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Nedd4-2-dependent regulation of astrocytic Kir4.1 and Connexin43 controls neuronal network activity.
Altas, Bekir; Rhee, Hong-Jun; Ju, Anes; Solís, Hugo Cruces; Karaca, Samir; Winchenbach, Jan; Kaplan-Arabaci, Oykum; Schwark, Manuela; Ambrozkiewicz, Mateusz C; Lee, ChungKu; Spieth, Lena; Wieser, Georg L; Chaugule, Viduth K; Majoul, Irina; Hassan, Mohamed A; Goel, Rashi; Wojcik, Sonja M; Koganezawa, Noriko; Hanamura, Kenji; Rotin, Daniela; Pichler, Andrea; Mitkovski, Miso; de Hoz, Livia; Poulopoulos, Alexandros; Urlaub, Henning; Jahn, Olaf; Saher, Gesine; Brose, Nils; Rhee, JeongSeop; Kawabe, Hiroshi.
Afiliação
  • Altas B; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Rhee HJ; International Max Planck Research School and the Göttingen Graduate School for Neurosciences, Biophysics and Molecular Biosciences , Göttingen, Germany.
  • Ju A; The Göttingen Graduate School for Neurosciences, Biophysics, and Molecular Biosciences, PhD Program Systems Neuroscience, University of Göttingen , Göttingen, Germany.
  • Solís HC; Department of Pharmacology and Program in Neuroscience, University of Maryland School of Medicine, Baltimore, MD, USA.
  • Karaca S; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Winchenbach J; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Kaplan-Arabaci O; The Göttingen Graduate School for Neurosciences, Biophysics, and Molecular Biosciences, PhD Program Systems Neuroscience, University of Göttingen , Göttingen, Germany.
  • Schwark M; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Ambrozkiewicz MC; International Max Planck Research School and the Göttingen Graduate School for Neurosciences, Biophysics and Molecular Biosciences , Göttingen, Germany.
  • Lee C; Department of Neurogenetics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Spieth L; International Max Planck Research School and the Göttingen Graduate School for Neurosciences, Biophysics and Molecular Biosciences , Göttingen, Germany.
  • Wieser GL; Bioanalytical Mass Spectrometry Group, Max Planck Institute for Multidisciplinary Sciences , Göttingen, Germany.
  • Chaugule VK; The Göttingen Graduate School for Neurosciences, Biophysics, and Molecular Biosciences, PhD Program Systems Neuroscience, University of Göttingen , Göttingen, Germany.
  • Majoul I; Department of Neurogenetics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Hassan MA; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Goel R; The Göttingen Graduate School for Neurosciences, Biophysics, and Molecular Biosciences, PhD Program Molecular Physiology of the Brain, University of Göttingen , Göttingen, Germany.
  • Wojcik SM; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Koganezawa N; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Hanamura K; International Max Planck Research School and the Göttingen Graduate School for Neurosciences, Biophysics and Molecular Biosciences , Göttingen, Germany.
  • Rotin D; Institute of Cell Biology and Neurobiology, Charité-Universitätsmedizin Berlin , Corporate Member of Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Berlin, Germany.
  • Pichler A; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Mitkovski M; Department of Neurogenetics, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • de Hoz L; City Campus Light Microscopy Facility, Max Planck Institute for Multidisciplinary Sciences , Göttingen, Germany.
  • Poulopoulos A; Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics, Freiburg, Germany.
  • Urlaub H; Institute of Biology, Center for Structural and Cell Biology in Medicine, University of Lübeck, Lübeck, Germany.
  • Jahn O; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Saher G; Protein Research Department, Genetic Engineering and Biotechnology Research Institute (GEBRI), City of Scientific Research and Technological Applications (SRTA-City), New Borg El-Arab City, Egypt.
  • Brose N; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Rhee J; Department of Molecular Neurobiology, Max Planck Institute for Multidisciplinary Sciences, Göttingen, Germany.
  • Kawabe H; Department of Pharmacology, Gunma University Graduate School of Medicine, Maebashi, Japan.
J Cell Biol ; 223(1)2024 01 01.
Article em En | MEDLINE | ID: mdl-38032389
ABSTRACT
Nedd4-2 is an E3 ubiquitin ligase in which missense mutation is related to familial epilepsy, indicating its critical role in regulating neuronal network activity. However, Nedd4-2 substrates involved in neuronal network function have yet to be identified. Using mouse lines lacking Nedd4-1 and Nedd4-2, we identified astrocytic channel proteins inwardly rectifying K+ channel 4.1 (Kir4.1) and Connexin43 as Nedd4-2 substrates. We found that the expression of Kir4.1 and Connexin43 is increased upon conditional deletion of Nedd4-2 in astrocytes, leading to an elevation of astrocytic membrane ion permeability and gap junction activity, with a consequent reduction of γ-oscillatory neuronal network activity. Interestingly, our biochemical data demonstrate that missense mutations found in familial epileptic patients produce gain-of-function of the Nedd4-2 gene product. Our data reveal a process of coordinated astrocytic ion channel proteostasis that controls astrocyte function and astrocyte-dependent neuronal network activity and elucidate a potential mechanism by which aberrant Nedd4-2 function leads to epilepsy.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Permeabilidade da Membrana Celular / Astrócitos / Conexina 43 / Canais de Potássio Corretores do Fluxo de Internalização / Ubiquitina-Proteína Ligases Nedd4 Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Permeabilidade da Membrana Celular / Astrócitos / Conexina 43 / Canais de Potássio Corretores do Fluxo de Internalização / Ubiquitina-Proteína Ligases Nedd4 Limite: Animals / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article