Sleep and plasticity in the visual cortex: more than meets the eye

Current Opinion in Neurobiology

Volumn 44, Issue , 2017, Pages 8-12

  Frank, Marcos G ^a  

^a WASHINGTON STATE UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

BINOCULAR VISION; BRAIN DEVELOPMENT; BRAIN FUNCTION; EYE DOMINANCE; HOMEOSTASIS; HUMAN; LONG TERM POTENTIATION; MOLECULAR BIOLOGY; MONOCULAR VISION; NERVE CELL PLASTICITY; NEUROANATOMY; NEUROMODULATION; NEUROPHYSIOLOGY; NONHUMAN; REM SLEEP; REVIEW; SLEEP; SLEEP PARAMETERS; SYNAPTIC TRANSMISSION; VISUAL CORTEX; VISUAL NERVOUS SYSTEM; VISUAL STIMULATION; WAKEFULNESS; PHYSIOLOGY;

HUMANS; NEURONAL PLASTICITY; SLEEP; VISUAL CORTEX;

EID: 85010040342     PISSN: 09594388     EISSN: 18736882     Source Type: Journal    
DOI: 10.1016/j.conb.2017.01.001     Document Type: Review

References (43)

1. 1 Smith, G.B., Heynen, A.J., Bear, M.F., Bidirectional synaptic mechanisms of ocular dominance plasticity in visual cortex. Philos Trans R Soc B Biol Sci 364 (2009), 357–367.
2. 2 Espinosa, J.S., Stryker, M.P., Development and plasticity of the primary visual cortex. Neuron 75 (2012), 230–249.
3. 3 Crair, M.C., Shah, R.D., Long-term potentiation and long-term depression in experience-dependent plasticity. Â Â Larry R.S, (eds.) Encyclopedia of Neuroscience, 2009, Academic Press, 561–570.
4. 4 Pettigrew, J.D., Garey, L.J., Selective modification of single neuron properties in the visual cortex of kittens. Brain Res 66 (1974), 160–164.
5. 5 Peck, C.K., Blakemore, C., Modification of single neurons in the kitten's visual cortex after brief periods of monocular deprivation. Exp Brain Res 22 (1975), 57–68.
6. 6 Ramachandran, V.S., Ary, M., Evidence for a consolidation effect during changes in ocular dominance of cortical neurons in kittens. Behav Neural Biol 35 (1982), 211–216.
7. 7 Rauschecker, J.P., Hahn, S., Ketamine-Xylazine anesthesia blocks consolidation of ocular dominance changes in kitten visual cortex. Nature 326 (1987), 183–185.
8. 8 Mioche, L., Singer, W., Chronic recordings from single sites of kitten striate cortex during experience-dependent modifications of receptive-field properties. J Neurophysiol 62 (1989), 185–197.
9. 9 Roffwarg, H.P., Muzio, J.N., Dement, W.C., Ontogenetic development of the human sleep-dream cycle. Science, 1966, 604–619.
10. 10 Jouvet-Mounier, D., Astic, L., Lacote, D., Ontogenesis of the states of sleep in rat, cat and guinea pig during the first postnatal month. Dev Psychobiol 2 (1970), 216–239.
11. 11 Valatx, J.L., Jouvet, D., Jouvet, M., Evolution electroencephalographique des differents etats de sommeil chez le chaton. Electroencephalogr Clin Neurophysiol 17 (1964), 218–233.
12. 12 Pompeiano, O., Pompeiano, M., Corvaja, N., Effects of sleep deprivation on the postnatal development of visual-deprived cells in the cat's lateral geniculate nucleus. Arch Ital Biol 134 (1995), 121–140.
13. 13 Oksenberg, A., Shaffery, J.P., Marks, G.A., Speciale, S.G., Mihailoff, G., Roffwarg, H.P., Rapid eye movement sleep deprivation in kittens amplifies LGN cell-size disparity induced by monocular deprivation. Dev Brain Res 97 (1996), 51–61.
14. 14 Shaffery, J.P., Roffwarg, H.P., Speciale, S.G., Marks, G.A., Ponto-geniculo-occipital wave suppression amplifies lateral geniculate nuclues cell-size changes in monocularly deprived kittens. Dev Brain Res 114 (1999), 109–119.
15. 15 Shaffery, J.P., Sinton, C.M., Bissette, G., Roffwarg, H.P., Marks, G.A., Rapid eye movement sleep deprivation modifies expression of long-term potentiation in visual cortex of immature rats. Neuroscience 110 (2002), 431–443.
16. 16 Freeman, R.D., Olson, C.R., Is there a ‘consolidation’ effect for monocular deprivation?. Nature 282 (1979), 404–406.
17. 17 Frank, M.G., Sleep and developmental brain plasticity: not just for kids. Prog Brain Res 193 (2011), 221–232.
18. 18 Frank, M.G., Stryker, M.P., The role of sleep in the development of central visual pathways. Maquet, P., Smith, C., Stickgold, R., (eds.) Sleep and Brain Plasticity, 2003, Oxford University Press, 189–206.
19. 19 Frank, M.G., Issa, N.P., Stryker, M.P., Sleep enhances plasticity in the developing visual cortex. Neuron 30 (2001), 275–287.
20. 20•• Dumoulin Bridi, M., Aton, S.J., Seibt, J., Renouard, L., Coleman, T., Frank, M.G., Rapid eye movement sleep promotes cortical plasticity in the developing brain. Sci Adv 1 (2015), 1–8 This study demonstrated a crucial role for REM sleep in ocular dominance plasticity.
21. 21 Daw, N.W., Sato, H., Fox, K., Carmichael, T., Gingerich, R., Cortisol reduces plasticity in the kitten visual cortex. J Neurobiol 22 (1991), 158–168.
22. 22 Jha, S.K., Jones, B.E., Coleman, T., Steinmetz, N., Law, C., Griffin, G., Hawk, J., Frank, M.G., Sleep-dependent plasticity requires cortical activity. J Neurosci 25 (2005), 9266–9274.
23. 23 Frank, M.G., Jha, S.K., Coleman, T., Blockade of postsynaptic activity in sleep inhibits developmental plasticity in visual cortex. Neuroreport 17 (2006), 1459–1463.
24. 24 Aton, S.J., Seibt, J., Dumoulin, M., Jha, S.K., Steinmetz, N., Coleman, T., Naidoo, N., Frank, M.G., Mechanisms of sleep-dependent consolidation of cortical plasticity. Neuron 61 (2009), 454–466.
25. 25 Dudai, Y., The restless engram: consolidations never end. Annu Rev Neurosci 35 (2012), 227–247.
26. 26 Dumoulin, M.C., Aton, S.J., Watson, A.J., Renouard, L., Coleman, T., Frank, M.G., Extracellular signal-regulated kinase (ERK) activity during sleep consolidates cortical plasticity in vivo. Cereb Cortex 25 (2015), 507–515.
27. 27 Seibt, J., Dumoulin, M., Aton, S.J., Naidoo, J., Watson, A., Coleman, T., Frank, M.G., Protein synthesis during sleep consolidates cortical plasticity in vivo. Curr Biol 22 (2012), 676–682.
28. 28 Rosenberg, T., Gal-Ben-Ari, S., Dieterich, D.C., Kreutz, M.R., Ziv, N.E., Gundelfinger, E.D., Rosenblum, K., The roles of protein expression in synaptic plasticity and memory consolidation. Front Mol Neurosci, 7, 2014.
29. 29 Aton, S.J., Broussard, C., Dumoulin, M., Seibt, J., Watson, A., Coleman, T., Frank, M.G., Visual experience and subsequent sleep induce sequential plastic changes in putative inhibitory and excitatory cortical neurons. PNAS 110 (2013), 3101–3106.
30. 30 Hennevin, E., Huetz, C., Edeline, J.-M., Neural representations during sleep: from sensory processing to memory traces. Neurobiol Learn Memory 87 (2007), 416–440.
31. 31 Wilson, M.A., McNaughton, B.L., Reactivation of hippocampal ensemble memories during sleep. Science 265 (1994), 676–682.
32. 32 Turrigiano, G., Too many cooks? Intrinsic and synaptic homeostatic mechanisms in cortical circuit refinement. Annu Rev Neurosci 34 (2011), 89–103.
33. 33 Turrigiano, G.G., The self-tuning neuron: synaptic scaling of excitatory synapses. Cell 135 (2008), 422–435.
34. 34 Burrone, J., Murthy, V.N., Synaptic gain control and homeostasis. Curr Opin Neurobiol 13 (2003), 560–567.
35. 35 Pozo, K., Goda, Y., Unraveling mechanisms of homeostatic synaptic plasticity. Neuron 66 (2010), 337–351.
36. 36•• Hengen, K.B., Torrado Pacheco, A., McGregor, J.N., Van Hooser, S.D., Turrigiano, G.G., Neuronal firing rate homeostasis is inhibited by sleep and promoted by wake. Cell 165 (2016), 180–191 This study showed that synaptic upscaling occurs during active waking and not sleep.
37. 37 Hengen, K.B., Lambo, M.E., Van Hooser, S.D., Katz, D.B., Turrigiano, G.G., Firing rate homeostasis in visual cortex of freely behaving rodents. Neuron 80 (2013), 335–342.
38. 38 Frank, M.G., Erasing synapses in sleep: is it time to be SHY?. Neural Plast, 2012, 2012.
39. 39 Jones, B.E., Basic mechanisms of sleep-waking states. Kryger, M.H., Roth, T., Dement, W.C., (eds.) Principles and Practice of Sleep Medicine, fourth edn, 2005, Saunders, 136–153.
40. 40• Tononi, G., Cirelli, C., Sleep and the price of plasticity: from synaptic and cellular homeostasis to memory consolidation and integration. Neuron 81 (2014), 12–34 A review of the synaptic homeostasis hypothesis, according to which sleep globally weakens synaptic strength.
41. 41• Frank, M.G., Cantera, R., Sleep, clocks, and synaptic plasticity. Trends Neurosci 37 (2014), 491–501 A counterpoint to Tononi and Cirelli, 2014. This review present evidence that sleep or circadian rhythms can strengthen synapses, depending on the circuit under examination.
42. 42 Fernandes, D., Carvalho, A.L., Mechanisms of homeostatic plasticity in the excitatory synapse. J Neurochem 139:6 (2016), 973–996.
43. 43 Cooke, S.F., Bear, M.F., How the mechanisms of long-term synaptic potentiation and depression serve experience-dependent plasticity in primary visual cortex. Philos Trans R Soc B Biol Sci, 369, 2014, 20130284.