Ramakers G M, De Graan P N, Urban I J, Kraay D, Tang T, Pasinelli P, Oestreicher A B, Gispen W H
Department of Medical Pharmacology, Rudolf Magnus Institute for Neurosciences, University of Utrecht, The Netherlands.
J Biol Chem. 1995 Jun 9;270(23):13892-8. doi: 10.1074/jbc.270.23.13892.
The phosphorylation state of two identified neuralspecific protein kinase C substrates (the presynaptic protein B-50 and the postsynaptic protein neurogranin) was monitored after the induction of long term potentiation in the CA1 field of rat hippocampus slices by quantitative immunoprecipitation following 32Pi labeling in the recording chamber. B-50 phosphorylation was increased from 10 to 60 min, but no longer at 90 min after long term potentiation had been induced, neurogranin phosphorylation only at 60 min. Increased phosphorylation was not found when long term potentiation was blocked with the N-methyl-D-aspartate receptor antagonist D-2-amino-5-phosphonovalerate, when only low frequency stimulation was applied or tetanic stimulation failed to induce long term-potentiation. Our data show that both B-50 and neurogranin phosphorylation are increased following the induction of long term potentiation, thus providing strong evidence for pre- and postsynaptic protein kinase C activation during narrow, partially overlapping, time windows after the induction of long term potentiation.
在记录室用³²P标记后,通过定量免疫沉淀法监测大鼠海马切片CA1区诱导长时程增强(LTP)后,两种已确定的神经特异性蛋白激酶C底物(突触前蛋白B - 50和突触后蛋白神经颗粒素)的磷酸化状态。长时程增强诱导后,B - 50磷酸化在10至60分钟增加,但在90分钟时不再增加,神经颗粒素磷酸化仅在60分钟时增加。当用N - 甲基 - D - 天冬氨酸受体拮抗剂D - 2 - 氨基 - 5 - 磷酸戊酸阻断长时程增强时,当仅施加低频刺激或强直刺激未能诱导长时程增强时,未发现磷酸化增加。我们的数据表明,长时程增强诱导后,B - 50和神经颗粒素的磷酸化均增加,从而为长时程增强诱导后狭窄、部分重叠的时间窗口内突触前和突触后蛋白激酶C的激活提供了有力证据。