HEME OXYGENASE IS A HEAT-SHOCK PROTEIN AND PEST PROTEIN IN RAT ASTROGLIAL CELLS

被引:83
作者
DWYER, BE
NISHIMURA, RN
DEVELLIS, J
YOSHIDA, T
机构
[1] VET AFFAIRS MED CTR,INVITRO REMYELINAT LAB,SEPULVEDA,CA 91343
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT NEUROL,LOS ANGELES,CA 90024
[3] UNIV CALIF LOS ANGELES,SCH MED,DEPT ANAT & PSYCHIAT,LOS ANGELES,CA 90024
[4] UNIV CALIF LOS ANGELES,SCH MED,BRAIN RES INST,LOS ANGELES,CA 90024
[5] UNIV CALIF LOS ANGELES,SCH MED,MENTAL RETARDAT RES CTR,LOS ANGELES,CA 90024
[6] YAMAGATA UNIV,SCH MED,DEPT MOLEC & PATHOL BIOCHEM,YAMAGATA 990,JAPAN
关键词
STRESS PROTEIN; CANCER; BRAIN; OXIDATIVE INJURY;
D O I
10.1002/glia.440050407
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Cultured rat forebrain astrocytes contained significant amounts of immunostainable heme oxygenase-1 (HO-1) isozyme, whereas HO-1 was undetectable in spontaneously transformed rat astroglial cells (ATs). HO-1 was inducible in both cell types by heat shock and by submicromolar amounts of H2O2. Inhibition of RNA synthesis with actinomycin D or protein synthesis with cycloheximide resulted in the rapid loss of immunostainable heme oxygenase in astrocytes. Analysis of the primary structure of heme oxygenase suggests that it is a PEST protein, i.e., targeted for rapid turnover.
引用
收藏
页码:300 / 305
页数:6
相关论文
共 32 条
[1]   NEOPLASTIC TRANSFORMATION OF NEWBORN RAT ASTROCYTES IN CULTURE [J].
BRESSLER, JP ;
DEVELLIS, J .
BRAIN RESEARCH, 1985, 348 (01) :21-27
[2]  
CHIANG HL, 1988, J BIOL CHEM, V263, P6797
[3]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[4]  
CRUSE I, 1988, J BIOL CHEM, V263, P3348
[5]   REGULATION OF HEAT-SHOCK PROTEIN-SYNTHESIS IN RAT ASTROCYTES [J].
DWYER, BE ;
NISHIMURA, RN ;
DEVELLIS, J ;
CLEGG, KB .
JOURNAL OF NEUROSCIENCE RESEARCH, 1991, 28 (03) :352-358
[6]  
DWYER BE, 1990, AM SOC NEUR ABSTR, V20, P128
[7]  
FLIGIEL SEG, 1984, AM J PATHOL, V115, P418
[8]  
ISHIZAWA S, 1983, J BIOL CHEM, V258, P4220
[10]  
KEYSE SM, 1987, J BIOL CHEM, V262, P14821