<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Laedermann CJ</dc:creator>
  <dc:creator>Decosterd I</dc:creator>
  <dc:creator>Abriel H</dc:creator>
  <dc:date>2014</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Ion channel proteins are regulated by different types of posttranslational modifications. The focus of this review is the regulation of voltage-gated sodium channels (Navs) upon their ubiquitylation. The amiloride-sensitive epithelial sodium channel (ENaC) was the first ion channel shown to be regulated upon ubiquitylation. This modification results from the binding of ubiquitin ligase from the Nedd4 family to a protein-protein interaction domain, known as the PY motif, in the ENaC subunits. Many of the Navs have similar PY motifs, which have been demonstrated to be targets of Nedd4-dependent ubiquitylation, tagging them for internalization from the cell surface. The role of Nedd4-dependent regulation of the Nav membrane density in physiology and disease remains poorly understood. Two recent studies have provided evidence that Nedd4-2 is downregulated in dorsal root ganglion (DRG) neurons in both rat and mouse models of nerve injury-induced neuropathic pain. Using two different mouse models, one with a specific knockout of Nedd4-2 in sensory neurons and another where Nedd4-2 was overexpressed with the use of viral vectors, it was demonstrated that the neuropathy-linked neuronal hyperexcitability was the result of Nav1.7 and Nav1.8 overexpression due to Nedd4-2 downregulation. These studies provided the first in vivo evidence of the role of Nedd4-2-dependent regulation of Nav channels in a disease state. This ubiquitylation pathway may be involved in the development of symptoms and diseases linked to Nav-dependent hyperexcitability, such as pain, cardiac arrhythmias, epilepsy, migraine, and myotonias.</dc:description>
  <dc:identifier>https://sonar.ch/global/documents/183268</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.1007/978-3-642-41588-3_11</dc:relation>
  <dc:relation>info:eu-repo/semantics/altIdentifier/pmid/24737239</dc:relation>
  <dc:source>Handbook of experimental pharmacology. - 2014</dc:source>
  <dc:subject xmlns:ns1="xml" ns1:lang="en">Action Potentials</dc:subject>
  <dc:subject xmlns:ns2="xml" ns2:lang="en">Animals</dc:subject>
  <dc:subject xmlns:ns3="xml" ns3:lang="en">Endosomal Sorting Complexes Required for Transport</dc:subject>
  <dc:subject xmlns:ns4="xml" ns4:lang="en">Epithelial Sodium Channels</dc:subject>
  <dc:subject xmlns:ns5="xml" ns5:lang="en">Humans</dc:subject>
  <dc:subject xmlns:ns6="xml" ns6:lang="en">Ion Channel Gating</dc:subject>
  <dc:subject xmlns:ns7="xml" ns7:lang="en">Nedd4 Ubiquitin Protein Ligases</dc:subject>
  <dc:subject xmlns:ns8="xml" ns8:lang="en">Protein Binding</dc:subject>
  <dc:subject xmlns:ns9="xml" ns9:lang="en">Protein Interaction Domains and Motifs</dc:subject>
  <dc:subject xmlns:ns10="xml" ns10:lang="en">Protein Isoforms</dc:subject>
  <dc:subject xmlns:ns11="xml" ns11:lang="en">Signal Transduction</dc:subject>
  <dc:subject xmlns:ns12="xml" ns12:lang="en">Sodium</dc:subject>
  <dc:subject xmlns:ns13="xml" ns13:lang="en">Ubiquitin-Protein Ligases</dc:subject>
  <dc:subject xmlns:ns14="xml" ns14:lang="en">Ubiquitination</dc:subject>
  <dc:subject xmlns:ns15="xml" ns15:lang="en">Voltage-Gated Sodium Channels</dc:subject>
  <dc:title xmlns:ns16="xml" ns16:lang="en">Ubiquitylation of voltage-gated sodium channels.</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
