Journal
JOURNAL OF NEUROSCIENCE
Volume 29, Issue 17, Pages 5654-5665Publisher
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.5978-08.2009
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Funding
- American Heart Association (AHA) Scientist Development [0635125N]
- National Institutes of Health (NIH) [DC01919, GM067154-01A1, GM067154, U24NS05060]
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Potassium channels activated by intracellular Na+ ions (K-Na) play several distinct roles in regulating the firing patterns of neurons, and, at the single channel level, their properties are quite diverse. Two known genes, Slick and Slack, encode K-Na channels. We have now found that Slick and Slack subunits coassemble to form heteromeric channels that differ from the homomers in their unitary conductance, kinetic behavior, subcellular localization, and response to activation of protein kinase C. Heteromer formation requires the N-terminal domain of Slack-B, one of the alternative splice variants of the Slack channel. This cytoplasmic N-terminal domain of Slack-B also facilitates the localization of heteromeric K-Na channels to the plasma membrane. Immunocytochemical studies indicate that Slick and Slack-B subunits are coexpressed in many central neurons. Our findings provide a molecular explanation for some of the diversity in reported properties of neuronal K-Na channels.
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