Studies of the effect of ionomycin on the KCNQ4 channel expressed in Xenopus oocytes

• Published in: Biochemical and biophysical research communications Vol. 348; no. 1; pp. 295 - 300
• Main Authors: Su, Ching-Chyuan, Li, Shuan-Yow, Yang, Jiann-Jou, Su, Mao-Chang, Lin, Min-Jon
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.09.2006
• Subjects: Animals; BAPTA-AM; Bepridil - pharmacology; Calcium; Calcium - metabolism; Channel; Electrophysiology; Indoles - pharmacology; Ion Channel Gating - drug effects; Ionomycin; Ionomycin - pharmacology; Ionophores - pharmacology; KCNQ Potassium Channels - drug effects; KCNQ Potassium Channels - physiology; KCNQ4; Oocytes - metabolism; Pyridines - pharmacology; Xenopus laevis; KCNQ4; Ionomycin; Calcium; Channel; BAPTA-AM
• ISSN: 0006-291X; 1090-2104
• DOI: 10.1016/j.bbrc.2006.07.053

The effect of ionomycin on the human KCNQ4 channels expressed in Xenopus leavis oocytes was investigated. KCNQ4 channels expressed in Xenopus oocytes were measured using two-electrode voltage clamp. The activation of KCNQ4 current had slow activation kinetics and low threshold (∼−50 mV). The expressed current of KCNQ4 showed the half-maximal activation ( V 1/2) was −17.8 mV and blocked almost completely by KCNQ4 channel blockers, linopirdine (300 μM) or bepridil (200 μM). The significant increase of KCNQ4 outward current induced by ionomycin (calcium salt) is about 1.7-fold of control current amplitude at +60 mV and shifted V 1/2 by approximately −8 mV (from −17.8 to −26.0 mV). This effect of ionomycin could be reversed by the further addition of BAPTA-AM (0.3 mM), a membrane–permeable calcium chelator. Furthermore, the increased effect of ionomycin on KCNQ4 current is abolished by pretreatment of linopirdine or bepridil. In contrast, direct cytoplasmic injection of calcium medium (up to 1 mM calcium, 50 nl) did not mimic the effect of ionomycin. In conclusion, the effect of ionomycin on enhancement of KCNQ4 current is independent of intracellular calcium mobilization and possibly acts on intramembrane hydrophobic site of KCNQ4 protein expressed in Xenopus oocytes.