TY - JOUR T1 - Amyloid Precursor Protein (APP) Controls the Expression of the Transcriptional Activator Neuronal PAS Domain Protein 4 (NPAS4) and Synaptic GABA Release JF - eneuro JO - eNeuro DO - 10.1523/ENEURO.0322-19.2020 VL - 7 IS - 3 SP - ENEURO.0322-19.2020 AU - Rémi Opsomer AU - Sabrina Contino AU - Florian Perrin AU - Roberta Gualdani AU - Bernadette Tasiaux AU - Pierre Doyen AU - Maxime Vergouts AU - Céline Vrancx AU - Anna Doshina AU - Nathalie Pierrot AU - Jean-Noël Octave AU - Philippe Gailly AU - Serena Stanga AU - Pascal Kienlen-Campard Y1 - 2020/05/01 UR - http://www.eneuro.org/content/7/3/ENEURO.0322-19.2020.abstract N2 - The amyloid precursor protein (APP) has been extensively studied as the precursor of the β-amyloid (Aβ) peptide, the major component of the senile plaques found in the brain of Alzheimer’s disease (AD) patients. However, the function of APP per se in neuronal physiology remains to be fully elucidated. APP is expressed at high levels in the brain. It resembles a cell adhesion molecule or a membrane receptor, suggesting that its function relies on cell-cell interaction and/or activation of intracellular signaling pathways. In this respect, the APP intracellular domain (AICD) was reported to act as a transcriptional regulator. Here, we used a transcriptome-based approach to identify the genes transcriptionally regulated by APP in the rodent embryonic cortex and on maturation of primary cortical neurons. Surprisingly, the overall transcriptional changes were subtle, but a more detailed analysis pointed to genes clustered in neuronal-activity dependent pathways. In particular, we observed a decreased transcription of neuronal PAS domain protein 4 (NPAS4) in APP−/− neurons. NPAS4 is an inducible transcription factor (ITF) regulated by neuronal depolarization. The downregulation of NPAS4 co-occurs with an increased production of the inhibitory neurotransmitter GABA and a reduced expression of the GABAA receptors α1. CRISPR-Cas-mediated silencing of NPAS4 in neurons led to similar observations. Patch-clamp investigation did not reveal any functional decrease of GABAA receptors activity, but long-term potentiation (LTP) measurement supported an increased GABA component in synaptic transmission of APP−/− mice. Together, NPAS4 appears to be a downstream target involved in APP-dependent regulation of inhibitory synaptic transmission. ER -