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基因修饰去分化软骨细胞与 ATDC5 细胞共培养体系中增强的软骨生成。

Enhanced chondrogenesis in a coculture system with genetically manipulated dedifferentiated chondrocytes and ATDC5 cells.

机构信息

Department of Joint Surgery, The First Affiliated Hospital of Guangzhou Medical University, Guangzhou, China.

Guangdong Key Laboratory of Orthopaedic Technology and Implant Materials, Guangzhou, China.

出版信息

Biotechnol Bioeng. 2020 Oct;117(10):3173-3181. doi: 10.1002/bit.27482. Epub 2020 Jul 14.

Abstract

Articular cartilage repair after injury is a great challenge worldwide due to its nerveless and avascular features. Tissue engineering is proposed as a promising alternative for cartilage regeneration. In this study, an adenoviral vector carrying the transforming growth factor-β3 (TGF-β3) gene was constructed and introduced into dedifferentiated chondrocytes, which were then cocultured with ATDC5 cells in an alginate hydrogel system. The results showed that the experimental groups exhibited better cell viability and higher levels of cartilage-related genes than the control groups. In this coculture system, the chondrogenic differentiation of ATDC5 cells was effectively induced by TGF-β3 and other latent cytokines that were produced by the transfected chondrocytes. Thus, this method can avoid the degradation of exogenous TGF-β3, and it can protect ATDC5 cells during virus transfection to maintain cell viability and chondrogenic differentiation capability. Taken together, this study provides fresh insights for applying this genetically manipulated coculture system to cartilage repair in the future.

摘要

关节软骨损伤后的修复是一个全球性的巨大挑战,因为它具有无神经和无血管的特点。组织工程被提出作为软骨再生的一种有前途的替代方法。在这项研究中,构建了携带转化生长因子-β3(TGF-β3)基因的腺病毒载体,并将其导入去分化软骨细胞中,然后将其与 ATDC5 细胞在藻酸盐水凝胶系统中共培养。结果表明,实验组的细胞活力和软骨相关基因水平均高于对照组。在这种共培养系统中,TGF-β3 和转染软骨细胞产生的其他潜在细胞因子有效诱导了 ATDC5 细胞的软骨分化。因此,这种方法可以避免外源性 TGF-β3 的降解,并可以在病毒转染过程中保护 ATDC5 细胞,维持细胞活力和软骨分化能力。总之,这项研究为将来将这种基因修饰的共培养系统应用于软骨修复提供了新的见解。

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