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通过细胞介导的基因疗法持续分泌转化生长因子β1可维持软骨细胞的再分化。

Continuous transforming growth factor beta1 secretion by cell-mediated gene therapy maintains chondrocyte redifferentiation.

作者信息

Lee Dug Keun, Choi Kyoung Baek, Oh In Suk, Song Sun U, Hwang Sally, Lim Chae-Lyul, Hyun Jong-Pil, Lee Hyeon-Youl, Chi Guang Fan, Yi Youngsuk, Yip Vivian, Kim Jeannie, Lee Eun Byul, Noh Moon Jong, Lee Kwan Hee

机构信息

TissueGene, Gaithersburg, Maryland 20877, USA.

出版信息

Tissue Eng. 2005 Jan-Feb;11(1-2):310-8. doi: 10.1089/ten.2005.11.310.

Abstract

One of the most important factors in the production of cartilage is transforming growth factor beta1 (TGF-beta1). To obtain sustained release of TGF-beta1, a cell-mediated gene therapy technique was introduced. We infected chondrocytes with a retroviral vector carrying the TGF-beta1 gene. The single clone derivative showed sustained TGF-beta1 secretion. It also showed constitutive type II collagen expression. Whereas the TGF-beta1 protein itself is unable to induce formation of cartilage in vivo, human chondrocytes engineered to express a retroviral vector encoding TGF-beta1 showed cartilage formation in vivo when cells were injected into nude mice intradermally. These data suggest that cell-mediated gene therapy using TGF-beta1 as a transgene would be a promising treatment for osteoarthritis.

摘要

软骨生成过程中最重要的因素之一是转化生长因子β1(TGF-β1)。为实现TGF-β1的持续释放,引入了一种细胞介导的基因治疗技术。我们用携带TGF-β1基因的逆转录病毒载体感染软骨细胞。单克隆衍生物表现出TGF-β1的持续分泌。它还表现出组成型II型胶原蛋白表达。虽然TGF-β1蛋白本身无法在体内诱导软骨形成,但当将经基因工程改造以表达编码TGF-β1的逆转录病毒载体的人软骨细胞皮内注射到裸鼠体内时,可在体内形成软骨。这些数据表明,以TGF-β1作为转基因的细胞介导基因治疗可能是骨关节炎的一种有前景的治疗方法。

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