Georg L. Wieser
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Georg L. Wieser has a total of 29 co-authors. Here are the top co-authors by number of shared publications:
- Alexandros Poulopoulos
Department of Pharmacology and Physiology, University of Maryland School of Medicine, Baltimore, Maryland
1 shared publication - Andrea Pichler
Department of Epigenetics, Max Planck Institute of Immunobiology and Epigenetics
1 shared publication - Anes Ju
Max Planck Institute for Multidisciplinary Sciences 1 Department of Molecular Neurobiology Göttingen, Germany
1 shared publication - Bekir Altas
Marquette University
1 shared publication - Choong-Ku Lee
Laboratory of Molecular Neurophysiology, Department of Physiology, Yonsei University Wonju College of Medicine, Wonju 26426, Republic of Korea
1 shared publication - Daniela Rotin
Cell & Systems Biology Program, The Hospital for Sick Children, Toronto, Canada
1 shared publication
Latest Publications
- Open Access
- 30 November 2023
- Published by Rockefeller University Press in Journal of Cell Biology
- Vol. 223 (1)
Nedd4-2-dependent regulation of astrocytic Kir4.1 and Connexin43 controls neuronal network activity
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.
- 30 November 2023
- Published by Rockefeller University Press in Journal of Cell Biology
- Vol. 223 (1)
Open AccessNedd4-2-dependent regulation of astrocytic Kir4.1 and Connexin43 controls neuronal network activity
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.