1. Functional specialization of different PI3K isoforms for the control of neuronal architecture, synaptic plasticity, and cognition
- Author
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Carla Sánchez-Castillo, María I. Cuartero, Alba Fernández-Rodrigo, Víctor Briz, Sergio López-García, Raquel Jiménez-Sánchez, Juan A. López, Mariona Graupera, José A. Esteban, Universidad de Alicante. Departamento de Fisiología, Genética y Microbiología, Neurobiología del Sistema Visual y Terapia de Enfermedades Neurodegenerativas (NEUROVIS), Ministerio de Ciencia e Innovación (España), Instituto de Salud Carlos III, Ministerio de Economía (España), Marie Curie, Intertalentum Postdoctoral Program, Fundación ProCNIC, Ministerio de Ciencia e Innovación. Centro de Excelencia Severo Ochoa (España), Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF), and Agencia Estatal de Investigación (España)
- Subjects
Multidisciplinary ,Functional specialization ,Neuronal architecture ,Cognitive performance ,PI3K isoforms ,Synaptic plasticity - Abstract
Neuronal connectivity and activity-dependent synaptic plasticity are fundamental properties that support brain function and cognitive performance. Phosphatidylinositol 3-kinase (PI3K) intracellular signaling controls multiple mechanisms mediating neuronal growth, synaptic structure, and plasticity. However, it is still unclear how these pleiotropic functions are integrated at molecular and cellular levels. To address this issue, we used neuron-specific virally delivered Cre expression to delete either p110α or p110β (the two major catalytic isoforms of type I PI3K) from the hippocampus of adult mice. We found that dendritic and postsynaptic structures are almost exclusively supported by p110α activity, whereas p110β controls neurotransmitter release and metabotropic glutamate receptor-dependent long-term depression at the presynaptic terminal. In addition to these separate functions, p110α and p110β jointly contribute to N-methyl-d-aspartate receptor-dependent postsynaptic long-term potentiation. This molecular and functional specialization is reflected in different proteomes controlled by each isoform and in distinct behavioral alterations for learning/memory and sociability in mice lacking p110α or p110β. This work was supported by the Spanish Ministry of Science and Innovation grants SAF2017-86983-R and PID2020-117651RB (to J.A.E.), Spanish Ministry of Science and Innovation grants SAF2017-89116R-P (FEDER/EU) and PID2020-116184RB (to M.G.), Carlos III Institute of Health-Fondo de Investigación Sanitaria grant PRB3 (IPT17/0019–ISCIII-SGEFI/ERDF, ProteoRed) and CIBERCV (to J.A.L.), Spanish Ministry of Economy postdoctoral contract IJCI-2015-25507 (to M.I.C.), Marie Curie cofund UAM-UE (EU project 713366) Intertalentum Postdoctoral Program (to V.B.), and Spanish Ministry of Science and Innovation predoctoral contracts (to C.S.-C., A.F.-R., and S.L.-G.). The CNIC is supported by the Instituto de Salud Carlos III (ISCIII), the Ministerio de Ciencia e Innovación (MCIN), and the Pro CNIC Foundation, and is a Severo Ochoa Center of Excellence (grant CEX2020-001041-S funded by MICIN/AEI/10.13039/501100011033). Sí
- Published
- 2022