Chen H-C, Sung L-Y, Lo W-H, Chuang C-K, Wang Y-H, Lin J-L, Hu Y-C
Department of Chemical Engineering, National Tsing Hua University, Hsinchu, Taiwan.
Gene Ther. 2008 Feb;15(4):309-17. doi: 10.1038/sj.gt.3303087. Epub 2007 Dec 6.
Baculovirus is an emerging gene delivery vector, thanks to a number of unique advantages. Herein, we genetically modified the rabbit articular chondrocytes with a recombinant baculovirus (Bac-CB) encoding bone morphogenetic protein-2 (BMP-2), which conferred high level BMP-2 expression and triggered the re-differentiation of dedifferentiated third passage (P3) chondrocytes in the monolayer culture. The transduced and mock-transduced P3 cells were seeded into porous scaffolds and cultured in either the dishes or the rotating-shaft bioreactor (RSB), a novel bioreactor imparting a dynamic, two-phase culture environment. Neither mock-transduced constructs in the RSB culture nor the Bac-CB-transduced constructs in the static culture grew into uniform cartilaginous tissues. Only the Bac-CB-transduced constructs cultured in the RSB for 3 weeks resulted in cartilaginous tissues with hyaline appearance, uniform cell distribution, cartilage-specific gene expression and considerably enhanced cartilage-specific extracellular matrix deposition, as determined by histological staining, reverse transcription-PCR analyses and biochemical assays. This is the first study demonstrating that combination of baculovirus-mediated growth factor expression and RSB culture synergistically enhanced in vitro creation of cartilaginous tissues from dedifferentiated chondrocytes. Since baculovirus transduction is generally considered safe, this approach represents a viable alternative to stimulate the formation of engineered cartilage in a more cost-effective way than the growth factor supplementation.
杆状病毒由于具有许多独特优势,正成为一种新兴的基因传递载体。在此,我们用编码骨形态发生蛋白-2(BMP-2)的重组杆状病毒(Bac-CB)对兔关节软骨细胞进行基因改造,该病毒使BMP-2实现高水平表达,并触发了单层培养中去分化的第三代(P3)软骨细胞的再分化。将转导和未转导的P3细胞接种到多孔支架中,并在培养皿或旋转轴生物反应器(RSB)中培养,RSB是一种能提供动态两相培养环境的新型生物反应器。在RSB培养中的未转导构建体和静态培养中的Bac-CB转导构建体均未生长成均匀的软骨组织。只有在RSB中培养3周的Bac-CB转导构建体产生了外观为透明软骨、细胞分布均匀、具有软骨特异性基因表达且软骨特异性细胞外基质沉积显著增强的软骨组织,这通过组织学染色、逆转录-PCR分析和生化测定得以确定。这是第一项表明杆状病毒介导的生长因子表达与RSB培养相结合能协同增强从去分化软骨细胞体外构建软骨组织的研究。由于杆状病毒转导通常被认为是安全的,这种方法代表了一种可行的替代方案,能以比补充生长因子更具成本效益的方式刺激工程软骨的形成。