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Fino, E.

Publications and source records attributed to Fino, E..

4 recordsLinked to original sources

Clustered and diffuse sensory corticostriatal wirings define complementary interneuron circuits

In the striatum, interneurons tightly control the activity of output neurons, the striatal projection neurons (SPN). Among these striatal interneurons, parvalbumin-expressing (PV) and somatostatin-expressing (SOM) cells exhibit markedly distinct electrophysiological and anatomical properties, suggesting differential integration into striatal circuits and distinct forms of feedforward inhibition onto SPN. However, it remains unclear whether differences already emerge at the level of corticostriatal connectivity and if they shape specific interactions with cortical inputs to SPN. Here, we investigated the spatial organization of the projections from the primary and secondary somatosensory areas (S1 and S2), onto striatal PV and SOM interneurons and SPN. With a combination of anatomical tracing and functional circuit mapping, we characterized key features of corticostriatal connectivity, including input number, origin, spacing, overlap and strength. We found that input spacing and strength, at both the individual cell and population levels, were the principal features distinguishing PV and SOM interneurons. In contrast, connectivity differed primarily in input number and laminar organization across S1 and S2. Our findings suggest two potential modes of interaction between interneurons and SPN connectivity: one in which PV interneurons receive S1 inputs structured in large clusters, that densely overlap with those of neighboring SPN, providing an anatomical substrate for potential neuronal assemblies. And another in which SOM interneurons also receive abundant cortical inputs, but thinly disseminated across S1 and S2 and that overlap little with those of SPN, potentially shaping these cell integration through input cross-interaction. These cell-type principles of corticostriatal wiring may support distinct forms of striatal computation.

neuroscience↗

Early alterations of motor learning and corticostriatal network activity in a Huntington's disease mouse model

Huntingtons disease (HD) is a neurodegenerative disorder that presents motor, cognitive and psychiatric symptoms as it progresses. Prior to motor symptoms onset, alterations and dysfunctions in the corticostriatal projections have been described along with cognitive deficits, but the sequence of early defects of brain circuits is largely unknown. There is thus a crucial need to identify early alterations that precede symptoms and that could be used as potential early disease markers. Using an HD knock-In mouse model (HdhCAG140/+) that recapitulates the human genetic alterations and that show a late and progressive appearance of anatomical and behavior deficits, we identified early alterations in the motor learning abilities of young mice, long before any motor coordination defects. In parallel, ex vivo two-photon calcium recordings revealed that young HD mice have altered basal activity patterns in both dorsomedial and dorsolateral parts of the striatum. In addition, while wild-type mice display specific reorganization of the activity upon motor training, network alterations present in the basal state of non-trained mice are not affected by motor training of HD mice. Our results thus identify early behavioral deficits and network alterations that could serve as early markers of the disease.

neuroscience↗

Somatostatin interneurons select dorsomedial striatal representations of the initial learning phase

The dorsomedial striatum (DMS) is an associative node involved in the adaptation of ongoing actions to the environmental context and in the initial formation of motor sequences. In early associative or motor learning phases, DMS activity shows a global decrease in neuron firing, eventually giving rise to a select group of active cells, whose number is correlated with animal performance. Unveiling how those representation emerge from DMS circuits is crucial for understanding plasticity mechanisms of early adjustments to learning a task. Here, we hypothesized that inhibitory microcircuits formed by local interneurons are responsible for the genesis of early DMS representation and associated task performance. Despite the low density of somatostatin (SOM)-positive cells, we observed that selective manipulation of SOM cells disrupted reorganization of DMS activity and modulated initial phases of learning in two behavioral contexts. This effect was cell-specific as manipulation of parvalbumin-positive interneurons had no significant effect. Finally, we identified the high plasticity of SOM innervation in the DMS as a key modulator of the SPN excitability and firing activity. Hence, SOM interneurons set the pace of early learning by actively controlling the remapping of DMS network activity.

neuroscience↗

Reading of ingroup politicians smiles triggers smiling in the corner of ones eyes

Capturing political support from spontaneous smile reactions detected in others faces can be used to gauge electorate preference. But will a smile elicited in the corner of ones eye while reading of a favored politician smiling indicate positive disposition and political support for target candidates? From an embodied simulation perspective, we tested whether reading of an ingroup or outgroup politician smiling would trigger morphologically different smiles in faces of readers. In a reading task in the laboratory, participants were presented with subject-verb phrases describing left and right-wing politicians smiling or frowning while their facial muscular reactions were measured via electromyography (EMG) recording from the zygomaticus major (ZM, lip puller muscle), orbicularis oculi (OO, eye corner muscle) and the corrugator supercili (CS, wrinkler of the eyebrows). We expected and found that participants responded with a smile detected at the lip puller (ZM) and eye corner (OO) facial muscles when exposed to portrayals of smiling politicians of same political orientation, and reported more positive emotions towards these latter. When reading about outgroup politicians smiling, there was a weaker activation of the lip corner (ZM) muscle and no activation of the eye corner (OO) muscle, while emotions reported towards outgroup politicians were significantly more negative. Also, a more enhanced frown response (CS) was found for ingroup compared to outgroup politicians frown expressions. Present findings suggest that a politicians smile may go a long way to influence electorates through both non-verbal and verbal pathways. They add another layer to our understanding of how language and social information shape embodied effects in a highly nuanced manner.

physiology↗