Hackenbrock C R, Rehn T G, Weinbach E C, Lemasters J J
J Cell Biol. 1971 Oct;51(1):123-37. doi: 10.1083/jcb.51.1.123.
We have examined the ultrastructure of mitochondria as it relates to energy metabolism in the intact cell. Oxidative phosphorylation was induced in ultrastructurally intact Ehrlich ascites tumor cells by rapidly generating intracellular adenosine diphosphate from endogenous adenosine triphosphate by the addition of 2-deoxyglucose. The occurrence of oxidative phosphorylation was ascertained indirectly by continuous and synchronous monitoring of respiratory rate, fluorescence of pyridine nucleotide, and 90 degrees light-scattering. Oxidative phosphorylation was confirmed by direct enzymatic analysis of intracellular adenine nucleotides and by determination of intracellular inorganic orthophosphate. Microsamples of cells rapidly fixed for electron microscopy revealed that, in addition to oxidative phosphorylation, an orthodox --> condensed ultrastructural transformation occurred in the mitochondria of all cells in less than 6 sec after the generation of adenosine diphosphate by 2-deoxyglucose. A 90 degrees light-scattering increase, which also occurs at this time, showed a t (1/2) of only 25 sec which agreed temporally with a slower orthodox --> maximally condensed mitochondrial transformation. Neither oxidative phosphorylation nor ultrastructural transformation could be initiated in mitochondria in intact cells by the intracellular generation of adenosine diphosphate in the presence of uncouplers of oxidative phosphorylation. Partial and complete inhibition of oxidative phosphorylation by oligomycin resulted in a positive relationship to partial and complete inhibition of 2-deoxyglucose-induced ultrastructural transformation in the mitochondria in these cells. The data presented reveal that an orthodox --> condensed ultrastructural transformation is linked to induced oxidative phosphorylation in mitochondria in the intact ascites tumor cell.
我们研究了线粒体的超微结构,及其与完整细胞能量代谢的关系。通过添加2-脱氧葡萄糖,使内源性三磷酸腺苷快速生成细胞内二磷酸腺苷,从而在超微结构完整的艾氏腹水瘤细胞中诱导氧化磷酸化。通过连续同步监测呼吸速率、吡啶核苷酸荧光和90度光散射间接确定氧化磷酸化的发生。通过对细胞内腺嘌呤核苷酸的直接酶分析和细胞内无机磷酸的测定来确认氧化磷酸化。快速固定用于电子显微镜观察的细胞微量样品显示,除了氧化磷酸化外,在2-脱氧葡萄糖生成二磷酸腺苷后不到6秒内,所有细胞的线粒体中都发生了从正统型到浓缩型的超微结构转变。此时也出现的90度光散射增加,其半衰期仅为25秒,在时间上与较慢的从正统型到最大浓缩型的线粒体转变一致。在氧化磷酸化解偶联剂存在的情况下,通过细胞内生成二磷酸腺苷,完整细胞中的线粒体无法启动氧化磷酸化或超微结构转变。寡霉素对氧化磷酸化的部分和完全抑制,与这些细胞中线粒体中2-脱氧葡萄糖诱导的超微结构转变的部分和完全抑制呈正相关。所呈现的数据表明,从正统型到浓缩型的超微结构转变与完整腹水瘤细胞中线粒体诱导的氧化磷酸化有关。