Abstract

Although the ability to integrate information across the senses is compromised in some individuals for unknown reasons, similar defects have been observed when animals are reared without multisensory experience. The experience-dependent development of multisensory integration has been studied most extensively using the visual-auditory neuron of the cat superior colliculus (SC) as a neural model. In the normally-developed adult, SC neurons react to concordant visual-auditory stimuli by integrating their inputs in real-time to produce non-linearly amplified multisensory responses. However, when prevented from gathering visual-auditory experience, their multisensory responses are no more robust than their responses to the individual component stimuli. The mechanisms operating in this defective state are poorly understood. Here we examined the responses of SC neurons in “naïve” (i.e., dark-reared) and “neurotypic” (i.e., normally-reared) animals on a millisecond-by-millisecond basis to determine whether multisensory experience changes the operation by which unisensory signals are converted into multisensory outputs (the “multisensory transform”), or whether it changes the dynamics of the unisensory inputs to that transform (e.g., their synchronization and/or alignment). The results reveal that the major impact of experience was on the multisensory transform itself. Whereas neurotypic multisensory responses exhibited non-linear amplification near their onset followed by linear amplification thereafter, the naive responses showed no integration in the initial phase of the response and a computation consistent with competition in its later phases. The results suggest that multisensory experience creates an entirely new computation by which convergent unisensory inputs are used cooperatively to enhance the physiological salience of cross-modal events and thereby facilitate normal perception and behavior.

Highlights

  • A major issue of interest in sensory processing is how the brain develops the ability to use its different senses synergistically to enhance perception and behavior (Stein and Meredith, 1993; Murray and Wallace, 2012; Stein, 2012)

  • The darkreared sample showed a tight correlation between the multisensory and summed unisensory response dynamics (0–200 ms after Estimated Time of Convergence’ (ETOC): mean R2 = 0.67, p < 0.001 for all 1 ms steps) that was even stronger (p < 0.001, Wilcoxon signed-rank test)

  • The correlation in the unisensory and multisensory dynamics observed in the dark-reared cohort suggests that, as in the neurotypic cohort, unisensory inputs are being continuously synthesized into multisensory outputs; i.e., both signals are received and processed by the target neuron

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Summary

Introduction

A major issue of interest in sensory processing is how the brain develops the ability to use its different senses synergistically to enhance perception and behavior (Stein and Meredith, 1993; Murray and Wallace, 2012; Stein, 2012) This process of “multisensory integration” is ubiquitous, automatic, and effortless despite the complexity involved in coordinating the action of Experience Creates Multisensory Transform SC senses that have very different operational dynamics. Individual SC neurons generate amplified responses to spatiotemporally concordant visual-auditory stimuli (Meredith and Stein, 1986a; Wallace et al, 1998; Rowland et al, 2007), which are often derived from the same event (Parise et al, 2012; Kayser and Shams, 2015) This increases the physiological salience of the initiating event and the brain’s ability to organize appropriate behavioral responses to it. The specific neuronal mechanisms by which multisensory experience changes the neural circuit to achieve normal functional outcomes are unknown

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