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Contrasting effects of phosphatidylinositol 4,5‐bisphosphate on cloned TMEM16A and TMEM16B channels
Author(s) -
Ta Chau M,
Acheson Kathryn E,
Rorsman Nils J G,
Jongkind Remco C,
Tammaro Paolo
Publication year - 2017
Publication title -
british journal of pharmacology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.432
H-Index - 211
eISSN - 1476-5381
pISSN - 0007-1188
DOI - 10.1111/bph.13913
Subject(s) - phosphatidylinositol , chemistry , biophysics , patch clamp , phosphatase , gating , ion channel , microbiology and biotechnology , biochemistry , kinase , biology , phosphorylation , receptor
Background and Purpose Ca 2+ ‐activated Cl − channels (CaCCs) are gated open by a rise in intracellular Ca 2+ concentration ([Ca 2+ ] i ), typically provoked by activation of G q ‐protein coupled receptors (G q PCR). G q PCR activation initiates depletion of plasmalemmal phosphatidylinositol 4,5‐bisphosphate (PIP 2 ). Here, we determined whether PIP 2 acts as a signalling lipid for CaCCs coded by the TMEM16A and TMEM16B genes. Experimental Approach Patch‐clamp electrophysiology, in conjunction with genetically encoded systems to control cellular PIP 2 content, was used to define the mechanism of action of PIP 2 on TMEM16A and TMEM16B channels. Key Results A water‐soluble PIP 2 analogue (diC8‐PIP 2 ) activated TMEM16A channels by up to fivefold and inhibited TMEM16B by ~0.2‐fold. The effects of diC8‐PIP 2 on TMEM16A currents were especially pronounced at low [Ca 2+ ] i . In contrast, diC8‐PIP 2 modulation of TMEM16B channels did not vary over a broad [Ca 2+ ] i range but was only detectable at highly depolarized membrane potentials. Modulation of TMEM16A and TMEM16B currents was due to changes in channel gating, while single channel conductance was unaltered. Co‐expression of TMEM16A or TMEM16B with a Danio rerio voltage‐sensitive phosphatase (DrVSP), which degrades PIP 2 , led to reduction and enhancement of TMEM16A and TMEM16B currents respectively. These effects were abolished by an inactivating mutation in DrVSP and antagonized by simultaneous co‐expression of a phosphatidylinositol‐4‐phosphate 5‐kinase that catalyses PIP 2 formation. Conclusions and Implications PIP 2 acts as a modifier of TMEM16A and TMEM16B channel gating. Drugs interacting with PIP 2 signalling may affect TMEM16A and TMEM16B channel gating and have potential uses in basic science and implications for therapy.