型可能更偏向纤维软骨,而不是正常的透明软骨。这项研究表明,当将干细胞纳入生长因子递送系统时,包封水凝胶如何对干细胞形成软骨的能力产生重大影响。

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