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Publication : Modulation of Coordinated Activity across Cortical Layers by Plasticity of Inhibitory Synapses.

First Author  Lourenço J Year  2020
Journal  Cell Rep Volume  30
Issue  3 Pages  630-641.e5
PubMed ID  31968242 Mgi Jnum  J:288105
Mgi Id  MGI:6415844 Doi  10.1016/j.celrep.2019.12.052
Citation  Lourenco J, et al. (2020) Modulation of Coordinated Activity across Cortical Layers by Plasticity of Inhibitory Synapses. Cell Rep 30(3):630-641.e5
abstractText  In the neocortex, synaptic inhibition shapes all forms of spontaneous and sensory evoked activity. Importantly, inhibitory transmission is highly plastic, but the functional role of inhibitory synaptic plasticity is unknown. In the mouse barrel cortex, activation of layer (L) 2/3 pyramidal neurons (PNs) elicits strong feedforward inhibition (FFI) onto L5 PNs. We find that FFI involving parvalbumin (PV)-expressing cells is strongly potentiated by postsynaptic PN burst firing. FFI plasticity modifies the PN excitation-to-inhibition (E/I) ratio, strongly modulates PN gain, and alters information transfer across cortical layers. Moreover, our LTPi-inducing protocol modifies firing of L5 PNs and alters the temporal association of PN spikes to gamma-oscillations both in vitro and in vivo. All of these effects are captured by unbalancing the E/I ratio in a feedforward inhibition circuit model. Altogether, our results indicate that activity-dependent modulation of perisomatic inhibitory strength effectively influences the participation of single principal cortical neurons to cognition-relevant network activity.
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