A CELLULAR-MODEL OF OXIDANT-MEDIATED NEURONAL INJURY

被引:59
作者
HINSHAW, DB
MILLER, MT
OMANN, GM
BEALS, TF
HYSLOP, PA
机构
[1] VET ADM MED CTR, DEPT BIOL CHEM, ANN ARBOR, MI 48105 USA
[2] UNIV MICHIGAN, ANN ARBOR, MI 48109 USA
[3] VET ADM MED CTR, DEPT PATHOL, ANN ARBOR, MI 48105 USA
[4] ELI LILLY & CO, LILLY RES LAB, DIV CNS, INDIANAPOLIS, IN 46285 USA
关键词
PC; 12; CELL; CELL INJURY; HYDROGEN PEROXIDE; MICROTUBULE; MICROFILAMENT; CELL CALCIUM;
D O I
10.1016/0006-8993(93)91110-E
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Oxidants derived from the partial reduction of oxygen are thought to play a significant role in neuronal injury. We present here a cellular model of neuronal injury mediated by hydrogen peroxide (H2O2) using the PC 12 rat pheochromocytoma cell line. The organization of microtubules and microfilaments within neurites of PC 12 cells differentiated by exposure to nerve growth factor was examined after H2O2 injury using fluorescence microscopy. Concentrations of H2O2 as low as 100 muM produced an initial periodic pattern of microtubule depolymerization over 3-4 h which later progressed to complete depolymerization. Neuritic microspikes containing actin filaments were relatively more resistant to injury by H2O2 than microtubules. Blebbing of PC 12 cell bodies and neurites also was seen after H2O2 injury and the blebs appeared to contain microtubules. The destructive changes affecting neuritic structure preceded but were not essential for PC 12 cell lysis. Exposure of the cells to the Ca2+ ionophore, ionomycin (25 muM) also produced the same pattern of microtubule depolymerization in PC 12 neurites as was seen after H2O2 injury suggesting that H2O2 may mediate its destructive effect on the neurites via elevation of intracellular Ca2+.
引用
收藏
页码:13 / 26
页数:14
相关论文
共 31 条
[1]  
BLACK MM, 1987, J NEUROSCI, V7, P1833
[2]   CENTRAL NERVOUS-SYSTEM TRAUMA AND STROKE .1. BIOCHEMICAL CONSIDERATIONS FOR OXYGEN RADICAL FORMATION AND LIPID-PEROXIDATION [J].
BRAUGHLER, JM ;
HALL, ED .
FREE RADICAL BIOLOGY AND MEDICINE, 1989, 6 (03) :289-301
[3]   POSTTRANSLATIONAL MODIFICATIONS OF ALPHA-TUBULIN - ACETYLATED AND DETYROSINATED FORMS IN AXONS OF RAT CEREBELLUM [J].
CAMBRAYDEAKIN, MA ;
BURGOYNE, RD .
JOURNAL OF CELL BIOLOGY, 1987, 104 (06) :1569-1574
[4]  
CAMBRAYDEAKIN MA, 1991, CYTOSKELETON GROWING, P233
[5]   ESTABLISHMENT OF A NORADRENERGIC CLONAL LINE OF RAT ADRENAL PHEOCHROMOCYTOMA CELLS WHICH RESPOND TO NERVE GROWTH-FACTOR [J].
GREENE, LA ;
TISCHLER, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1976, 73 (07) :2424-2428
[6]   CENTRAL NERVOUS-SYSTEM TRAUMA AND STROKE .2. PHYSIOLOGICAL AND PHARMACOLOGICAL EVIDENCE FOR INVOLVEMENT OF OXYGEN RADICALS AND LIPID-PEROXIDATION [J].
HALL, ED ;
BRAUGHLER, JM .
FREE RADICAL BIOLOGY AND MEDICINE, 1989, 6 (03) :303-313
[7]   REVERSIBLE AND IRREVERSIBLE OXIDANT INJURY TO PC12 CELLS BY HYDROGEN-PEROXIDE [J].
HALLECK, MM ;
RICHBURG, JH ;
KAUFFMAN, FC .
FREE RADICAL BIOLOGY AND MEDICINE, 1992, 12 (02) :137-144
[8]   OXIDANTS AND THE CENTRAL-NERVOUS-SYSTEM - SOME FUNDAMENTAL QUESTIONS - IS OXIDANT DAMAGE RELEVANT TO PARKINSONS-DISEASE, ALZHEIMERS-DISEASE, TRAUMATIC INJURY OR STROKE [J].
HALLIWELL, B .
ACTA NEUROLOGICA SCANDINAVICA, 1989, 80 :23-33
[9]  
HINSHAW DB, 1986, AM J PATHOL, V123, P454
[10]   MECHANISM OF ENDOTHELIAL-CELL SHAPE CHANGE IN OXIDANT INJURY [J].
HINSHAW, DB ;
BURGER, JM ;
ARMSTRONG, BC ;
HYSLOP, PA .
JOURNAL OF SURGICAL RESEARCH, 1989, 46 (04) :339-349