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利用滑膜衍生间充质干细胞和可注射性凝胶多糖水凝胶构建的体外工程化软骨。

In vitro engineered cartilage using synovium-derived mesenchymal stem cells with injectable gellan hydrogels.

机构信息

Center for Stem Cell Biology and Tissue Engineering of Sun Yat-Sen University, Guangzhou 510080, China.

出版信息

Acta Biomater. 2010 Mar;6(3):1178-85. doi: 10.1016/j.actbio.2009.08.042. Epub 2009 Sep 4.

Abstract

Synovium-derived mesenchymal stem cells (SMSC), a novel line of stem cells, are regarded as a promising cell source for cartilage tissue engineering. The goal of this study was to investigate rabbit SMSC coupled with injectable gellan hydrogels for in vitro engineered cartilage. SMSC were isolated from rabbit synovial tissue, amplified to passage 4 in monolayer, and encapsulated in injectable gellan hydrogels, constructs of which were cultured in chondrogenic medium supplemented with TGF-beta1, TGF-beta3 or BMP-2 for up to 42 days. The quality of the constructs was assessed in terms of cell proliferation and chondrocytic gene/protein expression using WST-1 assay, real-time RT-PCR, biochemical analysis, histology and immunohistochemical analysis. Results indicate that the viability of SMSC in hydrogels treated with TGF-beta1, TGF-beta3 and BMP-2 remained high at culture time. The constructs formed cartilaginous tissue with the expression of chondrocytic genes (collagen type II, aggrecan, biglycan, SOX 9) and cartilaginous matrix (sulphated glycosaminoglycan and collagen) as early as 21 days in culture. Both TGF-beta1 and TGF-beta3 treated SMSC-laden hydrogels showed more chondrogenesis compared with BMP-2 treated SMSC-laden hydrogels. It demonstrates that injectable SMSC-laden gels, when treated with TGF-beta1, TGF-beta3 or BMP-2, are highly competent for in vitro engineered cartilage formation, which lays a foundation for their potential application in clinical cartilage repair.

摘要

滑膜衍生间充质干细胞(SMSCs)作为一种新型的干细胞,被认为是软骨组织工程的有前途的细胞来源。本研究旨在探讨兔 SMSC 与可注射性凝胶多糖水凝胶联合用于体外工程化软骨。从兔滑膜组织中分离出 SMSC,在单层中扩增至第 4 代,然后包埋在可注射性凝胶多糖水凝胶中,构建体在补充 TGF-β1、TGF-β3 或 BMP-2 的软骨形成培养基中培养长达 42 天。通过 WST-1 测定、实时 RT-PCR、生化分析、组织学和免疫组织化学分析,从细胞增殖和软骨细胞基因/蛋白表达的角度评估构建体的质量。结果表明,TGF-β1、TGF-β3 和 BMP-2 处理的水凝胶中 SMSC 的活力在培养过程中保持较高水平。构建体在培养的第 21 天就形成了软骨组织,表达了软骨细胞基因(Ⅱ型胶原、聚集蛋白聚糖、大软骨素蛋白聚糖、SOX9)和软骨基质(硫酸化糖胺聚糖和胶原)。与 BMP-2 处理的 SMSC 负载水凝胶相比,TGF-β1 和 TGF-β3 处理的 SMSC 负载水凝胶表现出更多的软骨生成。这表明,用 TGF-β1、TGF-β3 或 BMP-2 处理的可注射性 SMSC 负载凝胶在体外构建软骨方面具有很高的能力,为其在临床软骨修复中的潜在应用奠定了基础。

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