Searching for depolarization-induced genes that modulate synaptic plasticity and neurotrophin-induced genes that mediate neuronal differentiation

被引:14
作者
Herschman, HR
Ferguson, GD
Feldman, JD
Farias-Eisner, R
Vician, L
机构
[1] Univ Calif Los Angeles, Inst Mol Biol, Dept Biol Chem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Pharmacol, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Pediat, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA
[5] Univ Calif Los Angeles, Inst Brain Res, Los Angeles, CA 90095 USA
关键词
depolarization; forskolin; nerve growth factor; synaptotagmin; UPAR; PC12; cells;
D O I
10.1023/A:1007546600535
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We identify and characterize two classes of immediate-early genes: (i) genes, induced by depolarization in neurons, that play a role in depolarization-induced neuronal plasticity and (ii) genes, induced in neuronal precursors by neurotrophins, that play a causal role in neurotrophin-directed neuronal differentiation. We use rat PC12 pheochromocytoma cells to identify (i) genes preferentially induced by [depolarization or forskolin] versus [Nerve Growth Factor (NGF) or Epidermal Growth Factor (EGF)] and (ii) genes preferentially induced by NGF versus EGF, We describe (i) a collection of genes preferentially induced by depolarization/forskolin in PC12 cells and by kainic acid in vivo, and (ii) a collection of genes preferentially induced by NGF. The synaptotagmin IV gene encodes a synaptic vesicle protein whose level is modulated by depolarization. NGF preferentially induces the urokinase-plasminogen activator receptor in PC12 cells. Antisense oligonucleotide and anti-UPAR antibody experiments demonstrate that NGF induced UPAR expression is required for NGF-driven PC12 cell differentiation.
引用
收藏
页码:591 / 602
页数:12
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