Lory P, Nargeot J
Centre de Recherche de Biochimie Macromoleculaire, UPR 8402 CNRS, U 249 INSERM, Montpellier, France.
Biochem Biophys Res Commun. 1992 Feb 14;182(3):1059-65. doi: 10.1016/0006-291x(92)91839-i.
Cyclic AMP-dependent modulation of cardiac L-type voltage-dependent Ca channel (VDCC) has been probed in Xenopus laevis oocytes injected with poly(A+) RNA from rat heart. A 2 to 3 fold increase of the Ba current amplitude was routinely obtained upon microinjection of cAMP (50-500 microM). Inhibition of protein kinase A (PKA) dramatically reduced the Ba current amplitude, indicating that cAMP-dependent modulation plays an important role in maintaining the basal activity of expressed Ca channels. Moreover, the effects of the DHP agonist Bay K 8644 on kinetic properties of expressed Ba current (IBa,C) were dependent on PKA activation. The results suggest that most expressed cardiac L-type VDCCs are phosphorylated and demonstrate that reconstitution in Xenopus oocytes is a suitable approach to address how phosphorylation regulates VDCC activity.
利用从大鼠心脏提取的聚腺苷酸(poly(A+))RNA注射到非洲爪蟾卵母细胞中,对环磷酸腺苷(cAMP)依赖性调节心脏L型电压依赖性钙通道(VDCC)进行了研究。显微注射cAMP(50 - 500微摩尔)后,钡电流幅度通常会增加2至3倍。蛋白激酶A(PKA)的抑制显著降低了钡电流幅度,表明cAMP依赖性调节在维持所表达钙通道的基础活性中起重要作用。此外,二氢吡啶(DHP)激动剂Bay K 8644对所表达钡电流(IBa,C)动力学特性的影响取决于PKA的激活。结果表明,大多数所表达的心脏L型VDCCs被磷酸化,并且证明在非洲爪蟾卵母细胞中的重组是研究磷酸化如何调节VDCC活性的合适方法。