Presynaptic and Ca2+-independent PKC subspecies modulates NMDAR1 current

被引:11
作者
Koga, T
Sakai, N
Tanaka, C
Saito, N
机构
[1] KOBE UNIV,BIOSIGNAL RES CTR,MOLEC PHARMACOL LAB,NADA KU,KOBE 657,JAPAN
[2] KOBE UNIV,SCH MED,DEPT PHARMACOL,KOBE 650,JAPAN
关键词
NMDA receptor; protein kinase C; subspecies; calcium; metabotropic glutamate receptor; Xenopus oocyte;
D O I
10.1097/00001756-199601310-00024
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
WE have studied the properties of the protein kinase C (PKC) subspecies that modulates the NMDA receptor (NMDAR1). The current through homomeric NMDAR1 expressed in Xenopus oocytes was increased by 200-500% by phorbol ester and also by activation of a metabotropic glutamate receptor (mGluR1) expressed in the same oocytes. This potentiation of the NMDAR1 current was not inhibited by the intracellular injection of EGTA. Intracellular injection of epsilon-PKC, a presynaptic PKC subspecies, potentiated the NMDAR1 current more efficiently than did the Ca2+-dependent gamma-PKC, a postsynaptic subspecies of the enzyme. Our findings suggested that the presynaptic NMDA receptor could be potentiated in a Ca2+-independent manner by the activation of presynaptic PKC subspecies.
引用
收藏
页码:477 / 480
页数:4
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