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Reactive oxygen species are related to ionic fluxes and volume decrease in apoptotic cerebellar granule neurons: role of NOX enzymes
被引:11
作者:
Hernandez-Enriquez, Berenice
[1
]
Guemez-Gamboa, Alicia
[1
]
Moran, Julio
[1
]
机构:
[1] Univ Nacl Autonoma Mexico, Div Neurociencias, Inst Fisiol Celular, Dept Neurodesarrollo & Fisiol, Mexico City 04510, DF, Mexico
关键词:
apoptosis;
apoptotic volume decrease;
ionic fluxes;
NADPH oxidase;
potassium deprivation;
staurosporine;
NIH3T3 MOUSE FIBROBLASTS;
NADPH OXIDASE ACTIVATION;
OXIDATIVE STRESS;
CELL-DEATH;
POTASSIUM DEPRIVATION;
CHLORIDE CHANNELS;
NAD(P)H OXIDASE;
TAURINE EFFLUX;
MUSCLE CELLS;
DEPOLARIZATION;
D O I:
10.1111/j.1471-4159.2011.07231.x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
P>Reactive oxygen species (ROS) are produced early during apoptosis of cerebellar granule neurons induced by low potassium (K5) and staurosporine (Sts). In addition, K5 and Sts activate NADPH oxidases (NOX). Recently, we described that K5 and Sts induce apoptotic volume decrease (AVD) at a time when ROS generation and NOX activity occur. In the present study, we evaluated the relationship between ROS generation and ionic fluxes during AVD. Here, we showed that K5- and Sts-induced AVD was inhibited by antioxidants and that direct ROS production induced AVD. Moreover, NOX inhibitors eliminated AVD induced by both K5 and Sts. Sts, but not K5, failed to induce AVD in cerebellar granule neurons from NOX2 knockout mice. These findings suggest that K5- and Sts-induced AVD is largely mediated by ROS produced by NOX. On the other hand, we also found that the blockage of ionic fluxes involved in AVD inhibited both ROS generation and NOX activity. These findings suggest that ROS generation and NOX activity are involved in ionic fluxes activation, which in turn could maintain ROS generation by activating NOX, leading to a self-amplifying cycle.
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页码:654 / 664
页数:11
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