Lin A A, Miller W M
Department of Chemical Engineering, Northwestern University, Evanston, Illinois 60208-3120, USA.
Biotechnol Bioeng. 1992 Aug 5;40(4):505-16. doi: 10.1002/bit.260400409.
We have investigated the regulation of oxygen consumption and modulation of glutathione levels in CHO-K1 cells under oxygen-limiting conditions. We report here suppression of oxygen consumption and alteration of the supply-dependent relationship as a consequence of prolonged hypoxic or anoxic exposure. The suppression is characterized by an increase in the value of P(o(2)/50) (the oxygen tension at which oxygen consumption is half maximal). Under prolonged anoxia there is also a decrease in the cells' potential to use oxygen. Elevated glucose consumption under low oxygen conditions may contribute to the suppression in respiration. The glutathione concentration remains constant throughout hypoxic exposure but may decrease by as much as 40% under anoxia. The glutathione level in hypoxic and anoxic cells increases by two- and four-fold, respectively, over that of the control cells when exposed to a cytotoxic level of oxygen (93%). This suggests that anoxic and hypoxic exposure sensitizes CHO cells to oxidative stress.
我们研究了在氧限制条件下CHO-K1细胞中氧消耗的调节以及谷胱甘肽水平的调控。我们在此报告,长时间的缺氧或无氧暴露会导致氧消耗受到抑制以及供应依赖关系发生改变。这种抑制的特征是P(o(2)/50)(氧消耗达到最大值一半时的氧张力)值增加。在长时间的无氧状态下,细胞利用氧的能力也会下降。低氧条件下葡萄糖消耗的增加可能导致呼吸抑制。在整个缺氧暴露过程中,谷胱甘肽浓度保持恒定,但在无氧状态下可能会降低多达40%。当暴露于细胞毒性水平的氧(93%)时,缺氧和无氧细胞中的谷胱甘肽水平分别比对照细胞增加了两倍和四倍。这表明缺氧和无氧暴露会使CHO细胞对氧化应激敏感。