| Literature DB >> 33373327 |
Lara Pizzamiglio1, Elisa Focchi1, Clara Cambria1, Luisa Ponzoni2, Silvia Ferrara1, Francesco Bifari1, Genni Desiato3, Nicoletta Landsberger1, Luca Murru2, Maria Passafaro2, Mariaelvina Sala2, Michela Matteoli2,3, Elisabetta Menna2,3, Flavia Antonucci1.
Abstract
Impairment of the GABAergic system has been reported in epilepsy, autism, attention deficit hyperactivity disorder, and schizophrenia. We recently demonstrated that ataxia telangiectasia mutated (ATM) directly shapes the development of the GABAergic system. Here, we show for the first time to our knowledge how the abnormal expression of ATM affects the pathological condition of autism. We exploited 2 different animal models of autism, the methyl CpG binding protein 2-null (Mecp2y/-) mouse model of Rett syndrome and mice prenatally exposed to valproic acid, and found increased ATM levels. Accordingly, treatment with the specific ATM kinase inhibitor KU55933 (KU) normalized molecular, functional, and behavioral defects in these mouse models, such as (a) delayed GABAergic development, (b) hippocampal hyperexcitability, (c) low cognitive performances, and (d) social impairments. Mechanistically, we demonstrate that KU administration to WT hippocampal neurons leads to (a) higher early growth response 4 activity on Kcc2b promoter, (b) increased expression of Mecp2, and (c) potentiated GABA transmission. These results provide evidence and molecular substrates for the pharmacological development of ATM inhibition in autism spectrum disorders.Entities:
Keywords: Development; Molecular pathology; Mouse models; Neurological disorders; Neuroscience
Year: 2021 PMID: 33373327 PMCID: PMC7934840 DOI: 10.1172/jci.insight.133654
Source DB: PubMed Journal: JCI Insight ISSN: 2379-3708