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Effects of temperature shift on cell cycle, apoptosis and nucleotide pools in CHO cell batch cultues

机译:温度变化对CHO细胞分批培养细胞周期,凋亡和核苷酸库的影响

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Temperature reduction in CHO cell batch culture may be beneficial in the production of recombinant protein and in maintenance of viability. The effects on cell cycle, apoptosis and nucleotide pools were studied in cultures initiated at 37°C and temperature shifted to 30 °C after 48 hours. In control cultures maintained at 37 °C, viable cells continued to proliferate until the termination of the culture, however, temperature reduction caused a rapid decrease in the percent of cells in S phase and accumulation of cells in G-1. This was accompanied by a concurrent reduction in U ratio (UTO/UDP-GNAc), previously shown to be a sensitive indicator of growth rate. Culture viability was extended following temperature shift, as a result of delayed onset of apoptosis, however, once initiated, the rate and manner of cell death was similar to that observed at 37 °C. All nucleotide pools were similarly degraded at the time of apoptotic cell death. Temperature reduction to 30 °C did not decrease the energy charge of the cells, however, the overall rate of metabolism was reduced. The latter may be sufficient to extend culture viability via a reduction in toxic metabolites and/or limitation of nutrient deprivation. However, the possibility remains that the benefits of temperature reduction in terms of both viability and productivity are more directly associated with cultures spending extended time in G-1.
机译:CHO细胞分批培养中的温度降低可能对重组蛋白的生产和维持活力有益。在37°C起始的培养物中研究了对细胞周期,凋亡和核苷酸库的影响,温度在48小时后移至30°C。在保持在37°C的对照培养物中,活细胞继续增殖直至培养终止,但是,温度降低导致S期细胞百分比迅速下降,而G-1细胞却蓄积。同时伴随着U比值的降低(UTO / UDP-GNAc),以前被证明是增长率的敏感指标。由于细胞凋亡的延迟发作,温度变化后培养力得以延长,但是一旦启动,细胞死亡的速率和方式与在37°C下观察到的相似。在凋亡细胞死亡时,所有核苷酸库均类似地降解。将温度降低至30°C并不会减少细胞的能量电荷,但是新陈代谢的整体速率却降低了。后者可能足以通过减少毒性代谢产物和/或限制营养剥夺来延长培养力。然而,可能性仍然存在,温度降低在生存力和生产率方面的好处与文化在G-1上花费更长的时间直接相关。

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