Changes in mitochondrial membrane potential during oxidative stress-induced apoptosis in PC12 cells

被引:0
作者
Satoh, T
Enokido, Y
Aoshima, H
Uchiyama, Y
Hatanaka, H
机构
[1] OSAKA UNIV,INST PROT RES,DIV PROT BIOSYNTH,SUITA,OSAKA 565,JAPAN
[2] YAMAGUCHI UNIV,FAC LIBERAL ARTS,DEPT CHEM,YAMAGUCHI,JAPAN
[3] OSAKA UNIV,SCH MED,DEPT ANAT,OSAKA,JAPAN
关键词
oxidative stress; apoptosis; mitochondria; BCL-2; reactive oxygen species;
D O I
10.1002/(SICI)1097-4547(19971101)50:3<413::AID-JNR7>3.0.CO;2-L
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We examined the effects of various types of oxidative stress on cell survival and on mitochondrial membrane potential (Delta Psi m) in PC12 cells transfected with BCL-2, Several types of oxidative stress such as exposure to hydrogen peroxide, 13-L-hydroperoxylinoleic acid, and xanthine + xanthine oxidase triggered apoptotic nuclear condensation and DNA fragmentation in normal PC12 cells, These types of oxidative stress induced significant increases in level of reactive oxygen species (ROS) before cell death, By contrast, BCL-2 prevented the apoptosis induced by these oxidative stresses, However, BCL-2 did not reduce ROS levels, indicating that it functions downstream of ROS generation, We measured Delta Psi m as a potential target of ROS during oxidative stress-induced cell death, Hydrogen peroxide, 13-L-hydroperoxylinoleic acid, and xanthine + xanthine oxidase induced a significant loss of Delta Psi m simultaneously with cell death, BCL-2 prevented the decrease in Delta Psi m as well as apoptosis induced by oxidative stress, These observations suggest that the oxidative stress triggers apoptosis associated with both increased generation of ROS and decreases in level of Delta Psi m and that BCL-2 prevents cell death as well as Delta Psi m but not ROS production. (C) 1997 Wiley-Liss, Inc.
引用
收藏
页码:413 / 420
页数:8
相关论文
共 46 条
[1]   THE PROTOONCOGENE BCL-2 CAN SELECTIVELY RESCUE NEUROTROPHIC FACTOR-DEPENDENT NEURONS FROM APOPTOSIS [J].
ALLSOPP, TE ;
WYATT, S ;
PATERSON, HF ;
DAVIES, AM .
CELL, 1993, 73 (02) :295-307
[2]   GLUTAMATE-INDUCED NEURONAL DEATH - A SUCCESSION OF NECROSIS OR APOPTOSIS DEPENDING ON MITOCHONDRIAL-FUNCTION [J].
ANKARCRONA, M ;
DYPBUKT, JM ;
BONFOCO, E ;
ZHIVOTOVSKY, B ;
ORRENIUS, S ;
LIPTON, SA ;
NICOTERA, P .
NEURON, 1995, 15 (04) :961-973
[3]   Generation of free radicals during lipid hydroperoxide-triggered apoptosis in PC12h cells [J].
Aoshima, H ;
Satoh, T ;
Sakai, N ;
Yamada, M ;
Enokido, Y ;
Ikeuchi, T ;
Hatanaka, H .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1997, 1345 (01) :35-42
[4]   DOES IMPAIRMENT OF ENERGY-METABOLISM RESULT IN EXCITOTOXIC NEURONAL DEATH IN NEURODEGENERATIVE ILLNESSES [J].
BEAL, MF .
ANNALS OF NEUROLOGY, 1992, 31 (02) :119-130
[5]   HYDROGEN-PEROXIDE MEDIATES AMYLOID-BETA PROTEIN TOXICITY [J].
BEHL, C ;
DAVIS, JB ;
LESLEY, R ;
SCHUBERT, D .
CELL, 1994, 77 (06) :817-827
[6]   MITOCHONDRIAL MODIFICATIONS DURING RAT THYMOCYTE APOPTOSIS - A STUDY AT THE SINGLE-CELL LEVEL [J].
COSSARIZZA, A ;
KALASHNIKOVA, G ;
GRASSILLI, E ;
CHIAPPELLI, F ;
SALVIOLI, S ;
CAPRI, M ;
BARBIERI, D ;
TROIANO, L ;
MONTI, D ;
FRANCESCHI, C .
EXPERIMENTAL CELL RESEARCH, 1994, 214 (01) :323-330
[7]  
DUGAN LL, 1995, J NEUROSCI, V15, P6377
[8]   HIGH OXYGEN ATMOSPHERE FOR NEURONAL CELL-CULTURE WITH NERVE GROWTH-FACTOR .2. SURVIVAL AND GROWTH OF CLONAL RAT PHEOCHROMOCYTOMA PC12H CELLS [J].
ENOKIDO, Y ;
HATANAKA, H .
BRAIN RESEARCH, 1990, 536 (1-2) :23-29
[9]   APOPTOTIC CELL-DEATH OCCURS IN HIPPOCAMPAL-NEURONS CULTURED IN A HIGH OXYGEN ATMOSPHERE [J].
ENOKIDO, Y ;
HATANAKA, H .
NEUROSCIENCE, 1993, 57 (04) :965-972
[10]   BASIC FIBROBLAST GROWTH-FACTOR RESCUES CNS NEURONS FROM CELL-DEATH CAUSED BY HIGH OXYGEN ATMOSPHERE IN CULTURE [J].
ENOKIDO, Y ;
AKANEYA, Y ;
NIINOBE, M ;
MIKOSHIBA, K ;
HATANAKA, H .
BRAIN RESEARCH, 1992, 599 (02) :261-271