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293 Cell Cycle Synchronisation In Adenovirus Vector Production

机译:腺病毒载体生产中的293细胞周期同步

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As the market requirements for adenovirus vectors(AdV)increase,the maximisation of the virus titer per culture volume per unit time is a key requirement.However,despite the fact that 293 cells can grow up to 8 X 10 celllmL in simple batch mode operations,for optimal AdV infection a maximum cell density of 1 X 10 celllmL at infection time has usually been utilized due to the so called"cell density effect".In addition,AdV titer appears to be dependent upon cell cycle phase at the time of infection.To evaluate the dependence of AdV production upon cell cycle phase,293 cells were chemically synchronised at each phase of the cell cycle;a 2.6-fold increase on AdV cell specific titer was obtained when the percentage of cells at the S phase of the cell cycle was increased from 36 to 47%;a mathematical equation was used to relate AdV cell specific productivities with cell synchronisation at the S phase using this data.To avoid the use of chemical inhibitors,a temperature shift strategy was also used for synchronisation at the S phase.S phase synchronisation was obtained by decreasing the culture temperature to 31°C during 67 h and restoring it to 37°C during 72 h.By using this strategy we were able to synchronise 57% of the population in the S phase of the cell cycle obtaining an increase of 7.3-fold on AdV cell specific titer after infection.
机译:随着腺病毒载体(AdV)市场需求的增加,最大化每单位时间每培养量的病毒滴度是一个关键要求。但是,尽管在简单的批处理模式下293细胞可以增长到8 X 10细胞/ mL。对于最佳的AdV感染,由于所谓的“细胞密度效应”,通常在感染时使用的最大细胞密度为1 X 10细胞毫升。此外,AdV滴度似乎取决于感染时的细胞周期阶段。为了评估AdV产生对细胞周期阶段的依赖性,在细胞周期的每个阶段对293细胞进行了化学同步处理;当细胞处于S期时,AdV细胞的特异性滴度增加了2.6倍周期从36%增加到47%;使用此数据,使用数学方程式将AdV细胞的特定生产率与S期细胞同步相关。为避免使用化学抑制剂,还采用了温度转换策略通过在67小时内将培养温度降低到31°C并在72小时内恢复到37°C来实现S期同步。通过这种策略,我们可以同步57%的种群在细胞周期的S期,感染后AdV细胞特异性滴度增加7.3倍。

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