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Bandi, A.

Publications and source records attributed to Bandi, A..

6 recordsLinked to original sources

Different state-dependence of population codes across cortex

During perceptual decision-making tasks, behavioral performance and its neural correlates vary with changes in internal states such as arousal, motivation, and strategy. It is not yet clear whether these state fluctuations differently impact the distributed neural processes that underlie task performance, from sensory processing to control of motor outputs. The posterior parietal cortex (PPC) is an association-level cortical region implicated in sensorimotor transformations, but evidence of its causal requirement in decision-making tasks has been contradictory. We trained mice to perform a navigation-based sound localization task and asked how natural fluctuations in behavioral state related to neural processing in association areas during decision-making. Behavioral performance in expert-level mice was not static but instead transitioned between periods of near-perfect performance and biased, less accurate performance. Using a hidden Markov model, we could reliably define these as distinct strategies that included a high-performance state where mice used relevant stimulus information to inform choices, and two biased states where mice weighted stimulus information less strongly. Optogenetic inactivation of PPC decreased task performance accuracy, and the model captured the resulting change in behavioral strategy as a reduction in the weighting of the auditory cues and an increase in behavioral bias, in predicting mices decisions. Two-photon calcium imaging revealed that performance states strongly influenced population activity patterns in PPC, but not primary auditory cortex (AC). Surprisingly, activity of individual PPC neurons was better explained by external inputs and behavioral variables during biased behavioral performance, while shared variability across neurons in PPC was strongest in the high-performance state. Together, these findings suggest that neural activity in parietal cortex is causally required for decisions and is linked to behavioral performance states.

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Pre-existing visual responses in a projection-defined dopamine population explain individual learning trajectories

Learning a new task is challenging because the world is high dimensional, with only a subset of features being reward-relevant. What neural mechanisms contribute to initial task acquisition, and why do some individuals learn a new task much more quickly than others? To address these questions, we recorded longitudinally from dopamine (DA) axon terminals in mice learning a visual task. Across striatum, DA responses tracked idiosyncratic and side-specific learning trajectories. However, even before any rewards were delivered, contralateral-side-specific visual responses were present in DA terminals only in the dorsomedial striatum (DMS). These pre-existing responses predicted the extent of learning for contralateral stimuli. Moreover, activation of these terminals improved contralateral performance. Thus, the initial conditions of a projection-specific and feature-specific DA signal help explain individual learning trajectories. More broadly, this work implies that functional heterogeneity across DA projections serves to bias target regions towards learning about different subsets of task features, providing a mechanism to address the dimensionality of the initial task learning problem.

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A neural substrate of sex-dependent modulation of motivation by value

While there is emerging evidence of sex differences in decision-making behavior, the neural substrates that underlie such differences remain largely unknown. Here, we demonstrate that in mice performing a value-based decision-making task, while choices are similar between the sexes, motivation to engage in the task is modulated by action value in females more strongly than in males. Inhibition of activity in anterior cingulate cortex (ACC) neurons that project to the dorsomedial striatum (DMS) disrupts this relationship between value and motivation preferentially in females, without affecting choice in either sex. In line with these effects, in females compared to males, ACC-DMS neurons have stronger representations of negative outcomes, and more neurons are active when the value of the chosen option is low. In contrast, the representation of each choice is similar between the sexes. Thus, we identify a neural substrate that contributes to sex-specific modulation of motivation by value.

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Strong and opponent contributions of dorsomedial striatal pathways to behavior depends on cognitive demands and task strategy

A classic view of the striatum holds that activity in direct and indirect pathways oppositely modulates motor output. Whether this involves direct control of movement, or reflects a cognitive process underlying movement, remains unresolved. Here we find that strong, opponent control of behavior by the two pathways of the dorsomedial striatum (DMS) depends on the cognitive requirements of a task. Furthermore, a latent state model (a hidden markov model with generalized linear model observations) reveals that--even within a single task--the contribution of the two pathways to behavior is state-dependent. Specifically, the two pathways have large contributions in one of two states associated with a strategy of evidence accumulation, compared to a state associated with a strategy of repeating previous choices. Thus, both the demands imposed by a task, as well as the internal state of mice when performing a task, determine whether DMS pathways provide strong and opponent control of behavior.

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A comparison of dopaminergic and cholinergic populations reveals unique contributions of VTA dopamine neurons to short-term memory

We systematically compared the contribution of two dopaminergic and two cholinergic ascending populations to a spatial short-term memory task in rats. In ventral tegmental area dopamine (VTA-DA) and nucleus basalis cholinergic (NB-ChAT) populations, trial-by-trial fluctuations in activity during the delay period related to performance with an inverted-U, despite the fact that both populations had low activity during that time. Transient manipulations revealed that only VTA-DA neurons, and not the other three populations we examined, contributed causally and selectively to short-term memory. This contribution was most significant during the delay period, when both increases or decreases in VTA-DA activity impaired short-term memory. Our results reveal a surprising dissociation between when VTA-DA neurons are most active and when they have the biggest causal contribution to short-term memory, while also providing new types of support for classic ideas about an inverted-U relationship between neuromodulation and cognition.

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Optogenetic and transcriptomic interrogation of enhanced muscle function in the paralyzed mouse whisker pad

The functional state of denervated muscle is a critical factor in the ability to restore movement after injury- or disease-related paralysis. Here we used peripheral optogenetic stimulation and transcriptome profiling in the mouse whisker system to investigate the time course of changes in neuromuscular function following complete unilateral facial nerve transection. While most skeletal muscles rapidly lose functionality after lower motor neuron denervation, optogenetic muscle stimulation of the paralyzed whisker pad revealed sustained increases in the sensitivity, velocity, and amplitude of whisker movements, and reduced fatigability, starting 48 h after denervation. RNA-seq analysis showed distinct regulation of multiple gene families in denervated whisker pad muscles compared to the atrophy-prone soleus, including prominent changes in ion channels and contractile fibers. Together, our results define the unique functional and transcriptomic landscape of denervated facial muscles, and have general implications for restoring movement after neuromuscular injury or disease. New & NoteworthyOptogenetic activation of muscle can be used to non-invasively induce movements and probe muscle function. We used this technique in mice to investigate changes in whisker movements following facial nerve transection. We found unexpectedly enhanced functional properties of whisker pad muscle following denervation, accompanied by unique transcriptomic changes. Our findings highlight the utility of the mouse whisker pad for investigating the restoration of movement after paralysis.

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