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| Hauptseite > Publikationsdatenbank > Endosomal 2Cl-/H+ exchangersregulate neuronal excitability Bytuning Kv7/KCNQ channel density > print |
| Hauptseite > Publikationsdatenbank > Endosomal 2Cl-/H+ exchangersregulate neuronal excitability Bytuning Kv7/KCNQ channel density > print |
| 001 | 1043576 | ||
| 005 | 20260123203311.0 | ||
| 024 | 7 | _ | |a 10.1093/brain/awaf243 |2 doi |
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| 100 | 1 | _ | |a Guzman, Raul |0 P:(DE-Juel1)156375 |b 0 |
| 245 | _ | _ | |a Endosomal 2Cl-/H+ exchangersregulate neuronal excitability Bytuning Kv7/KCNQ channel density |
| 260 | _ | _ | |a Oxford |c 2025 |b Oxford Univ. Press |
| 336 | 7 | _ | |a article |2 DRIVER |
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| 500 | _ | _ | |a This work was funded by the German Research Foundation (DFG) (GU 2042/2-1 to R.E.G.) and the European Union’s Horizon 2020 Framework Programme for Research and Innovation under the Human Brain Project Framework Partnership Agreement (HBP FPA) (No. 650003 to D.F.). |
| 520 | _ | _ | |a CLCN3 and CLCN4 encode the endosomal 2Cl−/H+ exchangers ClC-3 and ClC-4, which are highly expressed within the CNS, including the hippocampal formation. Pathogenic variants recently found in these genes have given rise to the rare CLCN3- and CLCN4-related neurodevelopmental conditions, characterized by a range of neurological and neuropsychiatric complications, such as global developmental delay, intellectual disability as a core feature, seizures, behavioural issues and brain abnormalities. The mechanisms by which ClC-3 and ClC-4 regulate neuronal function and viability, in addition to the molecular pathways affected in CLCN3- and CLCN4-related neurodevelopmental conditions, remain unknown. In neurodegenerative diseases, neuronal dendrites undergo pathological changes often associated with aberrant electrical activity.To investigate how ClC-3 or ClC-4 deficit alters neuronal excitability and morphology, we combined patch-clamp recordings in acute hippocampal slice preparations with simultaneous intracellular biocytin filling. We analysed the functional and structural properties of Clcn3−/− and Clcn4−/− neurons. Two firing patterns are found in the cornu ammonis 2 (CA2) region of the hippocampus: regular and burst firing. At postnatal Day 13, 62% of the assessed CA2 wild-type neurons showed a rhythmic bursting behaviour; this was reduced to 19% in Clcn4−/− and completely absent in the Clcn3−/− condition. Changes in the firing patterns were accompanied by a depolarizing shift in the action potential threshold and an increase in the after-hyperpolarizing phase of the action potentials. Blockade of Kv7/KCNQ and, to a lesser extent, Kv1, but not BK, SK or Kv2 channels, recapitulates the wild-type firing pattern phenotype in the Clcn3−/− condition. Moreover, we detected abnormalities in the complexity of the dendritic arborization. Branching and lengths of apical and basal domains were significantly reduced in the Clcn3−/− neurons and moderately altered in the Clcn4−/− neurons. At postnatal Day 3, we found 25% of bursting neurons in Clcn3−/− with no significant morphological abnormalities in the dendritic arborization in comparison to the wild-type, suggesting that functional defects precede structural changes in Cl−/H+ exchanger-deficient neurons. Likewise, dentate granule cells exhibited defective action potential properties and reduced burst-firing activity, which was substantially but not fully rescued by Kv7/KCNQ blockage.We conclude that Cl−/H+ exchangers regulate the electrical excitability and firing patterns of neurons primarily by fine- tuning Kv7/KCNQ channel density, and that functional defects might contribute to alterations in dendritic morphology. Our findings provide new insights into the underlying molecular mechanisms of Cl−/H+ exchangers in neurons and pave the way for potential therapeutic interventions for CLCN3- and CLCN4-related patients associated with disruption of Cl−/H+ exchange function. |
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| 536 | _ | _ | |a DFG project G:(GEPRIS)430631456 - Funktionelle Rolle der intrazellulären Chlorid/Proton Austauscher ClC-3, ClC-4 und ClC-5 in der Neurosekretion (430631456) |0 G:(GEPRIS)430631456 |c 430631456 |x 2 |
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| 773 | _ | _ | |a 10.1093/brain/awaf243 |0 PERI:(DE-600)1474117-9 |p 4299–4314 |t Brain |v 148 |y 2025 |x 0006-8950 |
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