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DOI: 10.1073/pnas.032678399
¤ OpenAccess: Green
This work has “Green” OA status. This means it may cost money to access on the publisher landing page, but there is a free copy in an OA repository.

Heteromultimers of DEG/ENaC subunits form H <sup>+</sup> -gated channels in mouse sensory neurons

Christopher J. Benson,Jinling Xie,John A. Wemmie,Margaret P. Price,Jillian Henss,Michael J. Welsh,Peter M. Snyder

Epithelial sodium channel
Dorsal root ganglion
Acid-sensing ion channel
2002
Acidic extracellular solution activates transient H(+)-gated currents in dorsal root ganglion (DRG) neurons. The biophysical properties of three degenerin/epithelial sodium (DEG/ENaC) channel subunits (BNC1, ASIC, and DRASIC), and their expression in DRG, suggest that they might underlie these H(+)-gated currents and function as sensory transducers. However, it is uncertain which of these DEG/ENaC subunits generate the currents, and whether they function as homomultimers or heteromultimers. We found that the biophysical properties of transient H(+)-gated currents from medium to large mouse DRG neurons differed from BNC1, ASIC, or DRASIC expressed individually, but were reproduced by coexpression of the subunits together. To test the contribution of each subunit, we studied DRG from three strains of mice, each bearing a targeted disruption of BNC1, ASIC, or DRASIC. Deletion of any one subunit did not abolish H(+)-gated currents, but altered currents in a manner consistent with heteromultimerization of the two remaining subunits. These data indicate that combinations of two or more DEG/ENaC subunits coassemble as heteromultimers to generate transient H(+)-gated currents in mouse DRG neurons.
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    Heteromultimers of DEG/ENaC subunits form H <sup>+</sup> -gated channels in mouse sensory neurons” is a paper by Christopher J. Benson Jinling Xie John A. Wemmie Margaret P. Price Jillian Henss Michael J. Welsh Peter M. Snyder published in 2002. It has an Open Access status of “green”. You can read and download a PDF Full Text of this paper here.