Call it Worm Sleep

Trends in Neurosciences

Volumn 39, Issue 2, 2016, Pages 54-62

  Trojanowski, Nicholas F ^a   Raizen, David M ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Caenorhabditis elegans; Cellular stress; Development; Evolution; Quiescence; Sleep

Indexed keywords

CYCLIC AMP; CYCLIC GMP DEPENDENT PROTEIN KINASE; DOPAMINE; NEUROPEPTIDE; NEUROPEPTIDE PDF; UNCLASSIFIED DRUG; VASCULOTROPIN RECEPTOR; CAENORHABDITIS ELEGANS PROTEIN;

CAENORHABDITIS ELEGANS; CELLULAR STRESS RESPONSE; CIRCADIAN RHYTHM; HOMEOSTASIS; INSECT; MAMMAL; NEUROANATOMY; NONHUMAN; PRIORITY JOURNAL; REVIEW; SLEEP; ANIMAL; HUMAN; LOCOMOTION; NERVE CELL NETWORK; PHYSIOLOGY; SPECIES DIFFERENCE;

ANIMALS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; HUMANS; LOCOMOTION; NERVE NET; SLEEP; SPECIES SPECIFICITY;

EID: 84958851031     PISSN: 01662236     EISSN: 1878108X     Source Type: Journal    
DOI: 10.1016/j.tins.2015.12.005     Document Type: Review

References (101)

1. Benington J.H., Heller H.C. Restoration of brain energy metabolism as the function of sleep. Prog. Neurobiol. 1995, 45:347-360.
2. Mignot E. Why we sleep: the temporal organization of recovery. PLoS Biol. 2008, 6:e106.
3. Rechtschaffen A. Current perspectives on the function of sleep. Perspect. Biol. Med. 1998, 41:359-390.
4. Mackiewicz M., et al. Macromolecule biosynthesis: a key function of sleep. Physiol. Genomics 2007, 31:441-457.
5. Tononi G., Cirelli C. Sleep and the price of plasticity: from synaptic and cellular homeostasis to memory consolidation and integration. Neuron 2014, 81:12-34.
6. Frank M.G., Cantera R. Sleep, clocks, and synaptic plasticity. Trends Neurosci. 2014, 37:491-501.
7. Schmidt M.H. The energy allocation function of sleep: a unifying theory of sleep, torpor, and continuous wakefulness. Neurosci. Biobehav. Rev. 2014, 47:122-153.
8. Kleitman N. Sleep. Physiol. Rev. 1929, 9:624-665.
9. Loomis A.L., et al. Further observations on the potential rhythms of the cerebral cortex during sleep. Science 1935, 82:198-200.
10. Loomis A.L., et al. Cerebral states during sleep, as studied by human brain potentials. J. Exp. Psychol. 1937, 21:127-144.
11. Aserinsky E., Kleitman N. Regularly occurring periods of eye motility, and concomitant phenomena, during sleep. Science 1953, 118:273-274.
12. Dement W.C. The occurrence of low voltage, fast, electroencephalogram patterns during behavioral sleep in the cat. Electroencephalogr. Clin. Neurophysiol. 1958, 10:291-296.
13. Finelli L.A., et al. Dual electroencephalogram markers of human sleep homeostasis: correlation between theta activity in waking and slow-wave activity in sleep. Neuroscience 2000, 101:523-529.
14. Suzuki A., et al. Behavioral and biochemical dissociation of arousal and homeostatic sleep need influenced by prior wakeful experience in mice. Proc. Natl. Acad. Sci. U.S.A. 2013, 110:10288-10293.
15. Roffwarg H.P., et al. Ontogenetic development of the human sleep-dream cycle. Science 1966, 152:604-619.
16. Borbély A.A. A two process model of sleep regulation. Hum. Neurobiol. 1982, 1:195-204.
17. Krueger J.M., et al. Sleep-promoting effects of muramyl peptides. Proc. Natl. Acad. Sci. U.S.A. 1982, 79:6102-6106.
18. Toth L.A., Krueger J.M. Alteration of sleep in rabbits by Staphylococcus aureus infection. Infect. Immun. 1988, 56:1785-1791.
19. Saper C.B., et al. Hypothalamic regulation of sleep and circadian rhythms. Nature 2005, 437:1257-1263.
20. Imeri L., Opp M.R. How (and why) the immune system makes us sleep. Nat. Rev. Neurosci. 2009, 10:199-210.
21. Siegel J.M. Clues to the functions of mammalian sleep. Nature 2005, 437:1264-1271.
22. Blumberg M.S., et al. The development of sleep-wake rhythms and the search for elemental circuits in the infant brain. Behav. Neurosci. 2014, 128:250-263.
23. Zhdanova I.V., et al. Melatonin promotes sleep-like state in zebrafish. Brain Res. 2001, 903:263-268.
24. Hendricks J.C., et al. Rest in Drosophila is a sleep-like state. Neuron 2000, 25:129-138.
25. Shaw P.J., et al. Correlates of sleep and waking in Drosophila melanogaster. Science 2000, 287:1834-1837.
26. Campbell S.S., Tobler I. Animal sleep: a review of sleep duration across phylogeny. Neurosci. Biobehav. Rev. 1984, 8:269-300.
27. Hendricks J.C., et al. The need for a simple animal model to understand sleep. Prog. Neurobiol. 2000, 61:339-351.
28. Zimmerman J.E., et al. Conservation of sleep: insights from non-mammalian model systems. Trends Neurosci. 2008, 31:371-376.
29. Raizen D.M., et al. Lethargus is a Caenorhabditis elegans sleep-like state. Nature 2008, 451:569-572.
30. Hill A.J., et al. Cellular stress induces a protective sleep-like state in C. elegans. Curr. Biol. 2014, 24:2399-2405.
31. Cassada R.C., Russell R.L. The dauerlarva, a post-embryonic developmental variant of the nematode Caenorhabditis elegans. Dev. Biol. 1975, 46:326-342.
32. Iwanir S., et al. The microarchitecture of C. elegans behavior during lethargus: homeostatic bout dynamics, a typical body posture, and regulation by a central neuron. Sleep 2013, 36:385-395.
33. Tramm N., et al. Why do sleeping nematodes adopt a hockey-stick-like posture?. PLoS ONE 2014, 9:e101162.
34. Schwarz J., et al. Reduced muscle contraction and a relaxed posture during sleep-like lethargus. Worm 2012, 1:11-13.
35. Cho J.Y., Sternberg P.W. Multilevel modulation of a sensory motor circuit during C. elegans sleep and arousal. Cell 2014, 156:249-260.
36. Schwarz J., et al. Reduced activity of a sensory neuron during a sleep-like state in Caenorhabditis elegans. Curr. Biol. 2011, 21:R983-R984.
37. Driver R.J., et al. DAF-16/FOXO regulates homeostasis of essential sleep-like behavior during larval transitions in C. elegans. Curr. Biol. 2013, 23:501-506.
38. Jones D., Candido E.P. Feeding is inhibited by sublethal concentrations of toxicants and by heat stress in the nematode Caenorhabditis elegans: relationship to the cellular stress response. J. Exp. Zoolog. 1999, 284:147-157.
39. You Y-J., et al. Insulin, cGMP, and TGF-β signals regulate food intake and quiescence in C. elegans: a model for satiety. Cell Metab. 2008, 7:249-257.
40. Gallagher T., et al. ASI regulates satiety quiescence in C. elegans. J. Neurosci. 2013, 33:9716-9724.
41. Pittendrigh C.S. On temperature independence in the clock system controlling emergence time in Drosophila. Proc. Natl. Acad. Sci. U.S.A. 1954, 40:1018-1029.
42. Pittendrigh C.S. Circadian rhythms and the circadian organization of living systems. Cold Spring Harb. Symp. Quant. Biol. 1960, 25:159-184.
43. Stanewsky R. Genetic analysis of the circadian system in Drosophila melanogaster and mammals. J. Neurobiol. 2002, 54:111-147.
44. Cirelli C., et al. Reduced sleep in Drosophila Shaker mutants. Nature 2005, 434:1087-1092.
45. Konopka R.J., Benzer S. Clock mutants of Drosophila melanogaster. Proc. Natl. Acad. Sci. U.S.A. 1971, 68:2112-2116.
46. Hardin P.E., et al. Feedback of the Drosophila period gene product on circadian cycling of its messenger RNA levels. Nature 1990, 343:536-540.
47. Sun Z.S., et al. RIGUI, a putative mammalian ortholog of the Drosophila period gene. Cell 1997, 90:1003-1011.
48. Tei H., et al. Circadian oscillation of a mammalian homologue of the Drosophila period gene. Nature 1997, 389:512-516.
49. van der Linden A.M., et al. Genome-wide analysis of light- and temperature-entrained circadian transcripts in Caenorhabditis elegans. PLoS Biol. 2010, 8:e1000503.
50. Jeon M., et al. Similarity of the C. elegans developmental timing protein LIN-42 to circadian rhythm proteins. Science 1999, 286:1141-1146.
51. Frand A.R., et al. Functional genomic analysis of C. elegans molting. PLoS Biol. 2005, 3:e312.
52. Monsalve G.C., et al. LIN-42/PERIOD controls cyclical and developmental progression of C. elegans molts. Curr. Biol. 2011, 21:2033-2045.
53. Singh K., et al. Deep conservation of genes required for both Drosophila melanogaster and Caenorhabditis elegans sleep includes a role for dopaminergic signaling. Sleep 2014, 37:1439-1451.
54. Choi S., et al. Sensory neurons arouse C. elegans locomotion via both glutamate and neuropeptide release. PLoS Genet 2015, 11:e1005359.
55. Tomita J., et al. The NMDA receptor promotes sleep in the fruit fly, Drosophila melanogaster. PLoS ONE 2015, 10:e0128101.
56. Renn S.C., et al. A pdf neuropeptide gene mutation and ablation of PDF neurons each cause severe abnormalities of behavioral circadian rhythms in Drosophila. Cell 1999, 99:791-802.
57. Taghert P.H., Nitabach M.N. Peptide neuromodulation in invertebrate model systems. Neuron 2012, 76:82-97.
58. Parisky K.M., et al. PDF cells are a GABA-responsive wake-promoting component of the Drosophila sleep circuit. Neuron 2008, 60:672-682.
59. Choi S., et al. Analysis of NPR-1 reveals a circuit mechanism for behavioral quiescence in C. elegans. Neuron 2013, 78:869-880.
60. Sheeba V., et al. Large ventral lateral neurons modulate arousal and sleep in Drosophila. Curr. Biol. 2008, 18:1537-1545.
61. Kushikata T., et al. Epidermal growth factor enhances spontaneous sleep in rabbits. Am. J. Physiol. 1998, 275:R509-R514.
62. Kramer A., et al. Regulation of daily locomotor activity and sleep by hypothalamic EGF receptor signaling. Science 2001, 294:2511-2515.
63. Foltenyi K., et al. Activation of EGFR and ERK by rhomboid signaling regulates the consolidation and maintenance of sleep in Drosophila. Nat. Neurosci. 2007, 10:1160-1167.
64. Van Buskirk C., Sternberg P.W. Epidermal growth factor signaling induces behavioral quiescence in Caenorhabditis elegans. Nat. Neurosci. 2007, 10:1300-1307.
65. Ginty D.D., et al. Regulation of CREB phosphorylation in the suprachiasmatic nucleus by light and a circadian clock. Science 1993, 260:238-241.
66. Graves L.A., et al. Genetic evidence for a role of CREB in sustained cortical arousal. J. Neurophysiol. 2003, 90:1152-1159.
67. Hendricks J.C., et al. A non-circadian role for cAMP signaling and CREB activity in Drosophila rest homeostasis. Nat. Neurosci. 2001, 4:1108-1115.
68. Belfer S.J., et al. Caenorhabditis-in-drop array for monitoring C. elegans quiescent behavior. Sleep 2013, 36:689-698G.
69. Trulson M.E. Simultaneous recording of substantia nigra neurons and voltammetric release of dopamine in the caudate of behaving cats. Brain Res. Bull. 1985, 15:221-223.
70. Wisor J.P., et al. Dopaminergic role in stimulant-induced wakefulness. J. Neurosci. 2001, 21:1787-1794.
71. Andretic R., et al. Dopaminergic modulation of arousal in Drosophila. Curr. Biol. 2005, 15:1165-1175.
72. Kume K., et al. Dopamine is a regulator of arousal in the fruit fly. J. Neurosci. 2005, 25:7377-7384.
73. Liu Q., et al. Two dopaminergic neurons signal to the dorsal fan-shaped body to promote wakefulness in Drosophila. Curr. Biol. 2012, 22:2114-2123.
74. Ueno T., et al. Identification of a dopamine pathway that regulates sleep and arousal in Drosophila. Nat. Neurosci. 2012, 15:1516-1523.
75. Donlea J.M., et al. Foraging alters resilience/vulnerability to sleep disruption and starvation in Drosophila. Proc. Natl. Acad. Sci. U.S.A. 2012, 109:2613-2618.
76. Langmesser S., et al. cGMP-dependent protein kinase type I is implicated in the regulation of the timing and quality of sleep and wakefulness. PLoS ONE 2009, 4:e4238.
77. Rampin C., et al. Immobilisation stress induces a paradoxical sleep rebound in rat. Neurosci. Lett. 1991, 126:113-118.
78. Dabbish N.S., Raizen D.M. GABAergic synaptic plasticity during a developmentally regulated sleep-like state in C. elegans. J. Neurosci. 2011, 31:15932-15943.
79. Singh R.N., Sulston J.E. Some observations on moulting in Caenorhabditis elegans. Nematologica 1978, 24:63-71.
80. George-Raizen J.B., et al. Dynamically-expressed prion-like proteins form a cuticle in the pharynx of Caenorhabditis elegans. Biol. Open 2014, 3:1139-1149.
81. Hedgecock E.M., White J.G. Polyploid tissues in the nematode Caenorhabditis elegans. Dev. Biol. 1985, 107:128-133.
82. Williams J.A., et al. Interaction between sleep and the immune response in Drosophila: a role for the NFkappaB relish. Sleep 2007, 30:389-400.
83. Livingstone M.S., Hubel D.H. Effects of sleep and arousal on the processing of visual information in the cat. Nature 1981, 291:554-561.
84. Kayser M.S., et al. A critical period of sleep for development of courtship circuitry and behavior in Drosophila. Science 2014, 344:269-274.
85. Turek M., et al. An AP2 transcription factor is required for a sleep-active neuron to induce sleep-like quiescence in C. elegans. Curr. Biol. 2013, 23:2215-2223.
86. Nelson M.D., et al. The neuropeptide NLP-22 regulates a sleep-like state in Caenorhabditis elegans. Nat. Commun. 2013, 4:2846.
87. Nelson M.D., et al. FMRFamide-like FLP-13 neuropeptides promote quiescence following heat stress in Caenorhabditis elegans. Curr. Biol. 2014, 24:2406-2410.
88. Janssen T., et al. Discovery and characterization of a conserved pigment dispersing factor-like neuropeptide pathway in Caenorhabditis elegans. J. Neurochem. 2009, 111:228-241.
89. Trojanowski N.F., et al. Distinct mechanisms underlie quiescence during two Caenorhabditis elegans sleep-like states. J. Neurosci. 2015, 35:14571-14584.
90. van Alphen B., et al. A dynamic deep sleep stage in Drosophila. J. Neurosci. 2013, 33:6917-6927.
91. Metaxakis A., et al. Lowered insulin signalling ameliorates age-related sleep fragmentation in Drosophila. PLoS Biol. 2014, 12:e1001824.
92. Lenz O., et al. Brain, behavior, and immunity. Brain Behav. Immun. 2015, 47:141-148.
93. Nagy S., et al. Homeostasis in C. elegans sleep is characterized by two behaviorally and genetically distinct mechanisms. Elife 2014, 3:e04380.
94. Seidner G., et al. Identification of neurons with a privileged role in sleep homeostasis in Drosophila melanogaster. Curr. Biol. 2015, 25:2928-2938.
95. He C., et al. Regulation of sleep by neuropeptide Y-like system in Drosophila melanogaster. PLoS ONE 2013, 8:e74237.
96. Antonijevic I.A., et al. Neuropeptide Y promotes sleep and inhibits ACTH and cortisol release in young men. Neuropharmacology 2000, 39:1474-1481.
97. Kato S., et al. Global brain dynamics embed the motor command sequence of Caenorhabditis elegans. Cell 2015, 163:656-669.
98. Trojanowski N.F., et al. Neural and genetic degeneracy underlies Caenorhabditis elegans feeding behavior. J. Neurophysiol. 2014, 112:951-961.
99. Stirman J.N., et al. Real-time multimodal optical control of neurons and muscles in freely behaving Caenorhabditis elegans. Nat. Methods 2011, 8:153-158.
100. Leifer A.M., et al. Optogenetic manipulation of neural activity in freely moving Caenorhabditis elegans. Nat. Methods 2011, 8:147-152.
101. Kocabas A., et al. Controlling interneuron activity in Caenorhabditis elegans to evoke chemotactic behaviour. Nature 2012, 490:273-277.