Specific toxicity of tunicamycin in induction of programmed cell death of sympathetic neurons

被引:40
作者
Chang, JY
Korolev, VV
机构
[1] Department of Anatomy, Univ. of Arkansas for Med. Sciences, Little Rock
[2] Department of Anatomy, Univ. of Arkansas for Med. Sciences, Little Rock, AR 72205, Slot 510
关键词
D O I
10.1006/exnr.1996.0019
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Tunicamycin belongs to a group of antibiotics which can cause severe and often fatal neurological malfunction in animals, commonly known as ''annual ryegrass toxicity.'' At the cellular level, tunicamycin is a potent glycosylation inhibitor which is often used to elucidate the importance of glycosylation in protein functions. Earlier reports suggested that tunicamycin was able to interfere with the binding of nerve growth factor to its receptors. In this report, we showed that tunicamycin was able to kill sympathetic neurons in cultures. The mechanism of cell death was observed to be similar to that of ''programmed cell death'' in sympathetic neurons induced by nerve growth factor deprivation. Such tunicamycin-induced cell death could be prevented by the protein synthesis inhibitor cycloheximide, which was known to prevent the programmed cell death in sympathetic neurons. These results demonstrated that, in addition to the proven CNS neurotoxicity in animals, tunicamycin causes programmed cell death in peripheral (sympathetic) neurons. (C) 1996 Academic Press, Inc.
引用
收藏
页码:201 / 211
页数:11
相关论文
共 37 条
[1]   ANALYSIS OF EFFECTS OF ANTISERUM TO NERVE GROWTH FACTOR IN ADULT MICE [J].
ANGELETTI, PU ;
LEVIMONT.R ;
CARAMIA, F .
BRAIN RESEARCH, 1971, 27 (02) :343-+
[2]   ZONE MAPPING OF THE BINDING DOMAIN OF THE RAT LOW-AFFINITY NERVE GROWTH-FACTOR RECEPTOR BY THE INTRODUCTION OF NOVEL N-GLYCOSYLATION SITES [J].
BALDWIN, AN ;
SHOOTER, EM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (09) :4594-4602
[3]   EFFECTS OF TUNICAMYCIN ON NGF BINDING AND NEURITE OUTGROWTH IN PC12 CELLS [J].
BARIBAULT, TJ ;
NEET, KE .
JOURNAL OF NEUROSCIENCE RESEARCH, 1985, 14 (01) :49-60
[4]   EXPERIMENTAL TUNICAMYCIN TOXICITY IN CATTLE, SHEEP AND PIGS [J].
BOURKE, CA ;
CARRIGAN, MJ .
AUSTRALIAN VETERINARY JOURNAL, 1993, 70 (05) :188-189
[5]   INTERFERON SUPPRESSES SYMPATHETIC NEURONAL CELL-DEATH CAUSED BY NERVE GROWTH-FACTOR DEPRIVATION [J].
CHANG, JY ;
MARTIN, DP ;
JOHNSON, EM .
JOURNAL OF NEUROCHEMISTRY, 1990, 55 (02) :436-445
[6]   TEMPORAL ANALYSIS OF EVENTS ASSOCIATED WITH PROGRAMMED CELL-DEATH (APOPTOSIS) OF SYMPATHETIC NEURONS DEPRIVED OF NERVE GROWTH-FACTOR [J].
DECKWERTH, TL ;
JOHNSON, EM .
JOURNAL OF CELL BIOLOGY, 1993, 123 (05) :1207-1222
[7]   INHIBITION OF PROTEIN GLYCOSYLATION AND SELECTIVE CYTO-TOXICITY TOWARD VIRALLY TRANSFORMED FIBROBLASTS CAUSED BY B3-TUNICAMYCIN [J].
DUKSIN, D ;
SEIBERG, M ;
MAHONEY, WC .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1982, 129 (01) :77-80
[8]   CHARACTERIZATION OF APOPTOSIS IN CULTURED RAT SYMPATHETIC NEURONS AFTER NERVE GROWTH-FACTOR WITHDRAWAL [J].
EDWARDS, SN ;
TOLKOVSKY, AM .
JOURNAL OF CELL BIOLOGY, 1994, 124 (04) :537-546
[9]   THE DEATH PROGRAM IN CULTURED SYMPATHETIC NEURONS CAN BE SUPPRESSED AT THE POSTTRANSLATIONAL LEVEL BY NERVE GROWTH-FACTOR, CYCLIC-AMP, AND DEPOLARIZATION [J].
EDWARDS, SN ;
BUCKMASTER, AE ;
TOLKOVSKY, AM .
JOURNAL OF NEUROCHEMISTRY, 1991, 57 (06) :2140-2143