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

Neuron

Volumn 93, Issue 2, 2017, Pages 299-307

  Storchi, Riccardo ^a   Bedford, Robert A ^a   Martial, Franck P ^a   Allen, Annette E ^a   Wynne, Jonathan ^a   Montemurro, Marcelo A ^a   Petersen, Rasmus S ^a   Lucas, Robert J ^a  

^a UNIVERSITY OF MANCHESTER   (United Kingdom)

Author keywords

dorsal lateral geniculate nucleus; freely moving extracellular recordings; intrinsically photosensitive retinal ganglion cells; irradiance; melanopsin; metameric light stimuli; narrowband gamma oscillations; neural population coding; receptor silent substitution; retina

Indexed keywords

MELANOPSIN; SCOTOPSIN;

ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; LATERAL GENICULATE BODY; LIGHT INTENSITY; LIGHT IRRADIANCE; MOUSE; NARROWBAND OSCILLATION; NEUROMODULATION; NONHUMAN; OSCILLATION; PHOTORECEPTOR; RETINA; SENSE OF COHERENCE; SIGNAL TRANSDUCTION; SPECTRAL SENSITIVITY; SUNLIGHT; ANIMAL; ELECTRORETINOGRAPHY; GAMMA RHYTHM; GENETICS; GENICULATE BODY; KNOCKOUT MOUSE; LIGHT; PHOTOSTIMULATION; PHYSIOLOGY; RETINA GANGLION CELL; VISION; VISUAL SYSTEM; WAKEFULNESS;

ANIMALS; ELECTRORETINOGRAPHY; GAMMA RHYTHM; GENICULATE BODIES; LIGHT; MICE; MICE, KNOCKOUT; PHOTIC STIMULATION; RETINA; RETINAL GANGLION CELLS; ROD OPSINS; VISION, OCULAR; VISUAL PATHWAYS; WAKEFULNESS;

EID: 85010301124     PISSN: 08966273     EISSN: 10974199     Source Type: Journal    
DOI: 10.1016/j.neuron.2016.12.027     Document Type: Article

References (32)

1. Allen, A.E., Storchi, R., Martial, F.P., Petersen, R.S., Montemurro, M.A., Brown, T.M., Lucas, R.J., Melanopsin-driven light adaptation in mouse vision. Curr. Biol. 24 (2014), 2481–2490.
2. Attwell, D., Laughlin, S.B., An energy budget for signaling in the grey matter of the brain. J. Cereb. Blood Flow Metab. 21 (2001), 1133–1145.
3. Averbeck, B.B., Latham, P.E., Pouget, A., Neural correlations, population coding and computation. Nat. Rev. Neurosci. 7 (2006), 358–366.
4. Barlow, H.B., Levick, W.R., Changes in the maintained discharge with adaptation level in the cat retina. J. Physiol. 202 (1969), 699–718.
5. Barlow, H.B., Fitzhugh, R., Kuffler, S.W., Change of organization in the receptive fields of the cat's retina during dark adaptation. J. Physiol. 137 (1957), 338–354.
6. Bisti, S., Clement, R., Maffei, L., Mecacci, L., Spatial frequency and orientation tuning curves of visual neurones in the cat: effects of mean luminance. Exp. Brain Res. 27 (1977), 335–345.
7. Brown, T.M., Gias, C., Hatori, M., Keding, S.R., Semo, M., Coffey, P.J., Gigg, J., Piggins, H.D., Panda, S., Lucas, R.J., Melanopsin contributions to irradiance coding in the thalamo-cortical visual system. PLoS Biol., 8, 2010, e1000558.
8. Castelo-Branco, M., Neuenschwander, S., Singer, W., Synchronization of visual responses between the cortex, lateral geniculate nucleus, and retina in the anesthetized cat. J. Neurosci. 18 (1998), 6395–6410.
9. Farrow, K., Teixeira, M., Szikra, T., Viney, T.J., Balint, K., Yonehara, K., Roska, B., Ambient illumination toggles a neuronal circuit switch in the retina and visual perception at cone threshold. Neuron 78 (2013), 325–338.
10. Fries, P., A mechanism for cognitive dynamics: neuronal communication through neuronal coherence. Trends Cogn. Sci. 9 (2005), 474–480.
11. Gray, C.M., König, P., Engel, A.K., Singer, W., Oscillatory responses in cat visual cortex exhibit inter-columnar synchronization which reflects global stimulus properties. Nature 338 (1989), 334–337.
12. Grimes, W.N., Schwartz, G.W., Rieke, F., The synaptic and circuit mechanisms underlying a change in spatial encoding in the retina. Neuron 82 (2014), 460–473.
13. Hankins, M.W., Lucas, R.J., The primary visual pathway in humans is regulated according to long-term light exposure through the action of a nonclassical photopigment. Curr. Biol. 12 (2002), 191–198.
14. Hoppensteadt, F.C., Izhikevich, E.M., Thalamo-cortical interactions modeled by weakly connected oscillators: could the brain use FM radio principles?. Biosystems 48 (1998), 85–94.
15. Kann, O., The energy demand of fast neuronal network oscillations: insights from brain slice preparations. Front. Pharmacol., 2, 2012, 90.
16. Kenyon, G.T., Moore, B., Jeffs, J., Denning, K.S., Stephens, G.J., Travis, B.J., George, J.S., Theiler, J., Marshak, D.W., A model of high-frequency oscillatory potentials in retinal ganglion cells. Vis. Neurosci. 20 (2003), 465–480.
17. Koepsell, K., Wang, X., Vaingankar, V., Wei, Y., Wang, Q., Rathbun, D.L., Usrey, W.M., Hirsch, J.A., Sommer, F.T., Retinal oscillations carry visual information to cortex. Front. Syst. Neurosci., 3, 2009, 4.
18. Lucas, R.J., Hattar, S., Takao, M., Berson, D.M., Foster, R.G., Yau, K.W., Diminished pupillary light reflex at high irradiances in melanopsin-knockout mice. Science 299 (2003), 245–247.
19. Müller, L.P.D., Do, M.T.H., Yau, K.W., He, S., Baldridge, W.H., Tracer coupling of intrinsically photosensitive retinal ganglion cells to amacrine cells in the mouse retina. J. Comp. Neurol. 518 (2010), 4813–4824.
20. Neuenschwander, S., Singer, W., Long-range synchronization of oscillatory light responses in the cat retina and lateral geniculate nucleus. Nature 379 (1996), 728–732.
21. Niell, C.M., Stryker, M.P., Modulation of visual responses by behavioral state in mouse visual cortex. Neuron 65 (2010), 472–479.
22. Odermatt, B., Nikolaev, A., Lagnado, L., Encoding of luminance and contrast by linear and nonlinear synapses in the retina. Neuron 73 (2012), 758–773.
23. Pedroarena, C., Llinás, R., Dendritic calcium conductances generate high-frequency oscillation in thalamocortical neurons. Proc. Natl. Acad. Sci. USA 94 (1997), 724–728.
24. Reifler, A.N.N., Chervenak, A.P., Dolikian, M.E., Benenati, B.A., Li, B.Y., Wachter, R.D., Lynch, A.M., Demertzis, Z.D., Meyers, B.S., Abufarha, F.S., et al. All spiking, sustained ON displaced amacrine cells receive gap-junction input from melanopsin ganglion cells. Curr. Biol. 25 (2015), 2763–2773.
25. Rhodes, P.A., Llinás, R., A model of thalamocortical relay cells. J. Physiol. 565 (2005), 765–781.
26. Sillito, A.M., Jones, H.E., Gerstein, G.L., West, D.C., Feature-linked synchronization of thalamic relay cell firing induced by feedback from the visual cortex. Nature 369 (1994), 479–482.
27. Storchi, R., Milosavljevic, N., Eleftheriou, C.G., Martial, F.P., Orlowska-Feuer, P., Bedford, R.A., Brown, T.M., Montemurro, M.A., Petersen, R.S., Lucas, R.J., Melanopsin-driven increases in maintained activity enhance thalamic visual response reliability across a simulated dawn. Proc. Natl. Acad. Sci. USA 112 (2015), E5734–E5743.
28. Tikidji-Hamburyan, A., Reinhard, K., Seitter, H., Hovhannisyan, A., Procyk, C.A., Allen, A.E., Schenk, M., Lucas, R.J., Münch, T.A., Retinal output changes qualitatively with every change in ambient illuminance. Nat. Neurosci. 18 (2015), 66–74.
29. Wachtmeister, L., Oscillatory potentials in the retina: what do they reveal. Prog. Retin. Eye Res. 17 (1998), 485–521.
30. Wong, K.Y., A retinal ganglion cell that can signal irradiance continuously for 10 hours. J. Neurosci. 32 (2012), 11478–11485.
31. Zhang, D.Q., Wong, K.Y., Sollars, P.J., Berson, D.M., Pickard, G.E., McMahon, D.G., Intraretinal signaling by ganglion cell photoreceptors to dopaminergic amacrine neurons. Proc. Natl. Acad. Sci. USA 105 (2008), 14181–14186.
32. Zohary, E., Shadlen, M.N., Newsome, W.T., Correlated neuronal discharge rate and its implications for psychophysical performance. Nature 370 (1994), 140–143.