BACKGROUND AND PURPOSE: Calcium-activated chloride channels (CaCCs) are key depolarizing mechanisms that have an important role in vascular smooth muscle contraction. Here, we investigated whether these channels are regulated by phosphatidylinositol (4,5) bisphosphate [P(4,5)P2 ], a known regulator of various ion channels. EXPERIMENTAL APPROACH: Calcium-activated Cl(-) currents (IClCa ) were recorded by patch clamp electrophysiology of rat isolated pulmonary artery smooth muscle cells. TMEM16A protein-phosphoinositide interaction was studied by co-immunoprecipitation and phosphoinositide binding arrays on protein lysates from whole pulmonary arteries and HEK293 cells overexpressing TMEM16A, the molecular correlate. KEY RESULTS: PI(4,5)P2 and other phospholipids were shown to bind directly to TMEM16A isolated from whole pulmonary artery (PA) and TMEM16A-eGFP expressed in HEK293 cells. Agents that reduced PI(4,5)P2 levels through different routes [PLC activation, PI4K inhibition, PI(4,5)P2 scavenging and absorption] all increased IClCa evoked by solutions containing clamped-free [Ca(2+) ], whereas enrichment of activating solutions with PI(4,5)P2 inhibited IClca in PA smooth muscle cells with approximately 50% reduction at 1 μM. CONCLUSIONS AND IMPLICATIONS: These data are the first to show a negative regulation of TMEM16A-encoded CaCCs by PI(4,5)P2 and propose that control of PI(4,5)P2 levels is a key determinant of arterial physiology.
BACKGROUND AND PURPOSE: Calcium-activated chloride channels (CaCCs) are key depolarizing mechanisms that have an important role in vascular smooth muscle contraction. Here, we investigated whether these channels are regulated by phosphatidylinositol (4,5) bisphosphate [P(4,5)P2 ], a known regulator of various ion channels. EXPERIMENTAL APPROACH: Calcium-activated Cl(-) currents (IClCa ) were recorded by patch clamp electrophysiology of rat isolated pulmonary artery smooth muscle cells. TMEM16A protein-phosphoinositide interaction was studied by co-immunoprecipitation and phosphoinositide binding arrays on protein lysates from whole pulmonary arteries and HEK293 cells overexpressing TMEM16A, the molecular correlate. KEY RESULTS:PI(4,5)P2 and other phospholipids were shown to bind directly to TMEM16A isolated from whole pulmonary artery (PA) and TMEM16A-eGFP expressed in HEK293 cells. Agents that reduced PI(4,5)P2 levels through different routes [PLC activation, PI4K inhibition, PI(4,5)P2 scavenging and absorption] all increased IClCa evoked by solutions containing clamped-free [Ca(2+) ], whereas enrichment of activating solutions with PI(4,5)P2 inhibited IClca in PA smooth muscle cells with approximately 50% reduction at 1 μM. CONCLUSIONS AND IMPLICATIONS: These data are the first to show a negative regulation of TMEM16A-encoded CaCCs by PI(4,5)P2 and propose that control of PI(4,5)P2 levels is a key determinant of arterial physiology.
Authors: Alison J Davis; Abigail S Forrest; Thomas A Jepps; Maria L Valencik; Michael Wiwchar; Cherie A Singer; William R Sones; Iain A Greenwood; Normand Leblanc Journal: Am J Physiol Cell Physiol Date: 2010-08-04 Impact factor: 4.249
Authors: Ramon J Ayon; Matthew B Hawn; Joydeep Aoun; Michael Wiwchar; Abigail S Forrest; Fiona Cunningham; Cherie A Singer; Maria L Valencik; Iain A Greenwood; Normand Leblanc Journal: Am J Physiol Cell Physiol Date: 2019-08-28 Impact factor: 4.249
Authors: Henry R Askew Page; Thomas Dalsgaard; Samuel N Baldwin; Thomas A Jepps; Oleksandr Povstyan; Søren P Olesen; Iain A Greenwood Journal: Br J Pharmacol Date: 2019-04-11 Impact factor: 8.739
Authors: Peter R Strege; Simon J Gibbons; Amelia Mazzone; Cheryl E Bernard; Arthur Beyder; Gianrico Farrugia Journal: Am J Physiol Gastrointest Liver Physiol Date: 2017-03-23 Impact factor: 4.052