Life without Food and the Implications for Neurodegeneration

Advances in Genetics

Volumn 92, Issue , 2015, Pages 53-74

  Calixto, Andrea ^a  

^a UNIVERSIDAD MAYOR   (Chile)

Author keywords

Dauer; Diapause; Dlk 1; Mec 4d; Neurodegeneration; Regeneration

Indexed keywords

ANIMAL; CAENORHABDITIS ELEGANS; CYTOLOGY; DIAPAUSE; GROWTH, DEVELOPMENT AND AGING; HIBERNATION; MAMMAL; NERVE CELL; NEUROPROTECTION; PHYSIOLOGY; STARVATION;

ANIMALS; CAENORHABDITIS ELEGANS; DIAPAUSE, INSECT; HIBERNATION; MAMMALS; NEURONS; NEUROPROTECTION; STARVATION;

EID: 84973407198     PISSN: 00652660     EISSN: None     Source Type: Book Series    
DOI: 10.1016/bs.adgen.2015.09.004     Document Type: Article

References (96)

1. Alonso Mejia A., Rendon-Salinas E., Montecinos-Patiño E., Brower L.P. Use of lipid reserves by monarch butterflies overwintering in Mexico: implications for conservation. Ecological Applications 1997, 7:934-947.
2. Antebi A., Yeh W.H., Tait D., Hedgecock E.M., Riddle D.L. daf-12 encodes a nuclear receptor that regulates the dauer diapause and developmental age in C. elegans. Genes and Development 2000, 14:1512-1527.
3. Ascher P., Nowak L. A patch-clamp study of excitatory amino acid activated channels. Advances in Experimental Medicine and Biology 1986, 203:507-511.
4. Barnes B.M. Freeze avoidance in a mammal: body temperatures below 0 degree C in an Arctic hibernator. Science 1989, 244:1593-1595.
5. Bianchi L., Gerstbrein B., Frøkjaer-Jensen C., Royal D.C., Mukherjee G., Royal M.A., et al. The neurotoxic MEC-4(d) DEG/ENaC sodium channel conducts calcium: implications for necrosis initiation. Nature Neuroscience 2004, 7:1337-1344.
6. Birnby D.A., Link E.M., Vowels J.J., Tian H., Colacurcio P.L., Thomas J.H. A transmembrane guanylyl cyclase (DAF-11) and Hsp90 (DAF-21) regulate a common set of chemosensory behaviors in Caenorhabditis elegans. Genetics 2000, 155:85-104.
7. Braeckman B.P., Houthoofd K., Vanfleteren J.R. Patterns of metabolic activity during aging of the wild type and longevity mutants of Caenorhabditis elegans. Journal of the American Aging Association 2000, 23:55-73.
8. Braeckman B.P., Houthoofd K., Vanfleteren J.R. Intermediary metabolism. WormBook 2009, 1-24.
9. Budd S.L. Mechanisms of neuronal damage in brain hypoxia/ischemia: focus on the role of mitochondrial calcium accumulation. Pharmacology and Therapeutics 1998, 80:203-229.
10. Burnell A.M., Houthoofd K., O'Hanlon K., Vanfleteren J.R. Alternate metabolism during the dauer stage of the nematode Caenorhabditis elegans. Experimental Gerontology 2005, 40:850-856.
11. Butcher R.A., Fujita M., Schroeder F.C., Clardy J. Small-molecule pheromones that control dauer development in Caenorhabditis elegans. Nature Chemical Biology 2007, 3:420-422.
12. Butcher R.A., Ragains J.R., Kim E., Clardy J. A potent dauer pheromone component in Caenorhabditis elegans that acts synergistically with other components. Proceedings of the National Academy of Sciences of the United States of America 2008, 105:14288-14292.
13. Byrne A.B., Walradt T., Gardner K.E., Hubbert A., Reinke V., Hammarlund M. Insulin/IGF1 signaling inhibits age-dependent axon regeneration. Neuron 2014, 81:561-573.
14. Calixto A., Jara J.S., Court F.A. Diapause formation and downregulation of insulin-like signaling via DAF-16/FOXO delays axonal degeneration and neuronal loss. PLOS Genetics 2012, 8:e1003141.
15. Cassada R.C., Russell R.L. The dauer larva, a post-embryonic developmental variant of the nematode Caenorhabditis elegans. Developmental Biology 1975, 46:326-342.
16. Chalfie M., Wolinsky E. The identification and suppression of inherited neurodegeneration in Caenorhabditis elegans. Nature 1990, 345:410-416.
17. Chen L., Wang Z., Ghosh-Roy A., Hubert T., Yan D., O'Rourke S., et al. Axon regeneration pathways identified by systematic genetic screening in C. elegans. Neuron 2011, 71:1043-1057.
18. Choi D.W. Calcium: still center-stage in hypoxic-ischemic neuronal death. Trends in Neurosciences 1995, 18:58-60.
19. Chung S., Gumienny T.L., Hengartner M.O., Driscoll M. A common set of engulfment genes mediates removal of both apoptotic and necrotic cell corpses in C. elegans. Nature Cell Biology 2000, 2:931-937.
20. Chung S.H., Schmalz A., Ruiz R.C., Gabel C.V., Mazur E. Femtosecond laser ablation reveals antagonistic sensory and neuroendocrine signaling that underlie C. elegans behavior and development. Cell Reports 2013, 4:316-326.
21. Clarke R.J., Catauro M., Rasmussen H.H., Apell H.J. Quantitative calculation of the role of the Na(+),K(+)-ATPase in thermogenesis. Biochimica et Biophysica Acta 2013, 1827:1205-1212.
22. Cook A., Franks C.J., Holden-Dye L. Electrophysiological recordings from the pharynx. WormBook 2006, 1-7.
23. Croll N.A., Matthews B.E. Biology of nematodes 1977, Blackie, Glasgow.
24. Dave K.R., Christian S.L., Perez-Pinzon M.A., Drew K.L. Neuroprotection: lessons from hibernators. Comparative Biochemistry and Physiology Part B: Biochemistry Molecular Biology 2012, 162:1-9.
25. Drew K.L., Osborne P.G., Frerichs K.U., Hu Y., Koren R.E., Hallenbeck J.M., et al. Ascorbate and glutathione regulation in hibernating ground squirrels. Brain Research 1999, 851:1-8.
26. Edison A.S. Caenorhabditis elegans pheromones regulate multiple complex behaviors. Current Opinion in Neurobiology 2009, 19:378-388.
27. Fielenbach N., Antebi A. C. elegans dauer formation and the molecular basis of plasticity. Genes and Development 2008, 22:2149-2165.
28. Franks C.J., Pemberton D., Vinogradova I., Cook A., Walker R.J., Holden-Dye L. Ionic basis of the resting membrane potential and action potential in the pharyngeal muscle of Caenorhabditis elegans. Journal of Neurophysiology 2002, 87:954-961.
29. Fuchs S., Bundy J.G., Davies S.K., Viney J.M., Swire J.S., Leroi A.M. A metabolic signature of long life in Caenorhabditis elegans. BMC Biology 2010, 8:14.
30. Gao S., Zhen M. Action potentials drive body wall muscle contractions in Caenorhabditis elegans. Proceedings of the National Academy of Sciences of the United States of America 2011, 108:2557-2562.
31. Gems D., Riddle D.L. Defining wild-type life span in Caenorhabditis elegans. The Journals of Gerontology Series A Biological Sciences and Medical Sciences 2000, 55:B215-B219.
32. Ghosh-Roy A., Wu Z., Goncharov A., Jin Y., Chisholm A.D. Calcium and cyclic AMP promote axonal regeneration in Caenorhabditis elegans and require DLK-1 kinase. Journal of Neuroscience 2010, 30:3175-3183.
33. Ghosh-Roy A., Goncharov A., Jin Y., Chisholm A.D. Kinesin-13 and tubulin posttranslational modifications regulate microtubule growth in axon regeneration. Developmental Cell 2012, 23:716-728.
34. Golden J.W., Riddle D.L. The Caenorhabditis elegans dauer larva: developmental effects of pheromone, food, and temperature. Developmental Biology 1984, 102:368-378.
35. Golden J.W., Riddle D.L. A Caenorhabditis elegans dauer-inducing pheromone and an antagonistic component of the food supply. Journal of Chemical Ecology 1984, 10:1265-1280.
36. Golden J.W., Riddle D.L. A pheromone-induced developmental switch in Caenorhabditis elegans: temperature-sensitive mutants reveal a wild-type temperature-dependent process. Proceedings of the National Academy of Sciences of the United States of America 1984, 81:819-823.
37. Gottlieb S., Ruvkun G. daf-2, daf-16 and daf-23: genetically interacting genes controlling Dauer formation in Caenorhabditis elegans. Genetics 1994, 137:107-120.
38. Hahn D.A., Denlinger D.L. Meeting the energetic demands of insect diapause: nutrient storage and utilization. Journal of Insect Physiology 2007, 53:760-773.
39. Hammarlund M., Jorgensen E.M., Bastiani M.J. Axons break in animals lacking beta-spectrin. Journal of Cell Biology 2007, 176:269-275.
40. Hammarlund M., Nix P., Hauth L., Jorgensen E.M., Bastiani M. Axon regeneration requires a conserved MAP kinase pathway. Science 2009, 323:802-806.
41. Hand S.C., Menze M.A., Borcar A., Patil Y., Covi J.A., Reynolds J.A., et al. Metabolic restructuring during energy-limited states: insights from Artemia franciscana embryos and other animals. Journal of Insect Physiology 2011, 57:584-594.
42. Hindle A.G., Martin S.L. Cytoskeletal regulation dominates temperature-sensitive proteomic changes of hibernation in forebrain of 13-lined ground squirrels. PLoS One 2013, 8:e71627.
43. Holt S.J., Riddle D.L. SAGE surveys C. elegans carbohydrate metabolism: evidence for an anaerobic shift in the long-lived dauer larva. Mechanisms of Ageing and Development 2003, 124:779-800.
44. Honda Y., Honda S. The daf-2 gene network for longevity regulates oxidative stress resistance and Mn-superoxide dismutase gene expression in Caenorhabditis elegans. FASEB Journal 1999, 13:1385-1393.
45. Houthoofd K., Braeckman B.P., Lenaerts I., Brys K., De Vreese A., Van Eygen S., et al. Ageing is reversed, and metabolism is reset to young levels in recovering dauer larvae of C. elegans. Experimental Gerontology 2002, 37:1015-1021.
46. Hu P.J. Dauer. WormBook 2007, 1-19.
47. Jeong P.Y., Jung M., Yim Y.H., Kim H., Park M., Hong E., et al. Chemical structure and biological activity of the Caenorhabditis elegans dauer-inducing pheromone. Nature 2005, 433:541-545.
48. Jones S.J., Riddle D.L., Pouzyrev A.T., Velculescu V.E., Hillier L., Eddy S.R., et al. Changes in gene expression associated with developmental arrest and longevity in Caenorhabditis elegans. Genome Research 2001, 11:1346-1352.
49. Kimura K.D., Tissenbaum H.A., Liu Y., Ruvkun G. daf-2, an insulin receptor-like gene that regulates longevity and diapause in Caenorhabditis elegans. Science 1997, 277:942-946.
50. Lant B., Storey K.B. An overview of stress response and hypometabolic strategies in Caenorhabditis elegans: conserved and contrasting signals with the mammalian system. International Journal of Biological Science 2010, 6:9-50.
51. Larsen P.L., Albert P.S., Riddle D.L. Genes that regulate both development and longevity in Caenorhabditis elegans. Genetics 1995, 139:1567-1583.
52. Liu F., Thatcher J.D., Epstein H.F. Induction of glyoxylate cycle expression in Caenorhabditis elegans: a fasting response throughout larval development. Biochemistry 1997, 36:255-260.
53. Ma Y.L., Zhu X., Rivera P.M., Tøien Ø., Barnes B.M., LaManna J.C., et al. Absence of cellular stress in brain after hypoxia induced by arousal from hibernation in Arctic ground squirrels. American Journal of Physiology. Regulatory, Integrative and Comparative Physiology 2005, 289:R1297-R1306.
54. McMullen D.C., Storey K.B. Suppression of Na+K+ -ATPase activity by reversible phosphorylation over the winter in a freeze-tolerant insect. Journal of Insect Physiology 2008, 54:1023-1027.
55. Narbonne P., Roy R. Caenorhabditis elegans dauers need LKB1/AMPK to ration lipid reserves and ensure long-term survival. Nature 2009, 457:210-214.
56. Nix P., Hammarlund M., Hauth L., Lachnit M., Jorgensen E.M., Bastiani M. Axon regeneration genes identified by RNAi screening in C. elegans. Journal of Neuroscience 2014, 34:629-645.
57. Nix P., Hisamoto N., Matsumoto K., Bastiani M. Axon regeneration requires coordinate activation of p38 and JNK MAPK pathways. Proceedings of the National Academy of Sciences of the United States of America 2011, 108:10738-10743.
58. Ogg S., Paradis S., Gottlieb S., Patterson G.I., Lee L., Tissenbaum H.A., et al. The Fork head transcription factor DAF-16 transduces insulin-like metabolic and longevity signals in C. elegans. Nature 1997, 389:994-999.
59. O'Hagan R., Chalfie M., Goodman M.B. The MEC-4 DEG/ENaC channel of Caenorhabditis elegans touch receptor neurons transduces mechanical signals. Nature Neuroscience 2005, 8:43-50.
60. O'riordan V.B., Burnell A.M. Intermediary metabolism in the dauer larvae of the nematode Caenorhabditis elegans. 1. Glycolysis, gluconeogenesis, oxidative phosphorylation and the tricarboxylic-acid cycle. Comparative Biochemistry and Physiology Part B: Biochemistry Molecular Biology 1989, 92:233-238.
61. O'riordan V.B., Burnell A.M. Intermediary metabolism in the dauer larvae of the nematode Caenorhabditis elegans. 2. The glyoxylate cycle and fatty-acid oxidation. Comparative Biochemistry and Physiology Part B: Biochemistry Molecular Biology 1990, 95:125-130.
62. Orr A.L., Lohse L.A., Drew K.L., Hermes-Lima M. Physiological oxidative stress after arousal from hibernation in Arctic ground squirrel. Comparative Biochemistry and Physiology Part A: Molecular Integrative Physiology 2009, 153:213-221.
63. Page M.M., Peters C.W., Staples J.F., Stuart J.A. Intracellular antioxidant enzymes are not globally upregulated during hibernation in the major oxidative tissues of the 13-lined ground squirrel Spermophilus tridecemlineatus. Comparative Biochemistry and Physiology Part A: Molecular and Integrative Physiology 2009, 152:115-122.
64. Petrović V.M., Milić B., Spasić M., Saicić Z. Copper-zinc containing and manganese containing superoxide dismutase in the ground squirrel/Citellus citellus/-the effect of hibernation. Free Radical Research Communications 1986, 1:339-346.
65. Petrović V.M., Saicić Z., Milić B., Spasić M., Radojicić R. Distribution of superoxide dismutase in the ground squirrel (Citellus citellus): effect of the hibernation and arousal. Comparative Biochemistry and Physiology B 1983, 75:699-700.
66. Poelchau M.F., Reynolds J.A., Denlinger D.L., Elsik C.G., Armbruster P.A. A de novo transcriptome of the Asian tiger mosquito, Aedes albopictus, to identify candidate transcripts for diapause preparation. BMC Genomics 2011, 12:619.
67. Post R.L., Hegyvary C., Kume S. Activation by adenosine triphosphate in the phosphorylation kinetics of sodium and potassium ion transport adenosine triphosphatase. Journal of Biological Chemistry 1972, 247:6530-6540.
68. Ragland G.J., Denlinger D.L., Hahn D.A. Mechanisms of suspended animation are revealed by transcript profiling of diapause in the flesh fly. Proceedings of the National Academy of Sciences of the United States of America 2010, 107:14909-14914.
69. Ren P., Lim C.S., Johnsen R., Albert P.S., Pilgrim D., Riddle D.L. Control of C. elegans larval development by neuronal expression of a TGF-beta homolog. Science 1996, 274:1389-1391.
70. Reynolds J.A., Poelchau M.F., Rahman Z., Armbruster P.A., Denlinger D.L. Transcript profiling reveals mechanisms for lipid conservation during diapause in the mosquito, Aedes albopictus. Journal of Insect Physiology 2012, 58:966-973.
71. Riddle D.L. The dauer larva. The nematode Caenorhabditis elegans 1988, 393-412. Cold Spring Harbor Laboratory Press, Plainview, New York.
72. Riddle D.L., Albert P.S. C. elegans II. C. elegans II 1997, 739-768. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY.
73. Rider M.H., Hussain N., Dilworth S.M., Storey J.M., Storey K.B. AMP-activated protein kinase and metabolic regulation in cold-hardy insects. Journal of Insect Physiology 2011, 57:1453-1462.
74. Robich R.M., Denlinger D.L. Diapause in the mosquito Culex pipiens evokes a metabolic switch from blood feeding to sugar gluttony. Proceedings of the National Academy of Sciences of the United States of America 2005, 102:15912-15917.
75. Schlaepfer W.W., Bunge R.P. Effects of calcium ion concentration on the degeneration of amputated axons in tissue culture. Journal of Cell Biology 1973, 59:456-470.
76. Schwartz C., Hampton M., Andrews M.T. Seasonal and regional differences in gene expression in the brain of a hibernating mammal. PLoS One 2013, 8:e58427.
77. Shaye D.D., Greenwald I. OrthoList: a compendium of C. elegans genes with human orthologs. PLoS One 2011, 6:e20085.
78. Sim C., Denlinger D.L. Insulin signaling and FOXO regulate the overwintering diapause of the mosquito Culex pipiens. Proceedings of the National Academy of Sciences of the United States of America 2008, 105:6777-6781.
79. Sim C., Denlinger D.L. Transcription profiling and regulation of fat metabolism genes in diapausing adults of the mosquito Culex pipiens. Physiological Genomics 2009, 39:202-209.
80. Sim C., Denlinger D.L. Catalase and superoxide dismutase-2 enhance survival and protect ovaries during overwintering diapause in the mosquito Culex pipiens. Journal of Insect Physiology 2011, 57:628-634.
81. Sim C., Denlinger D.L. Insulin signaling and the regulation of insect diapause. Frontiers in Physiology 2013, 4:189.
82. Skou J.C. The influence of some cations on an adenosine triphosphatase from peripheral nerves. Biochimica et Biophysica Acta 1957, 23:394-401.
83. Stegwee D., Kimmel E.C., de Boer J.A., Henstra S. Hormonal control of reversible degeneration of flight muscle in the Colorado potato beetle, Leptinotarsa decemlineata say (Coleoptera). Journal of Cell Biology 1963, 19:519-527.
84. Storey K.B., Storey J.M. Metabolic rate depression in animals: transcriptional and translational controls. Biological Reviews of the Cambridge Philosophical Society 2004, 79:207-233.
85. Syntichaki P., Xu K., Driscoll M., Tavernarakis N. Specific aspartyl and calpain proteases are required for neurodegeneration in C. elegans. Nature 2002, 419:939-944.
86. Tedeschi A., Bradke F. The DLK signalling pathway-a double-edged sword in neural development and regeneration. EMBO Reports 2013, 14:605-614.
87. Tymianski M., Charlton M.P., Carlen P.L., Tator C.H. Source specificity of early calcium neurotoxicity in cultured embryonic spinal neurons. Journal of Neuroscience 1993, 13:2085-2104.
88. Vanfleteren J.R., De Vreese A. Rate of aerobic metabolism and superoxide production rate potential in the nematode Caenorhabditis elegans. Journal of Experimental Zoology 1996, 274:93-100.
89. Wadsworth W.G., Riddle D.L. Developmental regulation of energy metabolism in Caenorhabditis elegans. Developmental Biology 1989, 132:167-173.
90. Wang J., Kim S.K. Global analysis of dauer gene expression in Caenorhabditis elegans. Development 2003, 130:1621-1634.
91. Xu K., Tavernarakis N., Driscoll M. Necrotic cell death in C. elegans requires the function of calreticulin and regulators of Ca(2+) release from the endoplasmic reticulum. Neuron 2001, 31:957-971.
92. Yan D., Wu Z., Chisholm A.D., Jin Y. The DLK-1 kinase promotes mRNA stability and local translation in C. elegans synapses and axon regeneration. Cell 2009, 138:1005-1018.
93. Yanik M.F., Cinar H., Cinar H.N., Chisholm A.D., Jin Y., Ben-Yakar A. Neurosurgery: functional regeneration after laser axotomy. Nature 2004, 432:822.
94. Zhang S., Arnadottir J., Keller C., Caldwell G.A., Yao C.A., Chalfie M. MEC-2 is recruited to the putative mechanosensory complex in C. elegans touch receptor neurons through its stomatin-like domain. Current Biology 2004, 14:1888-1896.
95. Zhao H.W., Christian S.L., Castillo M.R., Bult-Ito A., Drew K.L. Distribution of NMDA receptor subunit NR1 in arctic ground squirrel central nervous system. Journal of Chemical Neuroanatomy 2006, 32:196-207.
96. Zhao H.W., Ross A.P., Christian S.L., Buchholz J.N., Drew K.L. Decreased NR1 phosphorylation and decreased NMDAR function in hibernating Arctic ground squirrels. Journal of Neuroscience Research 2006, 84:291-298.