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水解鱼胶原蛋白诱导马脂肪组织来源基质细胞的软骨分化。

Hydrolyzed fish collagen induced chondrogenic differentiation of equine adipose tissue-derived stromal cells.

机构信息

Institute of Veterinary Anatomy, Histology, and Embryology, Justus-Liebig University of Giessen, Giessen, Germany.

出版信息

Histochem Cell Biol. 2010 Dec;134(6):545-54. doi: 10.1007/s00418-010-0760-4. Epub 2010 Nov 14.

Abstract

Adipose-derived stromal cells (ADSCs) are multipotent cells which, in the presence of appropriate stimuli, can differentiate into various lineages such as the osteogenic, adipogenic and chondrogenic. In this study, we investigated the effect of transforming growth factor beta 1 (TGF-β1) in comparison to hydrolyzed fish collagen in terms of the chondrogenic differentiation potential of ADSCs. ADSCs were isolated from subcutaneous fat of horses by liposuction. Chondrogenesis was investigated using a pellet culture system. The differentiation medium was either supplemented with TGF-β1 (5 ng/ml) or fish collagen (0.5 mg/ml) for a 3 week period. After the 3 weeks in vitro differentiation, RT-PCR and histological staining for proteoglycan synthesis and type II collagen were performed to evaluate the degree of chondrogenic differentiation and the formation of cartilaginous extracellular matrix (ECM). The differentiation of ADSCs induced by TGF-β1 showed a high expression of glycosaminoglycan (GAG). Histological analysis of cultures stimulated by hydrolyzed fish collagen demonstrated an even higher GAG expression than cultures stimulated under standard conditions by TGF-β1. The expression of cartilage-specific type II collagen and Sox9 was about the same in both stimulated cultures. In this study, chondrogenesis was as effectively induced by hydrolyzed fish collagen as it was successfully induced by TGF-β1. These findings demonstrated that hydrolyzed fish collagen alone has the potential to induce and maintain ADSCs-derived chondrogenesis. These results support the application of ADSCs in equine veterinary tissue engineering, especially for cartilage repair.

摘要

脂肪来源的基质细胞(ADSCs)是多能细胞,在适当的刺激下,可以分化为成骨细胞、脂肪细胞和成软骨细胞等多种谱系。在这项研究中,我们研究了转化生长因子β 1(TGF-β1)与水解鱼胶原蛋白在诱导 ADSCs 软骨分化潜能方面的作用。ADSCs 是通过吸脂术从马的皮下脂肪中分离出来的。采用微球培养系统研究软骨分化。分化培养基分别补充 TGF-β1(5ng/ml)或水解鱼胶原蛋白(0.5mg/ml),培养 3 周。体外分化 3 周后,通过 RT-PCR 和组织化学染色检测糖胺聚糖(GAG)合成和 II 型胶原的表达,以评估软骨分化程度和软骨细胞外基质(ECM)的形成。TGF-β1 诱导的 ADSCs 分化表现出高表达的糖胺聚糖(GAG)。用水解鱼胶原蛋白刺激培养物的组织学分析表明,其 GAG 表达比 TGF-β1 标准条件下刺激的培养物更高。两种刺激培养物中软骨特异性 II 型胶原和 Sox9 的表达大致相同。在这项研究中,水解鱼胶原蛋白可有效诱导软骨生成,与 TGF-β1 诱导的效果相当。这些发现表明,水解鱼胶原蛋白具有诱导和维持 ADSCs 来源软骨形成的潜力。这些结果支持 ADSCs 在马兽医组织工程中的应用,特别是用于软骨修复。

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