A Novel Tetrodotoxin-sensitive, Voltage-gated Sodium Channel Expressed in Rat and Human Dorsal Root Ganglia

• DOI: 10.1074/jbc.272.23.14805
• Publication Date: 2002-07-26T14:49:13Z
• Authors: Lakshmi Sangamesw...; Linda M. Fish; Bruce D. Koch; Douglas K. Rabert; Stephen G. Delgado; Mariola Ilnicka; Lyn B. Jakeman; Sanja Novakovic; Kimberley Wong; Ping Sze; Elda Tzoumaka; Gregory R. Stewart; Ronald C. Herman; Hardy Chan; Richard M. Eglen; John C. Hunter
• Keywords: Neurons; 0303 health sciences; DNA, Complementary; Transcription, Genetic; Macromolecular Substances; Molecular Sequence Data; NAV1.7 Voltage-Gated Sodium Channel; Neuropeptides; Tetrodotoxin; Polymerase Chain Reaction; Sodium Channels; Membrane Potentials; Rats; 3. Good health; 03 medical and health sciences; Organ Specificity; Ganglia, Spinal; Oocytes; Animals; Humans; Amino Acid Sequence; RNA, Messenger; Cloning, Molecular

Dorsal root ganglion neurons express a wide repertoire of sodium channels with different properties. Here, we report the cloning from rat, dorsal root ganglia (DRG), cellular expression, and functional analysis of a novel tetrodotoxin-sensitive peripheral sodium channel (PN), PN1. PN1 mRNA is expressed in many different tissues. Within the rat DRG, both the mRNA and PN1-like immunoreactivity are present in small and large neurons. The abundance of sodium channel mRNAs in rat DRG is rBI > PN1 >/= PN3 >>> rBIII by quantitative reverse transcription-polymerase chain reaction analysis. Data from reverse transcription-polymerase chain reaction and sequence analyses of human DRG and other human tissues suggest that rat PN1 is an ortholog of the human neuroendocrine channel. In Xenopus oocytes, PN1 exhibits kinetics that are similar to rBIIa sodium currents and is inhibited by tetrodotoxin with an IC50 of 4.3 +/- 0.92 nM. Unlike rBIIa, the inactivation kinetics of PN1 are not accelerated by the coexpression of the beta-subunits.