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Na+ Channel ß Subunits: Overachievers of the Ion Channel Family

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JournalFrontiers in Pharmacology
DatePublished - 28 Sep 2011
Volume2
Number of pages11
Original languageEnglish

Abstract

Voltage-gated Na(+) channels (VGSCs) in mammals contain a pore-forming a subunit and one or more ß subunits. There are five mammalian ß subunits in total: ß1, ß1B, ß2, ß3, and ß4, encoded by four genes: SCN1B-SCN4B. With the exception of the SCN1B splice variant, ß1B, the ß subunits are type I topology transmembrane proteins. In contrast, ß1B lacks a transmembrane domain and is a secreted protein. A growing body of work shows that VGSC ß subunits are multifunctional. While they do not form the ion channel pore, ß subunits alter gating, voltage-dependence, and kinetics of VGSCa subunits and thus regulate cellular excitability in vivo. In addition to their roles in channel modulation, ß subunits are members of the immunoglobulin superfamily of cell adhesion molecules and regulate cell adhesion and migration. ß subunits are also substrates for sequential proteolytic cleavage by secretases. An example of the multifunctional nature of ß subunits is ß1, encoded by SCN1B, that plays a critical role in neuronal migration and pathfinding during brain development, and whose function is dependent on Na(+) current and ¿-secretase activity. Functional deletion of SCN1B results in Dravet Syndrome, a severe and intractable pediatric epileptic encephalopathy. ß subunits are emerging as key players in a wide variety of physiopathologies, including epilepsy, cardiac arrhythmia, multiple sclerosis, Huntington's disease, neuropsychiatric disorders, neuropathic and inflammatory pain, and cancer. ß subunits mediate multiple signaling pathways on different timescales, regulating electrical excitability, adhesion, migration, pathfinding, and transcription. Importantly, some ß subunit functions may operate independently of a subunits. Thus, ß subunits perform critical roles during development and disease. As such, they may prove useful in disease diagnosis and therapy.

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Copyright: © 2011 Brackenbury and Isom. This is an open-access article subject to a non-exclusive license between the authors and Frontiers Media SA, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and other Frontiers conditions are complied with.

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