LONG-TERM EXPRESSION OF THE C-FOS PROTEIN DURING THE INVITRO DIFFERENTIATION OF CEREBELLAR GRANULE CELLS INDUCED BY POTASSIUM OR NMDA

被引:36
作者
DIDIER, M
ROUX, P
PIECHACZYK, M
MANGEAT, P
DEVILLIERS, G
BOCKAERT, J
PIN, JP
机构
[1] SANOFI RECH,LIGNE NEUROPSYCHIAT,MONTPELLIER,FRANCE
[2] UNIV MONTPELLIER 2,BIOL MOLEC LAB,F-34060 MONTPELLIER,FRANCE
[3] CNRS,CTR PHARMACOL ENDOCRINOL,INSERM,F-34033 MONTPELLIER,FRANCE
来源
MOLECULAR BRAIN RESEARCH | 1992年 / 12卷 / 1-3期
关键词
N-METHYL-D-ASPARTATE; NEUROTROPHIC FACTOR; CEREBELLAR GRANULE CELL; C-FOS PROTEIN; DEVELOPMENT;
D O I
10.1016/0169-328X(92)90091-O
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Levels of the c-fos protein were assayed in mouse cerebellar granule cells during their in vitro development under different culture conditions. When grown in media favoring both their survival and differentiation, i.e. in the presence of 30 mM K+ or 12.5 mM K+ plus 100-mu-M N-methyl-D-aspartate (NMDA), the c-fos protein becomes detectable in the nucleus of granule cells on and after 6 days and persists to high levels until the culture begins to decline. The protein c-fos appears therefore after the critical period described for the survival effect of K+ depolarization or NMDA receptor stimulation which corresponds to days 2-5 after plating. The c-fos protein remains however scarcely detectable or undetectable throughout the life-span of cells cultured under conditions providing poor survival and differentiation, i.e. in the presence of low K+ (5 or 12.5 mM) alone or when the effect of NMDA is blocked by the NMDA receptor antagonist MK-801. Interestingly, in cortical and striatal neurons, the survival and differentiation of which being not affected by depolarizing media, no c-fos protein is detected whatever the culture conditions tested at least during the first 18 days in vitro. This suggests that long-term expression of the c-fos gene might be related to some aspect of the late in vitro differentiation process of cerebellar granule cells.
引用
收藏
页码:249 / 258
页数:10
相关论文
共 59 条
[41]   DIFFERENTIATION OF F9 TERATOCARCINOMA STEM-CELLS AFTER TRANSFER OF C-FOS PROTO-ONCOGENES [J].
MULLER, R ;
WAGNER, EF .
NATURE, 1984, 311 (5985) :438-442
[42]   ANTISENSE RNA OF PROTOONCOGENE C-FOS BLOCKS RENEWED GROWTH OF QUIESCENT 3T3 CELLS [J].
NISHIKURA, K ;
MURRAY, JM .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (02) :639-649
[43]  
Palay S. L., 1974, CEREBELLAR CORTEX
[44]   GLUTAMATE ACTING ON NMDA RECEPTORS STIMULATES NEURITE OUTGROWTH FROM CEREBELLAR GRANULE CELLS [J].
PEARCE, IA ;
CAMBRAYDEAKIN, MA ;
BURGOYNE, RD .
FEBS LETTERS, 1987, 223 (01) :143-147
[45]   DEREGULATED C-FOS EXPRESSION INTERFERES WITH NORMAL BONE-DEVELOPMENT IN TRANSGENIC MICE [J].
RUTHER, U ;
GARBER, C ;
KOMITOWSKI, D ;
MULLER, R ;
WAGNER, EF .
NATURE, 1987, 325 (6103) :412-416
[46]   CONVULSANT-INDUCED INCREASE IN TRANSCRIPTION FACTOR MESSENGER-RNAS IN RAT-BRAIN [J].
SAFFEN, DW ;
COLE, AJ ;
WORLEY, PF ;
CHRISTY, BA ;
RYDER, K ;
BARABAN, JM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (20) :7795-7799
[47]   EXPRESSION OF C-FOS PROTEIN IN BRAIN - METABOLIC MAPPING AT THE CELLULAR-LEVEL [J].
SAGAR, SM ;
SHARP, FR ;
CURRAN, T .
SCIENCE, 1988, 240 (4857) :1328-1331
[48]   MEMBRANE DEPOLARIZATION AND CALCIUM INDUCE C-FOS TRANSCRIPTION VIA PHOSPHORYLATION OF TRANSCRIPTION FACTOR CREB [J].
SHENG, M ;
MCFADDEN, G ;
GREENBERG, ME .
NEURON, 1990, 4 (04) :571-582
[49]   THE REGULATION AND FUNCTION OF C-FOS AND OTHER IMMEDIATE EARLY GENES IN THE NERVOUS-SYSTEM [J].
SHENG, M ;
GREENBERG, ME .
NEURON, 1990, 4 (04) :477-485
[50]   GLUTAMATE RECEPTOR AGONISTS INCREASE THE EXPRESSION OF FOS, FRA, AND AP-1 DNA-BINDING ACTIVITY IN THE MAMMALIAN BRAIN [J].
SONNENBERG, JL ;
MITCHELMORE, C ;
MACGREGORLEON, PF ;
HEMPSTEAD, J ;
MORGAN, JI ;
CURRAN, T .
JOURNAL OF NEUROSCIENCE RESEARCH, 1989, 24 (01) :72-80