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Gonzalo Cogno, S.

Publications and source records attributed to Gonzalo Cogno, S..

2 recordsLinked to original sources

A common structure in recurrent networks supports neural sequence generation locally and in downstream neurons

Neural sequences, characterized by neurons or groups of neurons that fire one after the other, have been observed in multiple brain regions, across species, and are known to underlie a diversity of brain functions. To flexibly support behaviour and cognition, neural sequences exhibit much variability in properties like their temporal width, baseline, and peak firing rate. Despite this variability and the central role that sequences play in supporting brain function, a framework that explains how flexible sequences are generated and dynamically maintained within a circuit is still missing. Here we go beyond traditional approaches that investigate a one-to-one relationship between network connectivity and specific sequential dynamics. Instead, we train recurrent neural network models to generate a repertoire of sequential dynamics and characterize the obtained connectivity matrices. We found that different connectivity matrices can generate the same neural sequence, yet all connectivity matrices that generate a specific sequence share a common connectivity profile, defined here as the average weight between pairs of neurons as a function of their distance in the sequence ordering. It is the connectivity profile, as opposed to the connectivity matrix, that serves as a fingerprint of the sequential dynamics and shapes the network response to perturbations of the neural activity. Our model predictions were consistent with results obtained from experimental data recorded across brain regions and across species. Finally, we demonstrated that neural sequences can facilitate and constrain the formation of a large repertoire of sequences in downstream brain regions, with the potential of acting as scaffolds for a wide range of computations. Altogether, our results explain how network connectivity can generate a diversity of neural sequences across circuits and how those sequences can be flexibly adapted. Our framework reveals sequences as a common algorithm to support brain function across brain regions and species.

neuroscience↗

Minute-scale oscillatory sequences in medial entorhinal cortex

The medial entorhinal cortex (MEC) hosts many of the brains circuit elements for spatial navigation and episodic memory, operations that require neural activity to be organized across long durations of experience1. While location is known to be encoded by a plethora of spatially tuned cell types in this brain region2-6, little is known about how the activity of entorhinal cells is tied together over time. Among the brains most powerful mechanisms for neural coordination are network oscillations, which dynamically synchronize neural activity across circuit elements7-10. In MEC, theta and gamma oscillations provide temporal structure to the neural population activity at subsecond time scales1,11-13. It remains an open question, however, whether similarly powerful coordination occurs in MEC at behavioural time scales, in the second-to-minute regime. Here we show that MEC activity can be organized into a minute-scale oscillation that entrains nearly the entire cell population, with periods ranging from 10 to 100 seconds. Throughout this ultraslow oscillation, neural activity progresses in periodic and stereotyped sequences. This activity was elicited while mice ran at free pace on a rotating wheel in darkness, with no change in its location or running direction and no scheduled rewards. The oscillation sometimes advanced uninterruptedly for tens of minutes, transcending epochs of locomotion and immobility. Similar oscillatory sequences were not observed in neighboring parasubiculum or in visual cortex. The ultraslow oscillation of activity sequences in MEC may have the potential to couple its neurons and circuits across extended time scales and to serve as a scaffold for processes that unfold at behavioural time scales, such as navigation and episodic memory formation.

neuroscience↗