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Lidocaine promotes the trafficking and functional expression of Na(v)1.8 sodium channels in mammalian cells.

Publication Type:

Journal Article

Source:

J Neurophysiol, Volume 98, Issue 1, p.467-77 (2007)

Keywords:

Anesthetics, Local, Animals, Animals, Newborn, Calnexin, Cells, Cultured, Dose-Response Relationship, Radiation, Electric Stimulation, Endoplasmic Reticulum, Ganglia, Spinal, Gene Expression Regulation, Humans, Immunohistochemistry, Lidocaine, Microscopy, Confocal, NAV1.8 Voltage-Gated Sodium Channel, Neurons, Protein Transport, Rats, Sodium Channels, Tetrodotoxin, Transfection

Abstract:

<p>Nociceptive neurons of the dorsal root ganglion (DRG) express a combination of rapidly gating TTX-sensitive and slowly gating TTX-resistant Na currents, and the channels that produce these currents have been cloned. The Na(v)1.7 and Na(v)1.8 channels encode for the rapidly inactivating TTX-sensitive and slowly inactivating TTX-resistant Na currents, respectively. Although the Na(v)1.7 channel expresses well in cultured mammalian cell lines, attempts to express the Na(v)1.8 channel using similar approaches has been met with limited success. The inability to heterologously express Na(v)1.8 has hampered detailed characterization of the biophysical properties and pharmacology of these channels. In this study, we investigated the determinants of Na(v)1.8 expression in tsA201 cells, a transformed variant of HEK293 cells, using a combination of biochemistry, immunochemistry, and electrophysiology. Our data indicate that the unusually low expression levels of Na(v)1.8 in tsA201 cells results from a trafficking defect that traps the channel protein in the endoplasmic reticulum. Incubating the cultured cells with the local anesthetic lidocaine dramatically enhanced the cell surface expression of functional Na(v)1.8 channels. The biophysical properties of the heterologously expressed Na(v)1.8 channel are similar but not identical to those of the TTX-resistant Na current of native DRG neurons, recorded under similar conditions. Our data indicate that the lidocaine acts as a molecular chaperone that promotes efficient trafficking and increased cell surface expression of Na(v)1.8 channels.</p>

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