{ "labelLang" : "hun", "responseDate" : "2024-03-28 17:25", "content" : { "otype" : "JournalArticle", "mtid" : 31953914, "status" : "VALIDATED", "published" : true, "comment" : "AstraZeneca-Tufts Laboratory of Basic and Translational Neuroscience, United States \n Department of Neuroscience, Tufts University School of Medicine, Boston, MA, United States \n Department of Neuroscience, Physiology, and Pharmacology, University College London, London, United Kingdom \n Neuroscience, IMED Biotech Unit, AstraZeneca, Boston, MA, United States \n Export Date: 7 April 2021 \n CODEN: JBCHA \n Correspondence Address: Moss, S.J.; AstraZeneca-Tufts Laboratory of Basic and Translational NeuroscienceUnited States; email: Stephen.Moss@Tufts.edu\nFunding Agency and Grant Number: National Institutes of Health (NIH); National Institute of Neurological Disorders and StrokeUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Neurological Disorders & Stroke (NINDS) [NS051195, NS056359, NS081735, NS087662, NS108378, R21NS080064, R21NS111338, R21NS111064]; NIH, United Sates; National Institute of Mental HealthUnited States Department of Health & Human ServicesNational Institutes of Health (NIH) - USANIH National Institute of Mental Health (NIMH) [MH097446]; AstraZeneca Postdoctoral Program, United StatesAstraZeneca\n Funding text: This work is supported by National Institutes of Health (NIH); National Institute of Neurological Disorders and Stroke Grants NS051195 (S. J. M.), NS056359 (S. J. M.), NS081735 (S. J. M.), NS087662 (S. J. M.), NS108378 (S. J. M. and P. A. D.), R21NS080064 (S. J. M.), R21NS111338 (P. A. D.), R21NS111064 (P. A. D.); NIH, United Sates; National Institute of Mental Health Grant MH097446 (S. J. M. and P. A. D.). G. K. was a fellow of and funded by the AstraZeneca Postdoctoral Program, United States. 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2295, "snippet" : true }, "volume" : "296", "internalId" : "100364", "firstPageOrInternalIdForSort" : "100364", "publishedYear" : 2021, "abstractText" : "The K+/Cl− cotransporter KCC2 (SLC12A5) allows mature neurons in the CNS to maintain low intracellular Cl− levels that are critical in mediating fast hyperpolarizing synaptic inhibition via type A γ-aminobutyric acid receptors (GABAARs). In accordance with this, compromised KCC2 activity results in seizures, but whether such deficits directly contribute to the subsequent changes in neuronal structure and viability that lead to epileptogenesis remains to be assessed. Canonical hyperpolarizing GABAAR currents develop postnatally, which reflect a progressive increase in KCC2 expression levels and activity. To investigate the role that KCC2 plays in regulating neuronal viability and architecture, we have conditionally ablated KCC2 expression in developing and mature neurons. Decreasing KCC2 expression in mature neurons resulted in the rapid activation of the extrinsic apoptotic pathway. Intriguingly, direct pharmacological inhibition of KCC2 in mature neurons was sufficient to rapidly induce apoptosis, an effect that was not abrogated via blockade of neuronal depolarization using tetrodotoxin (TTX). In contrast, ablating KCC2 expression in immature neurons had no discernable effects on their subsequent development, arborization, or dendritic structure. However, removing KCC2 in immature neurons was sufficient to ablate the subsequent postnatal development of hyperpolarizing GABAAR currents. Collectively, our results demonstrate that KCC2 plays a critical role in neuronal survival by limiting apoptosis, and mature neurons are highly sensitive to the loss of KCC2 function. 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