Abstract

The establishment of precise neuronal connectivity during development is critical for sensing the external environment and informing appropriate behavioral responses. In the visual system, many connections are organized topographically, which preserves the spatial order of the visual scene. The superior colliculus (SC) is a midbrain nucleus that integrates visual inputs from the retina and primary visual cortex (V1) to regulate goal-directed eye movements. In the SC, topographically organized inputs from the retina and V1 must be aligned to facilitate integration. Previously, we showed that retinal input instructs the alignment of V1 inputs in the SC in a manner dependent on spontaneous neuronal activity; however, the mechanism of activity-dependent instruction remains unclear. To begin to address this gap, we developed two novel computational models of visual map alignment in the SC that incorporate distinct activity-dependent components. First, a Correlational Model assumes that V1 inputs achieve alignment with established retinal inputs through simple correlative firing mechanisms. A second Integrational Model assumes that V1 inputs contribute to the firing of SC neurons during alignment. Both models accurately replicate in vivo findings in wild type, transgenic and combination mutant mouse models, suggesting either activity-dependent mechanism is plausible. In silico experiments reveal distinct behaviors in response to weakening retinal drive, providing insight into the nature of the system governing map alignment depending on the activity-dependent strategy utilized. Overall, we describe novel computational frameworks of visual map alignment that accurately model many aspects of the in vivo process and propose experiments to test them.

Highlights

  • Processing sensory information is a critical task of the central nervous system, requiring the establishment of precisely ordered synaptic connectivity during development

  • In the present study we develop two novel models of visual map alignment in the superior colliculus (SC), focusing on the projection from V1 to the SC, which develops during the second postnatal week in mice [23]

  • We assume that retinocollicular and retino-geniculo-cortical connections have been established during the first postnatal week [33,34,35], i.e. topography has been established by retinal ganglion cells (RGCs) in the SC, and V1 neurons are projecting axons from a topographically ordered region (Fig 1)

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Summary

Introduction

Processing sensory information is a critical task of the central nervous system, requiring the establishment of precisely ordered synaptic connectivity during development. The development of topographic connections in the visual system has been the focus of intense study, both experimentally and theoretically, elucidating general principles underlying neural circuit wiring [3, 4]. These studies have focused primarily on the mechanisms by which topographic connectivity is established for a single projection. Little is known about the mechanisms by which topographic maps of space are aligned in these regions, in part due to a lack of computational frameworks that model this process

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