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Acta Pharmacol Sin ; 37(1): 98-104, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26657057

ABSTRACT

AIM: Pirt is a two-transmembrane domain protein that regulates the function of a variety of ion channels. Our previous study indicated that Pirt acts as a positive endogenous regulator of the TRPM8 channel. The aim of this study was to investigate the mechanism underlying the regulation of TRPM8 channel by Pirt. METHODS: HEK293 cells were transfected with TRPM8+Pirt or TRPM8 alone. Menthol (1 mmol/L) was applied through perfusion to induce TRPM8-mediated voltage-dependent currents, which were recorded using a whole-cell recording technique. PIP2 (10 µmol/L) was added into the electrode pipettes (PI was taken as a control). Additionally, cell-attached single-channel recordings were conducted in CHO cells transfected with TRPM8+Pirt or TRPM8 alone, and menthol (1 mmol/L) was added into the pipette solution. RESULTS: Either co-transfection with Pirt or intracellular application of PIP2 (but not PI) significantly enhanced menthol-induced TRPM8 currents. Furthermore, Pirt and PIP2 synergistically modulated menthol-induced TRPM8 currents. Single-channel recordings revealed that co-transfection with Pirt significantly increased the single channel conductance. CONCLUSION: Pirt and PIP2 synergistically enhance TRPM8 channel activity, and Pirt regulates TRPM8 channel activity by increasing the single channel conductance.


Subject(s)
Carrier Proteins/metabolism , Membrane Proteins/metabolism , TRPM Cation Channels/metabolism , Carrier Proteins/genetics , HEK293 Cells , Humans , Ion Channel Gating , Membrane Proteins/genetics , Menthol/pharmacology , Phosphatidylinositol 4,5-Diphosphate/pharmacology , TRPM Cation Channels/genetics
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