www.sciencemag.org/content/344/6188/1173/suppl/DC1 Supplementary Materials for Sleep promotes branch-specific formation of dendritic spines after learning Guang Yang, Cora Sau Wan Lai, Joseph Cichon, Lei Ma, Wei Li, Wen-Biao Gan* *Corresponding author. E-mail: [email protected]Published 6 June 2014, Science 344, 1173 (2014) DOI: 10.1126/science.1249098 This PDF file includes Materials and Methods Figs. S1 to S8 References
19
Embed
Supplementary Materials for - Science...Supplementary Materials for Sleep promotes branch-specific formation of dendritic spines after learning Guang Yang, Cora Sau Wan Lai, Joseph
This document is posted to help you gain knowledge. Please leave a comment to let me know what you think about it! Share it to your friends and learn new things together.
4. S. Diekelmann, J. Born, The memory function of sleep. Nat. Rev. Neurosci. 11, 114–126 (2010). Medline
5. J. H. Benington, M. G. Frank, Cellular and molecular connections between sleep and synaptic plasticity. Prog. Neurobiol. 69, 71–101 (2003). Medline doi:10.1016/S0301-0082(03)00018-2
6. C. Pavlides, J. Winson, Influences of hippocampal place cell firing in the awake state on the activity of these cells during subsequent sleep episodes. J. Neurosci. 9, 2907–2918 (1989). Medline
7. W. E. Skaggs, B. L. McNaughton, Replay of neuronal firing sequences in rat hippocampus during sleep following spatial experience. Science 271, 1870–1873 (1996). Medline doi:10.1126/science.271.5257.1870
8. A. S. Dave, D. Margoliash, Song replay during sleep and computational rules for sensorimotor vocal learning. Science 290, 812–816 (2000). Medline doi:10.1126/science.290.5492.812
9. M. A. Wilson, B. L. McNaughton, Reactivation of hippocampal ensemble memories during sleep. Science 265, 676–679 (1994). Medline doi:10.1126/science.8036517
10. D. Ji, M. A. Wilson, Coordinated memory replay in the visual cortex and hippocampus during sleep. Nat. Neurosci. 10, 100–107 (2007). Medline doi:10.1038/nn1825
11. S. Ribeiro, D. Gervasoni, E. S. Soares, Y. Zhou, S. C. Lin, J. Pantoja, M. Lavine, M. A. Nicolelis, Long-lasting novelty-induced neuronal reverberation during slow-wave sleep in multiple forebrain areas. PLoS Biol. 2, E24 (2004). Medline doi:10.1371/journal.pbio.0020024
12. A. S. Dave, A. C. Yu, D. Margoliash, Behavioral state modulation of auditory activity in a vocal motor system. Science 282, 2250–2254 (1998). Medline doi:10.1126/science.282.5397.2250
13. R. R. Llinás, M. Steriade, Bursting of thalamic neurons and states of vigilance. J. Neurophysiol. 95, 3297–3308 (2006). Medline doi:10.1152/jn.00166.2006
14. V. Crunelli, S. W. Hughes, The slow (<1 Hz) rhythm of non-REM sleep: A dialogue between three cardinal oscillators. Nat. Neurosci. 13, 9–17 (2010). Medline doi:10.1038/nn.2445
15. C. H. Bailey, E. R. Kandel, Structural changes accompanying memory storage. Annu. Rev. Physiol. 55, 397–426 (1993). Medline doi:10.1146/annurev.ph.55.030193.002145
16. J. W. Lichtman, H. Colman, Synapse elimination and indelible memory. Neuron 25, 269–278 (2000). Medline doi:10.1016/S0896-6273(00)80893-4
17. D. H. Bhatt, S. Zhang, W. B. Gan, Dendritic spine dynamics. Annu. Rev. Physiol. 71, 261–282 (2009). Medline doi:10.1146/annurev.physiol.010908.163140
18. G. Yang, F. Pan, W. B. Gan, Stably maintained dendritic spines are associated with lifelong memories. Nature 462, 920–924 (2009). Medline doi:10.1038/nature08577
19. I. Timofeev, Neuronal plasticity and thalamocortical sleep and waking oscillations. Prog. Brain Res. 193, 121–144 (2011). Medline doi:10.1016/B978-0-444-53839-0.00009-0
20. G. Wang, B. Grone, D. Colas, L. Appelbaum, P. Mourrain, Synaptic plasticity in sleep: learning, homeostasis and disease. Trends Neurosci. 34, 452–463 (2011). Medline doi:10.1016/j.tins.2011.07.005
21. M. G. Frank, Erasing synapses in sleep: Is it time to be SHY? Neural Plast. 2012, 264378 (2012). Medline doi:10.1155/2012/264378
22. J. Born, G. B. Feld, Sleep to upscale, sleep to downscale: Balancing homeostasis and plasticity. Neuron 75, 933–935 (2012). Medline doi:10.1016/j.neuron.2012.09.007
23. C. Cirelli, G. Tononi, Differences in gene expression during sleep and wakefulness. Ann. Med. 31, 117–124 (1999). Medline doi:10.3109/07853899908998787
24. V. V. Vyazovskiy, C. Cirelli, M. Pfister-Genskow, U. Faraguna, G. Tononi, Molecular and electrophysiological evidence for net synaptic potentiation in wake and depression in sleep. Nat. Neurosci. 11, 200–208 (2008). Medline doi:10.1038/nn2035
25. S. Maret, U. Faraguna, A. B. Nelson, C. Cirelli, G. Tononi, Sleep and waking modulate spine turnover in the adolescent mouse cortex. Nat. Neurosci. 14, 1418–1420 (2011). Medline doi:10.1038/nn.2934
26. G. Yang, W. B. Gan, Sleep contributes to dendritic spine formation and elimination in the developing mouse somatosensory cortex. Dev. Neurobiol. 72, 1391–1398 (2012). Medline doi:10.1002/dneu.20996
27. J. M. Donlea, N. Ramanan, P. J. Shaw, Use-dependent plasticity in clock neurons regulates sleep need in Drosophila. Science 324, 105–108 (2009). Medline doi:10.1126/science.1166657
28. D. Bushey, G. Tononi, C. Cirelli, Sleep and synaptic homeostasis: Structural evidence in Drosophila. Science 332, 1576–1581 (2011). Medline doi:10.1126/science.1202839
29. G. Tononi, C. Cirelli, Sleep and synaptic homeostasis: A hypothesis. Brain Res. Bull. 62, 143–150 (2003). Medline doi:10.1016/j.brainresbull.2003.09.004
30. M. G. Frank, N. P. Issa, M. P. Stryker, Sleep enhances plasticity in the developing visual cortex. Neuron 30, 275–287 (2001). Medline doi:10.1016/S0896-6273(01)00279-3
31. S. Chauvette, J. Seigneur, I. Timofeev, Sleep oscillations in the thalamocortical system induce long-term neuronal plasticity. Neuron 75, 1105–1113 (2012). Medline doi:10.1016/j.neuron.2012.08.034
32. S. J. Aton, J. Seibt, M. Dumoulin, S. K. Jha, N. Steinmetz, T. Coleman, N. Naidoo, M. G. Frank, Mechanisms of sleep-dependent consolidation of cortical plasticity. Neuron 61, 454–466 (2009). Medline doi:10.1016/j.neuron.2009.01.007
33. J. Seibt, M. C. Dumoulin, S. J. Aton, T. Coleman, A. Watson, N. Naidoo, M. G. Frank, Protein synthesis during sleep consolidates cortical plasticity in vivo. Curr. Biol. 22, 676–682 (2012). Medline doi:10.1016/j.cub.2012.02.016
34. H. P. Roffwarg, J. N. Muzio, W. C. Dement, Ontogenetic development of the human sleep-dream cycle. Science 152, 604–619 (1966). Medline doi:10.1126/science.152.3722.604
35. D. Jouvet-Mounier, L. Astic, D. Lacote, Ontogenesis of the states of sleep in rat, cat, and guinea pig during the first postnatal month. Dev. Psychobiol. 2, 216–239 (1969). Medline doi:10.1002/dev.420020407
36. C. Liston, J. M. Cichon, F. Jeanneteau, Z. Jia, M. V. Chao, W. B. Gan, Circadian glucocorticoid oscillations promote learning-dependent synapse formation and maintenance. Nat. Neurosci. 16, 698–705 (2013). Medline doi:10.1038/nn.3387
37. G. Yang, F. Pan, P. C. Chang, F. Gooden, W. B. Gan, Transcranial two-photon imaging of synaptic structures in the cortex of awake head-restrained mice. Methods Mol. Biol. 1010, 35–43 (2013). Medline doi:10.1007/978-1-62703-411-1_3
38. P. V. Zelenin, T. G. Deliagina, G. N. Orlovsky, A. Karayannidou, E. E. Stout, M. G. Sirota, I. N. Beloozerova, Activity of motor cortex neurons during backward locomotion. J. Neurophysiol. 105, 2698–2714 (2011). Medline doi:10.1152/jn.00120.2011
39. T. W. Chen, T. J. Wardill, Y. Sun, S. R. Pulver, S. L. Renninger, A. Baohan, E. R. Schreiter, R. A. Kerr, M. B. Orger, V. Jayaraman, L. L. Looger, K. Svoboda, D. S. Kim, Ultrasensitive fluorescent proteins for imaging neuronal activity. Nature 499, 295–300 (2013). Medline doi:10.1038/nature12354
40. I. G. Campbell, I. Feinberg, NREM delta stimulation following MK-801 is a response of sleep systems. J. Neurophysiol. 76, 3714–3720 (1996). Medline
41. C. X. Li, R. S. Waters, Organization of the mouse motor cortex studied by retrograde tracing and intracortical microstimulation (ICMS) mapping. Can. J. Neurol. Sci. 18, 28–38 (1991). Medline
42. G. Yang, F. Pan, C. N. Parkhurst, J. Grutzendler, W. B. Gan, Thinned-skull cranial window technique for long-term imaging of the cortex in live mice. Nat. Protoc. 5, 201–208 (2010). Medline doi:10.1038/nprot.2009.222
43. K. A. Tennant, D. L. Adkins, N. A. Donlan, A. L. Asay, N. Thomas, J. A. Kleim, T. A. Jones, The organization of the forelimb representation of the C57BL/6 mouse motor cortex as defined by intracortical microstimulation and cytoarchitecture. Cereb. Cortex 21, 865–876 (2011). Medline doi:10.1093/cercor/bhq159