• Medientyp: E-Artikel
  • Titel: Molecular determinants of voltage-gated sodium channel regulation by the Nedd4/Nedd4-like proteins
  • Beteiligte: Rougier, Jean-Sébastien; van Bemmelen, Miguel X.; Bruce, M. Christine; Jespersen, Thomas; Gavillet, Bruno; Apothéloz, Florine; Cordonier, Sophie; Staub, Olivier; Rotin, Daniela; Abriel, Hugues
  • Erschienen: American Physiological Society, 2005
  • Erschienen in: American Journal of Physiology-Cell Physiology
  • Sprache: Englisch
  • DOI: 10.1152/ajpcell.00460.2004
  • ISSN: 0363-6143; 1522-1563
  • Schlagwörter: Cell Biology ; Physiology
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  • Beschreibung: <jats:p> The voltage-gated Na<jats:sup>+</jats:sup> channels (Na<jats:sub>v</jats:sub>) form a family composed of 10 genes. The COOH termini of Na<jats:sub>v</jats:sub> contain a cluster of amino acids that are nearly identical among 7 of the 10 members. This COOH-terminal sequence, PPSYDSV, is a PY motif known to bind to WW domains of E3 protein-ubiquitin ligases of the Nedd4 family. We recently reported that cardiac Na<jats:sub>v</jats:sub>1.5 is regulated by Nedd4-2. In this study, we further investigated the molecular determinants of regulation of Na<jats:sub>v</jats:sub> proteins. When expressed in HEK-293 cells and studied using whole cell voltage clamping, the neuronal Na<jats:sub>v</jats:sub>1.2 and Na<jats:sub>v</jats:sub>1.3 were also downregulated by Nedd4-2. Pull-down experiments using fusion proteins bearing the PY motif of Na<jats:sub>v</jats:sub>1.2, Na<jats:sub>v</jats:sub>1.3, and Na<jats:sub>v</jats:sub>1.5 indicated that mouse brain Nedd4-2 binds to the Na<jats:sub>v</jats:sub> PY motif. Using intrinsic tryptophan fluorescence imaging of WW domains, we found that Na<jats:sub>v</jats:sub>1.5 PY motif binds preferentially to the fourth WW domain of Nedd4-2 with a K<jats:sub>d</jats:sub> of ∼55 μM. We tested the binding properties and the ability to ubiquitinate and downregulate Na<jats:sub>v</jats:sub>1.5 of three Nedd4-like E3s: Nedd4-1, Nedd4-2, and WWP2. Despite the fact that along with Nedd4-2, Nedd4-1 and WWP2 bind to Na<jats:sub>v</jats:sub>1.5 PY motif, only Nedd4-2 robustly ubiquitinated and downregulated Na<jats:sub>v</jats:sub>1.5. Interestingly, coexpression of WWP2 competed with the effect of Nedd4-2. Finally, using brefeldin A, we found that Nedd4-2 accelerated internalization of Na<jats:sub>v</jats:sub>1.5 stably expressed in HEK-293 cells. This study shows that Nedd4-dependent ubiquitination of Na<jats:sub>v</jats:sub> channels may represent a general mechanism regulating the excitability of neurons and myocytes via modulation of channel density at the plasma membrane. </jats:p>
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