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来自培养的软骨样组织的细胞外基质粉末作为软骨修复的细胞载体。

Extracellular matrix powder from cultured cartilage-like tissue as cell carrier for cartilage repair.

作者信息

Teng Yingying, Li Xiupeng, Chen Yafang, Cai Hanxu, Cao Wanxu, Chen Xuening, Sun Yong, Liang Jie, Fan Yujiang, Zhang Xingdong

机构信息

National Engineering Research Center for Biomaterials, Sichuan University, 29 Wangjiang Road, Chengdu, 610064, China.

出版信息

J Mater Chem B. 2017 May 14;5(18):3283-3292. doi: 10.1039/c7tb00640c. Epub 2017 Apr 24.

Abstract

Cartilage extracellular matrix (ECM) is a promising material for cartilage repair because of its bioactivity. However, the animal source of ECM unavoidably increases the risk of pathogen infection and the variability of product quality. In this study, we utilized a novel 3D culture method to prepare a new type of artificial decellularized matrix powder (DEMP) for the development of injectable, bioactive, biodegradable cell carriers for cartilage tissue engineering. This culture method combined hanging drop culture with suspension culture method, and was very efficient to produce cartilage-like tissue (CLT). By this method, an initial 2.3 × 10 chondrocyte generated as much as 58.22 mg wet weight CLT at two weeks, which proved to contain abundant glycoaminoglycans (GAGs), type II collagen, and BMP-2 and TGF-β1 growth factors by staining techniques and biochemical analysis. Subsequently, the two-week-old CLT was decellularized to prepare the artificial DEMP. In an in vitro study, it was found that MSCs cultured on DEMP differentiated to chondrocytes very well and secreted rich GAGs and type II collagen at three weeks even without exogenous TGF-β1. The in vivo study demonstrated that the DEMP not only facilitated regeneration of hyaline cartilage, which was implied by the intense staining of GAGs and type II collagen in rabbit subchondral defects at 1 month, but also benefited the regeneration of subchondral bone (bone ingrowth at 1 month: 48.22%) as shown in micro-CT data. Collectively, these results suggest that the artificial DEMP prepared by this culture method holds great potential as a novel ECM material for cartilage repair.

摘要

软骨细胞外基质(ECM)因其生物活性而成为软骨修复的一种有前景的材料。然而,ECM的动物来源不可避免地增加了病原体感染的风险和产品质量的变异性。在本研究中,我们利用一种新型的三维培养方法制备了一种新型的人工脱细胞基质粉末(DEMP),用于开发用于软骨组织工程的可注射、生物活性、可生物降解的细胞载体。这种培养方法将悬滴培养与悬浮培养方法相结合,能非常高效地产生软骨样组织(CLT)。通过这种方法,最初的2.3×10个软骨细胞在两周时产生了多达58.22毫克湿重的CLT,通过染色技术和生化分析证明其含有丰富的糖胺聚糖(GAGs)、II型胶原蛋白以及骨形态发生蛋白-2(BMP-2)和转化生长因子-β1(TGF-β1)生长因子。随后,将两周龄的CLT进行脱细胞处理以制备人工DEMP。在一项体外研究中发现,在DEMP上培养的间充质干细胞(MSCs)能很好地分化为软骨细胞,即使在没有外源性TGF-β1的情况下,三周时也能分泌丰富的GAGs和II型胶原蛋白。体内研究表明,DEMP不仅促进了透明软骨的再生,1个月时兔软骨下缺损处GAGs和II型胶原蛋白的强烈染色表明了这一点,而且如微型计算机断层扫描(micro-CT)数据所示,还有利于软骨下骨的再生(1个月时骨长入:48.22%)。总体而言,这些结果表明,通过这种培养方法制备的人工DEMP作为一种用于软骨修复的新型ECM材料具有巨大潜力。

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