Visual map development depends on the temporal pattern of binocular activity in mice

Nat Neurosci. 2011 Nov 18;15(2):298-307. doi: 10.1038/nn.3007.

Abstract

Binocular competition is thought to drive eye-specific segregation in the developing visual system, potentially through Hebbian synaptic learning rules that are sensitive to correlations in afferent activity. Altering retinal activity can disrupt eye-specific segregation, but little is known about the temporal features of binocular activity that modulate visual map development. We used optogenetic techniques to directly manipulate retinal activity in vivo and identified a critical period before eye opening in mice when specific binocular features of retinal activity drive visual map development. Synchronous activation of both eyes disrupted segregation, whereas asynchronous stimulation enhanced segregation. The optogenetic stimulus applied was spatially homogenous; accordingly, retinotopy of ipsilateral projections was markedly perturbed, but contralateral retinotopy was unaffected or even improved. These results provide direct evidence that the synchrony and precise temporal pattern of binocular retinal activity during a critical period in development regulates eye-specific segregation and retinotopy in the developing visual system.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Action Potentials / genetics
  • Animals
  • Animals, Newborn
  • Brain Mapping*
  • Calcium / metabolism
  • Channelrhodopsins
  • Critical Period, Psychological*
  • Functional Laterality
  • In Vitro Techniques
  • Light
  • Luminescent Proteins / genetics
  • Mice
  • Mice, Inbred C57BL
  • Mice, Transgenic
  • Neuronal Plasticity / genetics
  • Patch-Clamp Techniques
  • Receptors, Nicotinic / deficiency
  • Receptors, Nicotinic / genetics
  • Retina / cytology
  • Retinal Ganglion Cells / physiology
  • Superior Colliculi / physiology
  • Time Factors
  • Vision, Binocular / genetics
  • Vision, Binocular / physiology*
  • Visual Pathways / physiology*

Substances

  • Channelrhodopsins
  • Luminescent Proteins
  • Receptors, Nicotinic
  • nicotinic receptor beta2
  • Calcium