Ferreira T B, Carrondo M J T, Alves P M
Instituto de Biologia Experimental e Tecnológica, Apartado 12, P-2781-901 Oeiras, Portugal.
J Biotechnol. 2007 May 1;129(3):433-8. doi: 10.1016/j.jbiotec.2007.01.010. Epub 2007 Jan 23.
Recombinant adenoviral vectors (AdV) have proven to be highly efficient for the delivery and expression of foreign genes in a broad spectrum of cell types and species both for vaccination and gene therapy in a number of specific applications. In this study, the effect of ammonia production on intracellular pH (pH(i)) and consequently inhibition of AdV production at high cell densities is assessed. Different specific ammonia production rates were obtained for 293 cells adapted to grow in glutamate supplemented medium (non-ammoniagenic medium) as compared with 293 cells growing in glutamine supplemented medium (ammoniagenic medium); pH(i) was observed to be lower during cell growth and AdV production at both high and low CCI in the ammoniagenic medium, where the specific ammonia production rate is higher. In addition, after infection at CCI of 3x10(6)cell/ml, the cell viability decreased significantly in the ammoniagenic medium, attributed to the activation of an acidic pathway of apoptosis. Furthermore, AdV DNA was observed to be degraded at the observed pH(i) in the ammoniagenic medium, decreasing significantly the amount of AdV DNA available for encapsulation. To elucidate the pH(i) effect upon AdV production, 293 cells were infected at a CCI of 1 x 10(6)cell/ml in the non-ammoniagenic medium with a manipulated pH(i) as observed at the time of infection at CCI of 3 x 10(6)cell/ml in the ammoniagenic (pH(i) 7.0) and non-ammoniagenic (pH(i) 7.3) media; AdV volumetric productivities were observed to be lower when the cells were exposed to the lower pH(i). Thus, the importance of controlling all the factors contributing to pH(i) on AdV production, such as ammonia production, has been established.
重组腺病毒载体(AdV)已被证明在多种细胞类型和物种中,对于疫苗接种和许多特定应用中的基因治疗而言,在递送和表达外源基因方面具有高效性。在本研究中,评估了氨生成对细胞内pH值(pH(i))的影响以及因此在高细胞密度下对AdV生产的抑制作用。与在补充谷氨酰胺的培养基(产氨培养基)中生长的293细胞相比,适应于在补充谷氨酸的培养基(非产氨培养基)中生长的293细胞获得了不同的特定氨生成速率;在产氨培养基中,特定氨生成速率较高,在高和低细胞浓度指数(CCI)下细胞生长和AdV生产期间观察到pH(i)较低。此外,在3x10(6)细胞/ml的CCI感染后,产氨培养基中的细胞活力显著下降,这归因于凋亡酸性途径的激活。此外,在产氨培养基中观察到的pH(i)下AdV DNA会降解,显著减少了可用于包装的AdV DNA量。为了阐明pH(i)对AdV生产的影响,在非产氨培养基中以1 x 10(6)细胞/ml的CCI感染293细胞,其pH(i)如在产氨(pH(i) 7.0)和非产氨(pH(i) 7.3)培养基中3 x 10(6)细胞/ml的CCI感染时所观察到的那样进行调控;当细胞暴露于较低的pH(i)时,观察到AdV体积生产率较低。因此,已经确定了控制所有影响pH(i)的因素(如氨生成)对AdV生产的重要性。