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Savaglio, M. A.

Publications and source records attributed to Savaglio, M. A..

2 recordsLinked to original sources

Direction of motion decoding in mouse V1: Neuron predictive power relates to functional connectivity organization

Variability in single neuron responses presents a challenge in establishing reliable representations of visual stimuli essential for driving behavior. To enhance accuracy, integration of responses from multiple neurons is imperative. This study leverages simultaneous recordings from a large population (tens of hundreds) of neurons, achieved through in vivo mesoscopic 2-photon calcium imaging of the primary visual cortex (V1) in mice, under visual stimulus conditions as well as in resting state (absence of stimulus). The visual stimulus consisted of 16 distinct randomly shuffled directions of motion presented to the mice. We employed mutual information to identify neurons that contain the most significant information about the stimulus direction. As expected, neurons displaying high predictive power (HPP) in stimulus decoding exhibit elevated firing event rates during stimulus presentation. Furthermore, functional connectivity among HPP neurons during visual stimulation is denser and stronger compared to functional connectivity among other visually responsive neurons. Functional connections among HPP neurons appear to form independently of distance, suggesting a distributed yet highly coordinated network. In contrast, HPP neuronal activity and functional connectivity differed significantly at resting state. Specifically, during the resting state, HPP neurons exhibited lower event rates and functional connectivity structure that was not significantly different from that of other visually responsive neurons. This suggests that HPP neurons are less susceptible to being driven simultaneously by internal brain states in the absence of a stimulus. Finally, the tuning properties of HPP neurons were unexpectedly diverse: while some were sharply tuned, others conveyed a similar amount of mutual information, despite exhibiting much weaker tuning. This study sheds light on the organization of neuronal ensembles important for decoding visual motion direction in mouse area V1, contributing to the understanding of information processing in mouse visual cortex.

neuroscience↗

Brain orchestra under spontaneous conditions: Identifying communication modules from the functional architecture of area V1

While single-neuron responses in mouse V1 are well characterized, less is known about how functional ensembles-- groups of neurons that co-activate more frequently than expected by chance--emerge as computational units within laminar V1 circuits. Even with increasingly detailed knowledge of structural connectivity, the rules governing ensemble organization and interactions remain unclear. We imaged pyramidal neurons across granular (L4) and supragranular (L2/3) layers of mouse V1 and applied pairwise functional connectivity analysis to identify multi-neuronal ensembles as putative information-processing modules. In the absence of visual stimulation, 19-34% of pyramidal pairs within 300{micro}m were functionally connected, declining to 10% at 1 mm. Layer 2 to 4 laminar networks exhibited a small-world architecture, L4 displaying slightly denser connectivity and a near-uniform degree-of-connectivity distribution. We propose that neurons together with their first-order functionally connected (1FC) partners constitute putative elementary units of cortical computation. The firing probability of layer 2/3 neurons exhibits a ReLU-like nonlinearity, emerging when [≥] 13% of L4-1FC "putative inputs" co-fire, yielding sparse yet reliable responses. Moreover, L2/3 neuronal responses depend on the count (N), not the identity, of co-active L4-1FC partners, with response sensitivity scaling as a power law in N. These properties persist during visual stimulation and across different states of alertness. Interestingly, L2/3 neurons with L4-1FC modules of different sizes exhibit distinct coupling to brain-state and different computational signatures. This framework yields mechanistic insight into cortical circuit organization, complementary to structural connectivity, helping to link biological circuitry to deep-learning models of artificial intelligence.

neuroscience↗