Charpentier G, Fournier F, Behue N, Marlot D, Brule G
Laboratoire de Neurobiologie Cellulaire, Uniersité de Picardie Jules Verne, Faculté des Sciences, Amiens, France.
Proc Biol Sci. 1993 Oct 22;254(1339):15-20. doi: 10.1098/rspb.1993.0120.
The slow inward Na current observed during sustained depolarization of the Xenopus oocyte membrane is due to a complex mechanism described as the induction of the channels. The present work investigates the role of protein phosphorylation in Na channel function. Injection of alkaline phosphatase in the oocytes decreased inward current. Therefore, the possible involvement of protein kinase in Na channel induction was explored. Treatment of oocytes with two activators of protein kinase C (PKC) resulted in enhanced Na current amplitude, whereas the treatment of oocytes with two potent PKC inhibitors decreased the inward current. These results imply that PKC phosphorylation is a fundamental step of Na channel induction. The possibility that the depolarization of the oocyte membrane may be the factor involved in PKC activation is discussed.
在非洲爪蟾卵母细胞膜持续去极化过程中观察到的缓慢内向钠电流,是由一种被描述为通道诱导的复杂机制引起的。目前的研究工作探讨了蛋白质磷酸化在钠通道功能中的作用。向卵母细胞中注射碱性磷酸酶会使内向电流降低。因此,研究人员探究了蛋白激酶在钠通道诱导过程中可能发挥的作用。用两种蛋白激酶C(PKC)激活剂处理卵母细胞,会使钠电流幅度增强,而用两种强效PKC抑制剂处理卵母细胞,则会使内向电流降低。这些结果表明,PKC磷酸化是钠通道诱导的一个基本步骤。本文还讨论了卵母细胞膜去极化可能是参与PKC激活的因素这一可能性。