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Acid-sensing ion channels (ASICs) are a new and expanding family of proton-gated cation (Na+/Ca2+) channels that are widely expressed in sensory neurons and the central nervous system. Their distribution suggests that they may play a critical role in the sensation of the pain that accompanies tissue acidosis and may also be important in detecting the subtle pH variations that occur during neuronal signalling. Here, using whole-cell patch-clamp electrophysiology and reverse transcriptase-polymerase chain reaction (RT-PCR), we show that HEK293 cells, a commonly used cell line for the expression and characterisation of many ion channels, functionally express an endogenous proton-gated conductance attributable to the activity of human ASIC1a. These data therefore represent the first functional characterisation of hASIC1 and have many important implications for the use of HEK293 cells as a host cell system for the study of ASICs, vanilloid receptor-1 and any other proton-gated channel. With this latter point in mind we have devised a simple desensitisation strategy to selectively remove the contribution of hASIC1a from proton-gated currents recorded from HEK293 cells expressing vanilloid receptor-1.

Original publication

DOI

10.1007/s004240100584

Type

Journal article

Journal

Pflugers Arch

Publication Date

08/2001

Volume

442

Pages

668 - 674

Keywords

Acid Sensing Ion Channels, Amiloride, Cell Line, Diuretics, Humans, Hydrogen-Ion Concentration, Ion Channel Gating, Membrane Proteins, Nerve Tissue Proteins, Nociceptors, Patch-Clamp Techniques, Protons, Receptors, Drug, Reverse Transcriptase Polymerase Chain Reaction, Sodium Channels, TRPV Cation Channels