Division of Biochemistry, Department of Life science, Hokkaido Pharmaceutical University School of Pharmacy, 7-1 Katsuraoka-cho, Otaru-city, Hokkaido 047-0264, Japan.
J Clin Biochem Nutr. 2009 Nov;45(3):361-9. doi: 10.3164/jcbn.09-47. Epub 2009 Oct 28.
Many researchers have hypothesized that differences in reactive oxygen species levels can trigger the cellular decision between hypertrophy and cell death in cardiomyocytes. In the present study, we examined the relationship between reactive oxygen species levels and hypertrophy or cell death in H9c2 cardiomyocytes after the addition of hydrogen peroxide. Following addition of hydrogen peroxide, we observed a slight increase in fluorescence intensity of 2',7'-dichlorofluorescein, a probe of intracellular reactive oxygen species, and cell hypertrophy in H9c2 cells (normal cells). In contrast, a dramatic increase in fluorescence intensity was followed by cell death in glutathione-depleted H9c2 cells. In the presence of the antioxidant Trolox or the iron chelator deferoxamine, both normal and glutathione-depleted cells developed hypertrophy without a concomitant increase in levels of reactive oxygen species. An inhibitor of p53, pifithrin-alpha, prevented cell death after the addition of hydrogen peroxide; instead a substantial increase in levels of reactive oxygen species and hypertrophy were observed. These results suggest that H9c2 cells exhibit differential sensitivity to intracellular reactive oxygen species generation with regard to their hypertrophic versus death responses to exogenously added hydrogen peroxide.
许多研究人员假设,活性氧水平的差异可以触发心肌细胞中肥大和细胞死亡之间的细胞决策。在本研究中,我们研究了在加入过氧化氢后,H9c2 心肌细胞中活性氧水平与肥大或细胞死亡之间的关系。加入过氧化氢后,我们观察到 2',7'-二氯荧光素(一种细胞内活性氧探针)的荧光强度略有增加,H9c2 细胞(正常细胞)发生了细胞肥大。相比之下,谷胱甘肽耗尽的 H9c2 细胞中荧光强度急剧增加,随后发生细胞死亡。在抗氧化剂 Trolox 或铁螯合剂去铁胺存在的情况下,正常和谷胱甘肽耗尽的细胞均发生肥大,而活性氧水平没有相应增加。p53 抑制剂 pifithrin-alpha 可防止过氧化氢加入后发生细胞死亡;相反,观察到活性氧水平的显著增加和肥大。这些结果表明,H9c2 细胞对细胞内活性氧产生的敏感性存在差异,对于外源性加入的过氧化氢,它们的肥大与死亡反应不同。