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Augusto, E.

Publications and source records attributed to Augusto, E..

5 recordsLinked to original sources

Adeno-associated virus delivered Cre recombinase as a versatile strategy for modeling focal neuronal lesions

Lesion studies remain central to neuroscience, offering key insights into brain-behavior relationships. Excitotoxic agents, though widely used, often produce inconsistent, non-specific, and ethically complex outcomes. In contrast, optogenetics and chemogenetics enable precise, reversible manipulations but pose technical and interpretational challenges, including cost and non-physiological activation. There remains a need for robust, controlled, and ethical lesion methods. Here, we present Cre recombinase expression as a reproducible alternative to excitotoxic lesions in mice. Using high titration adeno-associated viral (AAV) vectors, we show that Cre expression induces focal neurodegeneration across brain regions, affecting both excitatory and inhibitory neurons. This effect is independent of viral serotype or fluorescent tags and is not visible with standard staining but is revealed by neuronal markers. The resulting neuronal loss is followed by glial remodeling and significant behavioral alterations. AAV-mediated Cre expression thus provides a powerful, genetically targeted lesion model that bridges classical and modern approaches to circuit manipulation.

neuroscience↗

Secondary motor cortex tracks decision value and supports behavioral flexibility during non-instructed choice

Optimal decision-making relies on interconnected frontal brain regions, which permit animals to adapt their decisions based on their internal state, experience, and environmental context. Among them, the secondary motor cortex (M2) shows earlier decision-related activity required for sensory-guided action selection. However, the role of M2 in adaptive decision-making in the absence of instructive sensory cues remains unclear. Under such conditions, action-selection relies on abstract representations of actions and their values. Using in vivo microscopy and modeling, we showed that M2 neurons in mice exhibited persistent activity encoding decision values (DV) predicting the probability of action-selection during a non-cue-guided lever task. This was confirmed by the reduced reversal performance upon M2 optogenetic inhibition prior to action-selection. Furthermore, updates in DV determined the rate at which learning is reversed. Together, these results provide strong evidence of the use of DV by M2 to adapt choice in the absence of instructive sensory cues. Declaration of interestsThe authors declare no competing financial interests.

neuroscience↗

Facial expressions in mice reveal latent cognitive variables and their neural correlates

Brain activity controls adaptive behavior but also drives unintentional incidental movements. Such movements could thus potentially be used to read out internal cognitive variables also neurally computed. Establishing this, however, would require ruling out that incidental movements reflect cognition only because they are coupled with task-related responses through the biomechanics of the body. We addressed this issue in a foraging task for mice where multiple decision variables are simultaneously encoded even if, at any given time, only one of them is used. We found that characteristic features of the face simultaneously encode not only the currently used decision variables, but also independent and unexpressed ones, and we show that these features partially originate from neural activity in the secondary motor cortex. Our results suggest that the face reflects ongoing computations above and beyond those related to task demands, demonstrating the ability of noninvasive monitoring to expose otherwise latent cognitive states.

neuroscience↗

AMPAR trafficking dependent LTP initiates cortical remapping and adaptive behaviors during sensory experience

Cortical plasticity improves behaviors and helps recover lost functions after injury by adapting neuronal computations. However, the underlying synaptic and circuit mechanisms remain unclear. In mice, we found that trimming all but one whisker enhances sensory responses from the spared whisker in the somatosensory barrel cortex and occludes whisker-mediated long-term potentiation (w-LTP) in vivo. In addition, whisking-dependent behaviors that are initially impaired by single whisker experience (SWE) rapidly recover when associated cortical regions remap. Blocking the surface diffusion of AMPA receptors (AMPARs) suppresses the expression of w-LTP in naive mice with all whiskers intact, demonstrating that physiologically induced LTP in vivo requires AMPARs trafficking. We used this approach to demonstrate that w-LTP is required for SWE-mediated strengthening of synaptic inputs and initiates the recovery of previously learned skills during the early phases of SWE. Taken together, our data reveal that w-LTP mediates cortical remapping and behavioral improvement upon partial sensory deafferentation and demonstrates that restoration of sensory function after peripheral injury can be manipulated.

neuroscience↗

Non-linear dendritic integration in frontal circuits shapes sensory discrimination in rodents

Survival depends on the ability of animals to select the appropriate behavior in response to threat and safety sensory cues. However, the synaptic and circuit mechanisms by which the brain learns to encode accurate predictors of threat and safety remain largely unexplored. Here, we show that frontal association cortex (FrA) pyramidal neurons integrate auditory cues and basolateral amygdala (BLA) inputs non-linearly in a NMDAR-dependent manner. We found that the response of FrA pyramidal neurons was more pronounced to Gaussian noise than to pure 8 kHz tone, and that the activation of BLA-to-FrA axons was the strongest during safe periods in between conditioning pairings. Blocking BLA-to-FrA signaling specifically at the time of presentation of Gaussian noise (but not 8 kHz tone) as a safety signal impaired the formation of auditory fear memories. Taken together, our data reveal a circuit mechanism that facilitates the formation of fear traces in the FrA, thus providing a new framework for probing discriminative learning and related disorders.

neuroscience↗