Modulation of Fast Narrowband Oscillations in the Mouse Retina and dLGN According to Background Light Intensity

Background light intensity (irradiance) substantially impacts the visual code in the early visual system at synaptic and single-neuron levels, but its influence on population activity is largely unexplored. We show that fast narrowband oscillations, an important feature of population activity, syste...

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Published inNeuron (Cambridge, Mass.) Vol. 93; no. 2; pp. 299 - 307
Main Authors Storchi, Riccardo, Bedford, Robert A., Martial, Franck P., Allen, Annette E., Wynne, Jonathan, Montemurro, Marcelo A., Petersen, Rasmus S., Lucas, Robert J.
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 18.01.2017
Elsevier Limited
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Abstract Background light intensity (irradiance) substantially impacts the visual code in the early visual system at synaptic and single-neuron levels, but its influence on population activity is largely unexplored. We show that fast narrowband oscillations, an important feature of population activity, systematically increase in amplitude as a function of irradiance in both anesthetized and awake, freely moving mice and at the level of the retina and dorsal lateral geniculate nucleus (dLGN). Narrowband coherence increases with irradiance across large areas of the dLGN, but especially for neighboring units. The spectral sensitivity of these effects and their substantial reduction in melanopsin knockout animals indicate a contribution from inner retinal photoreceptors. At bright backgrounds, narrowband coherence allows pooling of single-unit responses to become a viable strategy for enhancing visual signals within its frequency range. •Narrowband oscillation amplitude in retina and dLGN is largely defined by irradiance•At high irradiances, control of oscillations originates with melanopsin photoreception•Daylight irradiance monotonically increases narrowband coherence•Narrowband coherence amplifies visual responses within its frequency range Storchi et al. find that daylight irradiance, through melanopsin, systematically modulates amplitude of narrowband oscillations in mouse retina and dLGN and boosts visual signaling.
AbstractList Background light intensity (irradiance) substantially impacts the visual code in the early visual system at synaptic and single-neuron levels, but its influence on population activity is largely unexplored. We show that fast narrowband oscillations, an important feature of population activity, systematically increase in amplitude as a function of irradiance in both anesthetized and awake, freely moving mice and at the level of the retina and dorsal lateral geniculate nucleus (dLGN). Narrowband coherence increases with irradiance across large areas of the dLGN, but especially for neighboring units. The spectral sensitivity of these effects and their substantial reduction in melanopsin knockout animals indicate a contribution from inner retinal photoreceptors. At bright backgrounds, narrowband coherence allows pooling of single-unit responses to become a viable strategy for enhancing visual signals within its frequency range. •Narrowband oscillation amplitude in retina and dLGN is largely defined by irradiance•At high irradiances, control of oscillations originates with melanopsin photoreception•Daylight irradiance monotonically increases narrowband coherence•Narrowband coherence amplifies visual responses within its frequency range Storchi et al. find that daylight irradiance, through melanopsin, systematically modulates amplitude of narrowband oscillations in mouse retina and dLGN and boosts visual signaling.
Background light intensity (irradiance) substantially impacts the visual code in the early visual system at synaptic and single-neuron levels, but its influence on population activity is largely unexplored. We show that fast narrowband oscillations, an important feature of population activity, systematically increase in amplitude as a function of irradiance in both anesthetized and awake, freely moving mice and at the level of the retina and dorsal lateral geniculate nucleus (dLGN). Narrowband coherence increases with irradiance across large areas of the dLGN, but especially for neighboring units. The spectral sensitivity of these effects and their substantial reduction in melanopsin knockout animals indicate a contribution from inner retinal photoreceptors. At bright backgrounds, narrowband coherence allows pooling of single-unit responses to become a viable strategy for enhancing visual signals within its frequency range.
Author Storchi, Riccardo
Martial, Franck P.
Montemurro, Marcelo A.
Bedford, Robert A.
Allen, Annette E.
Wynne, Jonathan
Petersen, Rasmus S.
Lucas, Robert J.
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  surname: Martial
  fullname: Martial, Franck P.
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  surname: Allen
  fullname: Allen, Annette E.
  organization: Faculty of Life Sciences, University of Manchester, M13 9PT Manchester, UK
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  givenname: Jonathan
  surname: Wynne
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Issue 2
Keywords melanopsin
intrinsically photosensitive retinal ganglion cells
dorsal lateral geniculate nucleus
retina
metameric light stimuli
neural population coding
receptor silent substitution
irradiance
freely moving extracellular recordings
narrowband gamma oscillations
Language English
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Snippet Background light intensity (irradiance) substantially impacts the visual code in the early visual system at synaptic and single-neuron levels, but its...
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SubjectTerms Anesthesia
Animals
dorsal lateral geniculate nucleus
Electroretinography
freely moving extracellular recordings
Gamma Rhythm
Geniculate Bodies - physiology
intrinsically photosensitive retinal ganglion cells
irradiance
Light
melanopsin
metameric light stimuli
Mice
Mice, Knockout
narrowband gamma oscillations
neural population coding
Noise
Photic Stimulation
receptor silent substitution
Retina
Retina - physiology
Retinal Ganglion Cells - physiology
Rod Opsins - genetics
Vision, Ocular - physiology
Visual Pathways
Wakefulness
Title Modulation of Fast Narrowband Oscillations in the Mouse Retina and dLGN According to Background Light Intensity
URI https://dx.doi.org/10.1016/j.neuron.2016.12.027
https://www.ncbi.nlm.nih.gov/pubmed/28103478
https://www.proquest.com/docview/1861146149
https://search.proquest.com/docview/1861581775
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