bioRxivNeurosciencePreprint
GIRK Channel Loss of Function Increases Dendritic Excitability in a Mouse Model of GNB1 Encephalopathy
Samuel GritziD, Anshul Voleti, Matthew S. ScarnatiiD, Alessandro R. GalloniiD, Aaron D. MilsteiniD
Abstract
GNB1 encephalopathy (GNB1-E) is a rare neurodevelopmental disorder associated with motor dysfunction, epilepsy and learning disability caused by mutations in the gene encoding the G protein subunit G{beta}1. Previous work has shown that altered G{beta}1 can disrupt activation of G-protein-coupled inwardly rectifying potassium (GIRK) channels, dysregulate neuronal excitability and cause seizures. However, the relevant upstream regulators of G{beta}1 and the consequences of GIRK dysfunction for neuronal synaptic, cellular and circuit function have not been characterized. Here we report that mice of both sexes carrying the deleterious p.I80T mutation in Gnb1 present features consistent with GNB1-E, including developmental delay, decreased locomotion and increased anxiety. Using histology, whole-cell patch-clamp electrophysiology and pharmacology in ex vivo brain slices, we find that hippocampal neurons in heterozygous Gnb1I80T/+ mice exhibit simplified dendritic morphologies, decreased synaptic inhibition mediated by metabotropic GABAB receptors and increased dendritic excitability. These phenotypes result in longer duration dendritic calcium spikes in response to synaptic afferent stimulation, an effect that is reversed by a specific activator of GIRK channels, ML297. Given the known roles of dendritic calcium spikes in driving burst firing and inducing synaptic plasticity, these findings suggest that targeting dendritic excitability has therapeutic potential to address both the seizure susceptibility and learning deficits associated with GNB1-E. Significance StatementGNB1 encephalopathy (GNB1-E) is a rare neurodevelopmental disorder associated with motor dysfunction, epilepsy and learning disability for which there are currently no mechanism-based treatments. Here we show that a pathogenic variant of the G protein subunit G{beta}1 impairs activation of neuronal G-protein-coupled inwardly rectifying potassium (GIRK) channels by inhibitory synaptic GABAB receptors. This leads to increased dendritic excitability and longer duration dendritic calcium spikes in mouse hippocampal neurons in response to stimulation of synaptic inputs. We find that this phenotype is reversed by a drug that activates GIRK channels, opening pathways to develop therapies for GNB1-E that specifically target dendritic excitability.
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- G protein-coupled potassium channels implicated in mouse and cellular models of GNB1 Encephalopathy
Sophie Colombo, Sabrina Petri, … David B. Goldstein·bioRxiv·Jul 9, 2019
- Cross-species analysis of GNB1 I80T encephalopathy: conserved developmental, epileptic and neuronal transcriptome signatures
Haritha P. Reddy, Vigneshwar Ranjan, … Nathan Dascal·bioRxiv·Aug 7, 2026
- Complex synaptic and intrinsic interactions disrupt input/output functions in the hippocampus of Scn1b knockout mice
Jessica Hotard Chancey, Alisha A. Ahmed, … MacKenzie Allen Howard·Journal of NeurosciencePeer-reviewed·Oct 16, 2023
- Epilepsy and neurobehavioral abnormalities in mice with a KCNB1 pathogenic variant that alters conducting and non-conducting functions of KV2.1
Nicole A. Hawkins, Sunita N. Misra, … Jennifer A. Kearney·Neurobiology of DiseasePeer-reviewed·Oct 23, 2020
- A pathogenic missense mutation in kainate receptors elevates dendritic excitability and synaptic integration through dysregulation of SK channels
Toshihiro Nomura, Sakiko Taniguchi, … Anis Contractor·Journal of NeurosciencePeer-reviewed·Oct 6, 2023
- Preferential vulnerability of cortical GABAergic interneurons to Nalcn deficiency
Candela Barettino, Álvaro Ballesteros-Gonzalez, … Isabel del Pino·bioRxiv·Jan 21, 2026