van Tol-Steye H, Lodder J C, Mansvelder H D, Planta R J, van Heerikhuizen H, Kits K S
Department of Neurophysiology, Research Institute Neurosciences, Faculty of Chemistry, Vrije Universiteit, 1081 HV Amsterdam, The Netherlands.
J Neurosci. 1999 May 15;19(10):3739-51. doi: 10.1523/JNEUROSCI.19-10-03739.1999.
Dopamine and the neuropeptides Ala-Pro-Gly-Trp-NH2 (APGWamide or APGWa) and Phe-Met-Arg-Phe-NH2 (FMRFamide or FMRFa) all activate an S-like potassium channel in the light green cells of the mollusc Lymnaea stagnalis, neuroendocrine cells that release insulin-related peptides. We studied the signaling pathways underlying the responses, the role of the G-protein betagamma subunit, and the interference by phosphorylation pathways. All responses are blocked by an inhibitor of arachidonic acid (AA) release, 4-bromophenacylbromide, and by inhibitors of lipoxygenases (nordihydroguaiaretic acid and AA-861) but not by indomethacin, a cyclooxygenase inhibitor. AA and phospholipase A2 (PLA2) induced currents with similar I-V characteristics and potassium selectivity as dopamine, APGWa, and FMRFa. PLA2 occluded the response to FMRFa. We conclude that convergence of the actions of dopamine, APGWa, and FMRFa onto the S-like channel occurs at or upstream of the level of AA and that formation of lipoxygenase metabolites of AA is necessary to activate the channel. Injection of a synthetic peptide, which interferes with G-protein betagamma subunits, inhibited the agonist-induced potassium current. This suggests that betagamma subunits mediate the response, possibly by directly coupling to a phospholipase. Finally, the responses to dopamine, APGWa, and FMRFa were inhibited by activation of PKA and PKC, suggesting that the responses are counteracted by PKA- and PKC-dependent phosphorylation. The PLA2-activated potassium current was inhibited by 8-chlorophenylthio-cAMP but not by 12-O-tetradecanoylphorbol 13-acetate (TPA). However, TPA did inhibit the potassium current induced by irreversible activation of the G-protein using GTP-gamma-S. Thus, it appears that PKA targets a site downstream of AA formation, e.g., the potassium channel, whereas PKC acts at the active G-protein or the phospholipase.
多巴胺以及神经肽丙氨酸 - 脯氨酸 - 甘氨酸 - 色氨酸 - 酰胺(APGWamide或APGWa)和苯丙氨酸 - 甲硫氨酸 - 精氨酸 - 苯丙氨酸 - 酰胺(FMRFamide或FMRFa)均可激活椎实螺(Lymnaea stagnalis)浅绿细胞中的一种S型钾通道,这些浅绿细胞是释放胰岛素相关肽的神经内分泌细胞。我们研究了这些反应背后的信号通路、G蛋白βγ亚基的作用以及磷酸化通路的干扰情况。所有反应均被花生四烯酸(AA)释放抑制剂4 - 溴苯甲酰溴以及脂氧合酶抑制剂(去甲二氢愈创木酸和AA - 861)阻断,但未被环氧化酶抑制剂吲哚美辛阻断。AA和磷脂酶A2(PLA2)诱导的电流具有与多巴胺、APGWa和FMRFa相似的电流 - 电压特性和钾选择性。PLA2可阻断对FMRFa的反应。我们得出结论,多巴胺、APGWa和FMRFa对S型通道的作用汇聚发生在AA水平或其上游,并且AA的脂氧合酶代谢产物的形成是激活该通道所必需的。注射一种干扰G蛋白βγ亚基的合成肽可抑制激动剂诱导的钾电流。这表明βγ亚基介导了该反应,可能是通过直接与磷脂酶偶联。最后,对多巴胺、APGWa和FMRFa的反应被蛋白激酶A(PKA)和蛋白激酶C(PKC)的激活所抑制,这表明这些反应被PKA和PKC依赖性磷酸化所抵消。PLA2激活的钾电流被8 - 氯苯硫基 - cAMP抑制,但未被12 - O - 十四酰佛波醇13 - 乙酸酯(TPA)抑制。然而,TPA确实抑制了使用GTP - γ - S对G蛋白进行不可逆激活所诱导的钾电流。因此,似乎PKA作用于AA形成下游的位点,例如钾通道,而PKC作用于活性G蛋白或磷脂酶。