INSULIN-LIKE GROWTH-FACTOR-II PROMOTES IN-VITRO CHOLINERGIC DEVELOPMENT OF MOUSE SEPTAL NEURONS - COMPARISON WITH THE EFFECTS OF INSULIN-LIKE GROWTH-FACTOR-I

被引:47
作者
KONISHI, Y
TAKAHASHI, K
CHUI, DH
ROSENFELD, RG
HIMENO, M
TABIRA, T
机构
[1] NATL CTR NEUROL & PSYCHIAT,NATL INST NEUROSCI,DIV DEMYELINATING DIS & AGING,KODAIRA,TOKYO 187,JAPAN
[2] STANFORD UNIV,SCH MED,DEPT PEDIAT ENDOCRINOL,STANFORD,CA 94305
[3] KYUSHU UNIV,FAC PHARMACEUT SCI,DEPT BIOCHEM,FUKUOKA 812,JAPAN
基金
日本科学技术振兴机构;
关键词
INSULIN-LIKE GROWTH FACTOR; CHOLINERGIC NEURON; INSULIN-LIKE GROWTH FACTOR II RECEPTOR; CATION INDEPENDENT MANNOSE-6-PHOSPHATE RECEPTOR; NEUROTROPHIC FACTOR; CHOLINE ACETYLTRANSFERASE;
D O I
10.1016/0006-8993(94)91048-0
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We investigated the effect of insulin-like growth factors II and I (IGFII and IGFI) on septal primary cultures from mouse embryonic day 15 brains. The addition of IGFII to septal cultures enhanced total choline acetyltransferase (ChAT) activity in a dose-dependent manner. Maximal stimulation of ChAT activity was observed at 10 ng/ml IGFII. The effect of IGFII on ChAT activity was completely blocked by anti-IGFII/M-6-P receptor antibodies, whereas the antisera alone had no effect on the enzyme activity. Double-labeled immunohistochemical studies revealed that most ChAT-positive neurons expressed IGFII/M-6-P receptor immunoreactivity. These results indicate that the trophic effect of IGFII results from the direct action of this molecule through the IGFII/M-6-P receptor in septal cholinergic neurons. IGFI also stimulated ChAT activity, but with less potency than IGFII. Antibodies against the IGFII/M-6-P receptor inhibited approximately 50% of the IGFI response, suggesting that the effect of IGFI is mediated in part by the IGFII/M-6-P receptor. Thus, it appears that IGFII and IGFI are potent trophic factors for central cholinergic neurons and could potentially play a significant role in the differentiation, maintenance and regeneration of these neurons.
引用
收藏
页码:53 / 61
页数:9
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