Kyushu University Academic Staff Educational and Research Activities Database
List of Presentations
Yasunari Sakai Last modified dateļ¼š2023.11.22

Associate Professor / Department of Clinical Medicine / Faculty of Medical Sciences


Presentations
1. Yasunari Sakai, HYPERACTIVE MTOR SIGNALS IN THE PROOPIOMELANOCORTIN-EXPRESSING HIPPOCAMPAL NEURONS CAUSE AGE-DEPENDENT EPILEPSY AND PREMATURE DEATH IN MICE, American Epilepsy Society Annual Meeting, 2016.12, RATIONALE:
Epilepsy is a frequent comorbidity in patients with focal cortical dysplasia (FCD). Recent studies utilizing massive sequencing data identified subsets of genes that are associated with epilepsy and FCD. AKT and mTOR-related signals have been recently implicated in the pathogenic processes of epilepsy and FCD.
METHODS:
To clarify the functional roles of the AKT-mTOR pathway in the hippocampal neurons, we generated conditional knockout mice harboring the deletion of Pten (Pten-cKO) in Proopiomelanocortin-expressing neurons.
RESULTS:
The Pten-cKO mice developed normally until 8 weeks of age, then presented generalized seizures at 8-10 weeks of age. Video-monitored electroencephalograms detected paroxysmal discharges emerging from the cerebral cortex and hippocampus. These mice showed progressive hypertrophy of the dentate gyrus (DG) with increased expressions of excitatory synaptic markers (Psd95, Shank3 and Homer). In contrast, the expression of inhibitory neurons (Gad67) was decreased at 6-8 weeks of age. Immunofluorescence studies revealed the abnormal sprouting of mossy fibers in the DG of the Pten-cKO mice prior to the onset of seizures. The treatment of these mice with an mTOR inhibitor rapamycin successfully prevented the development of seizures and reversed these molecular phenotypes.
CONCLUSIONS:
The present study indicate that the mTOR pathway regulates hippocampal excitability in the postnatal brain.
FUNDING:
JSPS KAKEN No. 15K09624, Japan Life Science Foundation, Takeda Science Foundation, The Mother and Child Health Foundation, and the Japan Epilepsy Research Foundation.
2. Searching for the molecular pathways underlying pathogenesis of autism.