Hao Jinghua, Yao Yongchang, Varshney Rohan R, Wang Laicheng, Prakash Celine, Li Hao, Wang Dong-An
Division of Bioengineering, School of Chemical and Biomedical Engineering, Nanyang Technological University , Singapore, Republic of Singapore.
Tissue Eng Part C Methods. 2008 Dec;14(4):273-80. doi: 10.1089/ten.tec.2008.0163.
Cartilage restoration continues to present a tremendous clinical challenge due to its nonvascular nature. Many studies have demonstrated that chondrogenesis of progenitor cells can be achieved in vitro by manual dose of growth factors; however, it remains a vital difficulty in feeding growth factors to implanted therapeutic cells in vivo. Herein, we constructed recombinant adenovirus encoding human transforming growth factor-beta3 (hTGF-beta3) and practiced it in rat bone marrow-derived mesenchymal stromal cells and articular chondrocytes for cartilage regeneration. Optimal viable transduction and transgenic hTGF-beta3 production were achieved; consequently, positive expression of cartilage marker-collagen type II was enabled in the infected progenitors. We thus conclude that recombinant adenovirus encoding TGF-beta3 gene has been successfully established and validated for cartilage tissue engineering applications.
由于软骨的无血管特性,软骨修复仍然是一个巨大的临床挑战。许多研究表明,通过手动给予生长因子,祖细胞的软骨形成可以在体外实现;然而,在体内向植入的治疗性细胞输送生长因子仍然是一个至关重要的难题。在此,我们构建了编码人转化生长因子-β3(hTGF-β3)的重组腺病毒,并将其应用于大鼠骨髓间充质基质细胞和关节软骨细胞以进行软骨再生。实现了最佳的存活转导和转基因hTGF-β3的产生;因此,在受感染的祖细胞中实现了软骨标志物II型胶原蛋白的阳性表达。我们由此得出结论,编码TGF-β3基因的重组腺病毒已成功构建并验证可用于软骨组织工程应用。