The novel compound TDN-345 induces synthesis/secretion of nerve growth factor in C6-10A glioma cells

被引:5
作者
Fukumoto, H [1 ]
Kakihana, M [1 ]
Kaisho, Y [1 ]
Suno, M [1 ]
机构
[1] TAKEDA CHEM IND LTD,PHARMACEUT DISCOVERY RES DIV,RES MANAGEMENT DEPT,TSUKUBA,IBARAKI 30042,JAPAN
关键词
TDN-345; C6-10A; astrocytoma; nerve growth factor; neurotrophic factor; induction;
D O I
10.1016/S0006-8993(97)81691-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
A novel compound, TDN-345, not bearing catechol moiety, induced NGF synthesis/secretion in C6-10A glioma cells. Both intracellular and extracellular nerve growth factor (NGF) protein levels increased within 3 h and reached a maximum around 12 h after the addition of TDN-345. The induction of NGF synthesis/secretion by TDN-345 occurred in a concentration-dependent manner, beginning with about 0.1 mu M and reaching a maximum at 10 mu M. The ED50 was 0.88 mu M. The induction was accompanied by an increase in NGF mRNA but not beta-actin mRNA. In a time-course study, the NGF mRNA level was found to reach a maximum 2-3 h after the addition of TDN-345 and then to return to control levels. The induction occurred dose-dependently. The catecholaminergic compound epinephrine, which induces NGF synthesis/secretion, increased the intracellular cyclic AMP content by more than 1000-times at 10 mu M. In contrast, TDN-345 did not cause such a prominent increase in cAMP even at 100 mu M. These results indicate that TDN-345 induces NGF synthesis/secretion by increasing NGF mRNA expression, and the action of TDN-345 clearly differs from that of epinephrine, as it does not seem to involve cAMP as a second messenger. The results of the present study suggest the existence of a signal transduction pathway for NGF synthesis/secretion which is not mediated by cAMP. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:87 / 93
页数:7
相关论文
共 43 条
[2]   EXPRESSION OF THE BETA-NERVE GROWTH-FACTOR GENE IN HIPPOCAMPAL-NEURONS [J].
AYERLELIEVRE, C ;
OLSON, L ;
EBENDAL, T ;
SEIGER, A ;
PERSSON, H .
SCIENCE, 1988, 240 (4857) :1339-1341
[3]   DIFFERENTIATED RAT GLIAL CELL STRAIN IN TISSUE CULTURE [J].
BENDA, P ;
LIGHTBODY, J ;
SATO, G ;
LEVINE, L ;
SWEET, W .
SCIENCE, 1968, 161 (3839) :370-+
[4]   THE POTENTIAL FOR TREATING NEURODEGENERATIVE DISORDERS WITH NGF-INDUCING COMPOUNDS [J].
CARSWELL, S .
EXPERIMENTAL NEUROLOGY, 1993, 124 (01) :36-42
[5]   ISOLATION OF BIOLOGICALLY-ACTIVE RIBONUCLEIC-ACID FROM SOURCES ENRICHED IN RIBONUCLEASE [J].
CHIRGWIN, JM ;
PRZYBYLA, AE ;
MACDONALD, RJ ;
RUTTER, WJ .
BIOCHEMISTRY, 1979, 18 (24) :5294-5299
[6]   Transmitter timecourse in the synaptic cleft: Its role in central synaptic function [J].
Clements, JD .
TRENDS IN NEUROSCIENCES, 1996, 19 (05) :163-171
[7]   ALZHEIMERS-DISEASE - A DISORDER OF CORTICAL CHOLINERGIC INNERVATION [J].
COYLE, JT ;
PRICE, DL ;
DELONG, MR .
SCIENCE, 1983, 219 (4589) :1184-1190
[8]   NEUROTRANSMITTER-RELATED ENZYMES IN SENILE DEMENTIA OF THE ALZHEIMER TYPE [J].
DAVIES, P .
BRAIN RESEARCH, 1979, 171 (02) :319-327
[9]  
DAVIES P, 1976, LANCET, V2, P1403
[10]   AMELIORATION OF CHOLINERGIC NEURON ATROPHY AND SPATIAL MEMORY IMPAIRMENT IN AGED RATS BY NERVE GROWTH-FACTOR [J].
FISCHER, W ;
WICTORIN, K ;
BJORKLUND, A ;
WILLIAMS, LR ;
VARON, S ;
GAGE, FH .
NATURE, 1987, 329 (6134) :65-68