Chemin Jean, Mezghrani Alexandre, Bidaud Isabelle, Dupasquier Sebastien, Marger Fabrice, Barrère Christian, Nargeot Joël, Lory Philippe
Département de Physiologie, Institut de Génomique Fonctionnelle, CNRS UMR 5203, INSERM U661, Universités de Montpellier 1 et 2, Institut Fédératif de Recherche 3, 141 Rue de la Cardonille, Montpellier, France.
J Biol Chem. 2007 Nov 9;282(45):32710-8. doi: 10.1074/jbc.M702746200. Epub 2007 Sep 12.
Modulation of low voltage-activated Ca(V)3 T-type calcium channels remains poorly characterized compared with high voltage-activated Ca(V)1 and Ca(V)2 calcium channels. Notably, it is yet unresolved whether Ca(V)3 channels are modulated by protein kinases in mammalian cells. In this study, we demonstrate that protein kinase A (PKA) and PKC (but not PKG) activation induces a potent increase in Ca(V)3.1, Ca(V)3.2, and Ca(V)3.3 currents in various mammalian cell lines. Notably, we show that protein kinase effects occur at physiological temperature ( approximately 30-37 degrees C) but not at room temperature ( approximately 22-27 degrees C). This temperature dependence could involve kinase translocation, which is impaired at room temperature. A similar temperature dependence was observed for PKC-mediated increase in high voltage-activated Ca(V)2.3 currents. We also report that neither Ca(V)3 surface expression nor T-current macroscopic properties are modified upon kinase activation. In addition, we provide evidence for the direct phosphorylation of Ca(V)3.2 channels by PKA in in vitro assays. Overall, our results clearly establish the role of PKA and PKC in the modulation of Ca(V)3 T-channels and further highlight the key role of the physiological temperature in the effects described.
与高电压激活的Ca(V)1和Ca(V)2钙通道相比,低电压激活的Ca(V)3 T型钙通道的调节机制仍未得到充分表征。值得注意的是,Ca(V)3通道是否在哺乳动物细胞中受蛋白激酶调节仍未明确。在本研究中,我们证明蛋白激酶A(PKA)和蛋白激酶C(PKC,而非蛋白激酶G)的激活会导致多种哺乳动物细胞系中Ca(V)3.1、Ca(V)3.2和Ca(V)3.3电流显著增加。值得注意的是,我们发现蛋白激酶的作用发生在生理温度(约30 - 37摄氏度)下,而在室温(约22 - 27摄氏度)下则不会发生。这种温度依赖性可能涉及激酶转位,而在室温下激酶转位会受损。在PKC介导的高电压激活的Ca(V)2.3电流增加中也观察到了类似的温度依赖性。我们还报告称,激酶激活后,Ca(V)3的表面表达和T电流宏观特性均未改变。此外,我们在体外实验中提供了PKA直接磷酸化Ca(V)3.2通道的证据。总体而言,我们的结果明确了PKA和PKC在Ca(V)3 T通道调节中的作用,并进一步强调了生理温度在所描述效应中的关键作用。