Cholinergic modulation of dentate gyrus processing through dynamic reconfiguration of inhibitory circuits
Mora B. Ogando,
Olivia Pedroncini,
Noel Federman,
Sebastián A. Romano,
Luciano A. Brum,
Guillermo M. Lanuza,
Damian Refojo,
Antonia Marin-Burgin
Affiliations
Mora B. Ogando
Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA) – CONICET - Partner Institute of the Max Planck Society Godoy Cruz 2390, C1425FQD Buenos Aires, Argentina; Corresponding author
Olivia Pedroncini
Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA) – CONICET - Partner Institute of the Max Planck Society Godoy Cruz 2390, C1425FQD Buenos Aires, Argentina
Noel Federman
Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA) – CONICET - Partner Institute of the Max Planck Society Godoy Cruz 2390, C1425FQD Buenos Aires, Argentina
Sebastián A. Romano
Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA) – CONICET - Partner Institute of the Max Planck Society Godoy Cruz 2390, C1425FQD Buenos Aires, Argentina
Luciano A. Brum
Fundación Instituto Leloir-Instituto de Investigaciones Bioquímicas de Buenos Aires-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Patricias Argentinas 435, Buenos Aires C1405BWE, Argentina
Guillermo M. Lanuza
Fundación Instituto Leloir-Instituto de Investigaciones Bioquímicas de Buenos Aires-Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Av. Patricias Argentinas 435, Buenos Aires C1405BWE, Argentina
Damian Refojo
Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA) – CONICET - Partner Institute of the Max Planck Society Godoy Cruz 2390, C1425FQD Buenos Aires, Argentina
Antonia Marin-Burgin
Instituto de Investigación en Biomedicina de Buenos Aires (IBioBA) – CONICET - Partner Institute of the Max Planck Society Godoy Cruz 2390, C1425FQD Buenos Aires, Argentina; Corresponding author
Summary: The dentate gyrus (DG) of the hippocampus plays a key role in memory formation, and it is known to be modulated by septal projections. By performing electrophysiology and optogenetics, we evaluated the role of cholinergic modulation in the processing of afferent inputs in the DG. We show that mature granule cells (GCs), but not adult-born immature neurons, have increased responses to afferent perforant path stimuli upon cholinergic modulation. This is due to a highly precise reconfiguration of inhibitory circuits, differentially affecting Parvalbumin and Somatostatin interneurons, resulting in a nicotinic-dependent perisomatic disinhibition of GCs. This circuit reorganization provides a mechanism by which mature GCs could escape the strong inhibition they receive, creating a window of opportunity for plasticity. Indeed, coincident activation of perforant path inputs with optogenetic release of acetylcholine produces a long-term potentiated response in GCs, essential for memory formation.