Consejo Superior de Investigaciones Científicas, Instituto Cajal, Madrid, Spain
Ricardo Gómez
Consejo Superior de Investigaciones Científicas, Instituto Cajal, Madrid, Spain; Cellular and Systems Neurobiology, Systems Biology Program, Centre for Genomic Regulation, The Barcelona Institute of Science and Technology, Barcelona, Spain
Sara Mederos
Consejo Superior de Investigaciones Científicas, Instituto Cajal, Madrid, Spain
Ana Covelo
Department of Neuroscience, University of Minnesota, Minneapolis, United States
Jesús J Ballesteros
Albacete Science and Technology Park, Institute for Research in Neurological Disabilities, University of Castilla-La Mancha, Albacete, Spain; Department of Neurophysiology, Faculty of Medicine, Ruhr University Bochum, Bochum, Germany
Laura Schlosser
Molecular Physiology, Center for Integrative Physiology and Molecular Medicine, University of Saarland, Homburg, Germany
Alicia Hernández-Vivanco
Consejo Superior de Investigaciones Científicas, Instituto Cajal, Madrid, Spain
Mario Martín-Fernández
Department of Neuroscience, University of Minnesota, Minneapolis, United States
Ruth Quintana
Department of Neuroscience, University of Minnesota, Minneapolis, United States
Abdelrahman Rayan
Department of Neurophysiology, Faculty of Medicine, Ruhr University Bochum, Bochum, Germany
Adolfo Díez
Department of Neuroscience, University of Minnesota, Minneapolis, United States
Marco Fuenzalida
Center of Neurobiology and Brain Plasticity, Institute of Physiology, Faculty of Science, Universidad de Valparaíso, Valparaiso, Chile
Interneurons are critical for proper neural network function and can activate Ca2+ signaling in astrocytes. However, the impact of the interneuron-astrocyte signaling into neuronal network operation remains unknown. Using the simplest hippocampal Astrocyte-Neuron network, i.e., GABAergic interneuron, pyramidal neuron, single CA3-CA1 glutamatergic synapse, and astrocytes, we found that interneuron-astrocyte signaling dynamically affected excitatory neurotransmission in an activity- and time-dependent manner, and determined the sign (inhibition vs potentiation) of the GABA-mediated effects. While synaptic inhibition was mediated by GABAA receptors, potentiation involved astrocyte GABAB receptors, astrocytic glutamate release, and presynaptic metabotropic glutamate receptors. Using conditional astrocyte-specific GABAB receptor (Gabbr1) knockout mice, we confirmed the glial source of the interneuron-induced potentiation, and demonstrated the involvement of astrocytes in hippocampal theta and gamma oscillations in vivo. Therefore, astrocytes decode interneuron activity and transform inhibitory into excitatory signals, contributing to the emergence of novel network properties resulting from the interneuron-astrocyte interplay.