Reinhold D S, Neet K E
Department of Biochemistry, Case Western Reserve University, Cleveland, Ohio 44106.
J Biol Chem. 1989 Feb 25;264(6):3538-44.
Nerve growth factor (NGF) causes pheochromocytoma cells (PC12) to undergo a number of physiological changes which mimic the differentiated neuronal cell, including neurite extension. We have examined protein kinase C (Ca2+/phospholipid-dependent enzyme) as a potential signaling mechanism in NGF-stimulated neurite outgrowth and induction of the enzyme ornithine decarboxylase. Phorbol 12-myristate 13-acetate (PMA) can activate protein kinase C and induce ornithine decarboxylase in PC12 cells with kinetics which are similar to those of NGF induction, but only to levels about 10-fold lower. The induction of ornithine decarboxylase by both NGF and PMA is inhibited by cycloheximide and actinomycin D suggesting that both agents increase enzyme activity by increasing gene transcription. The evidence presented here, however, shows that the induction produced by the two agents is through two different pathways. First, maximal induction by NGF is increased when PMA is included in the media showing that the two effects are synergistic. Second, NGF does not cause induction of ornithine decarboxylase in the mutant PC12nnr5 cell line (Green, S.H., Rydel, R.E., Connolly, J.L., and Greene, L.A. (1986) J. Cell Biol. 103, 1967-1978) while added PMA does produce an induction of the enzyme. Finally, when protein kinase C is down-regulated by incubating PC12 cells with PMA in serum-containing or serum-free medium for 24 h, the induction by PMA is completely inhibited, while the NGF induction is not affected. A recent study (Hall, F.L., Fernyhough, P., Ishii, D.N., and Vulliet, P.R. (1988) J. Biol. Chem. 263, 4460-4466) using sphingosine inhibition concluded that protein kinase C was required for NGF-stimulated neuritogenesis. In contrast, results presented here show that down-regulation of protein kinase C also has no effect on NGF-mediated neurite extension in PC12 cells grown in serum-free medium. Our data demonstrate that induction of ornithine decarboxylase and formation of neurites in PC12 cells by NGF does not require a protein kinase C-mediated pathway.
神经生长因子(NGF)可使嗜铬细胞瘤细胞(PC12)发生一些类似于分化神经元细胞的生理变化,包括神经突延伸。我们研究了蛋白激酶C(一种Ca2 + /磷脂依赖性酶)作为NGF刺激神经突生长及诱导鸟氨酸脱羧酶过程中的一种潜在信号传导机制。佛波酯12 - 肉豆蔻酸酯13 - 乙酸酯(PMA)可激活蛋白激酶C并诱导PC12细胞中的鸟氨酸脱羧酶,其动力学与NGF诱导相似,但诱导水平仅低约10倍。NGF和PMA对鸟氨酸脱羧酶的诱导均受到环己酰亚胺和放线菌素D的抑制,这表明两种试剂均通过增加基因转录来提高酶活性。然而,此处提供的证据表明,两种试剂产生的诱导作用是通过两条不同途径。首先,当培养基中加入PMA时,NGF的最大诱导作用增强,表明两种效应具有协同作用。其次,NGF不会在突变型PC12nnr5细胞系中诱导鸟氨酸脱羧酶(Green, S.H., Rydel, R.E., Connolly, J.L., and Greene, L.A. (1986) J. Cell Biol. 103, 1967 - 1978),而添加的PMA确实会诱导该酶的产生。最后,当通过在含血清或无血清培养基中用PMA孵育PC12细胞24小时来下调蛋白激酶C时,PMA的诱导作用被完全抑制,而NGF的诱导作用不受影响。最近一项使用鞘氨醇抑制作用的研究(Hall, F.L., Fernyhough, P., Ishii, D.N., and Vulliet, P.R. (1988) J. Biol. Chem. 263, 4460 - 4466)得出结论,蛋白激酶C是NGF刺激神经突生成所必需的。相反,此处给出的结果表明,下调蛋白激酶C对在无血清培养基中生长的PC12细胞中NGF介导的神经突延伸也没有影响。我们的数据表明,NGF诱导PC12细胞中的鸟氨酸脱羧酶及神经突形成并不需要蛋白激酶C介导的途径。