Cellular and molecular bases of neuroplasticity: Brainstem effects after cochlear damage

Acta Oto-Laryngologica

Volumn 130, Issue 3, 2010, Pages 318-325

  Gil Loyzaga, Pablo ^a   Carricondo, Francisco ^a,b   Bartolomé, Maria V ^a   Iglesias, Mari C ^a,b   Rodríguez, Fernando ^a,b   Poch Broto, Joaquin ^a,b  

^a UNIVERSIDAD COMPLUTENSE DE MADRID   (Spain)

^b HOSPITAL CLÍNICO SAN CARLOS   (Spain)

Author keywords

Auditory system; Brainstem; Cochlea; Cochlear nuclei; Neuroplasticity

Indexed keywords

NEUROMODULIN;

BRAIN STEM; CELL ULTRASTRUCTURE; COCHLEA INJURY; COCHLEA PROSTHESIS; COCHLEAR NERVE; COCHLEAR NUCLEUS; EDEMA; HEARING AID; HUMAN; LEARNING; MEMORY; NERVE CELL NETWORK; NERVE CELL PLASTICITY; NERVE DEGENERATION; NERVE ENDING; NERVE INJURY; NERVE REGENERATION; NERVE TRACT; NONHUMAN; PRIORITY JOURNAL; PROTEIN EXPRESSION; REVIEW; SENSORY NERVE CELL; SYNAPTIC TRANSMISSION; SYNAPTOGENESIS;

EID: 77149132207     PISSN: 00016489     EISSN: 16512553     Source Type: Journal    
DOI: 10.3109/00016480903127468     Document Type: Review

References (74)

1. Díaz Arribas MJ, Pardo-Hervás P, Tabares-Lavado M, Rios-Lago M, Maestú F. [Plasticity of the central nervous system and treatment strategies for sensory and motor reprogram: comparison between two cases of cerebrovascular disease in the middle cerebral artery terrritory.]. Rev Neurol 2006;42:153-8. (in Spanish)
2. Shimojo S, Sams L. Sensory modalities are not separate modalities: plasticity and interactions. Curr Opin Neurobiol 2001;11:505-9.
3. Bergado-Rosado JA, Almaguer-Melian W. Cellular mechanisms of neuroplasticity. Rev Neurol 2000;31:1074-95.
4. Gil-Loyzaga P. Biological bases of neuroplasticity: in vivo and in vitro studies. Interest for the auditory system. Audiological Medicine 2009;7:3-10.
5. Nitsche MA, Liebetanz D, Paulus W, Tergau F. Pharmacological characterisation and modulation of neuroplasticity in humans. Curr Neuropharmacol 2005;3:217-29.
6. Syka J. Plastic changes in the central auditory system after hearing loss, restoration of function, and during learning. Physiol Rev 2002;82:601-36.
7. Gil-Loyzaga P. Neuroplasticity in the auditory system. Eur Rev ENT 2005;126:203-8.
8. Gil-Loyzaga P, Iglesias MC, Carricondo F, Bartolome M, Rodríguez F, Poch-Broto J. Cochlear nuclei neuroplasticity after auditory nerve and cochlea removal. Audiological Medicine 2009;7:29-39.
9. Deacon TW. Prefrontal cortex and symbol learning: why a brain capable of language evolved only once. In: Velichkovsky BM, Rumbaugh DM, edtiors. Communicating meaning: the evolution and development of language. New York: LEA; 1996. p. 103-38.
10. Irvine DR. Auditory cortical neuroplasticity: does it provide evidence for cognitive processing in the auditory cortex? Hear Res 2007;229:158-70.
11. Moller AR. Symptoms and signs caused by neural plasticity. Neurol Res 2001;23:565-72.
12. Bartels H, Staal MJ, Albers FWJ. Tinnitus and neural plasticity of the brain. Otol Neurotol 2007;28:178-84.
13. Cacace AT. Expanding the biological bases of tinnitus: cross-modal origins and the role of neuroplasticity. Hear Res 2003;175:112-32.
14. Jin YM, Godfrey DA. Effects of cochlear ablation on muscarinic acetylcholine receptor binding in the rat cochlear nucleus. J Neurosci Res 2006;83:157-66.
15. Barbacid M. Neurotrophic factors and their receptors. Curr Opin Cell Biol 1995;7:148-55.
16. Levi-Montalcini R. Developmental neurobiology and the natural history of nerve growth factor. Annu Rev Neurosci 1982;5:341-62.
17. Korsching S. The neurotrophic factor concept: a reexamination. J Neurosci 1993;13:2739-48.
18. Chao MV, Hempstead BL. p75 and Trk: a two-receptor system. TINS. 1995;18:321-6.
19. Pirvola U, Hallböök F, Xing-Qun L, Virkkala J, Saarma M, Ylikoski J. Expression of neurotrophins and Trk receptors in the developing, adult, and regenerating avian cochlea. J Neurobiol 1997;33:1019-33.
20. Ditlevsen DK, Povlsen GK, Berezin V, Boek E. NCAM-induced intracellular signaling revisited. J Neurosci Res 2008;86:727-43.
21. Gil-Loyzaga P, Pujol R. Neurotransmitters and neuroplasticity during cochlear development: in vivo and in vitro studies. Audiological Medicine 2009;7:11-21.
22. Haberny KA, Paule MG, Scallet AC, Sistare FD, Lester DS, Haniq JP, et al. Ontogeny of the N-methyl-D-aspartate (NMDA) receptor system and susceptibility to neurotoxicity. Toxicol Sci 2002;68:9-17.
23. Emerit MB, Riad M, Hamon M. Trophic effects of neuro-transmitters during brain maturation. Biol Neonate 1992;62:193-201.
24. Castro Soubriet F. Moléculas quimiotrópicas como mecanismo de orientación del crecimiento axonal y de la migración neuronal durante el desarrollo del sistema nervioso de los mamíferos. Rev Neurol 2001;33:54-68.
25. Brors D, Aletsee C, Dazert S, Huverstuhl J, Ryan AF, Bodmer D. Clostridium difficile toxin B, an inhibitor of the small GT Pases Rho, Racand Cdc42, influences spiral ganglion neurite outgrowth. Acta Otolaryngol 2003;123:20-5.
26. Toyama K, Komatsu Y, Yamamoto N, Kurotami T, Yamada K. In vitro approach to visual cortical development and plasticity. Neurosci Res 1991;12:57-71.
27. Bufill E, Carbonell E. Are symbolic behaviour and neuro-plasticity an example of gene-culture coevolution? Rev Neurol 2004;39:48-55.
28. Letourneau PC. Regulation of nerve flber elongation during embryogenesis. In: Greennough WT, Juraska JM, editors. Developmental neuropsychobiology. Orlando, FL: Academic Press; 1986. p. 33-71.
29. Portera-Cailliau C, Yuste R. On the function of dendritic filopodia. Rev Neurol 2001;33:1158-66.
30. Illing RB, Reisch A. Specific plasticity responses to unilaterally decreased or increased hearing intensity in the adult cochlear nucleus and beyond. Hear Res 2006;216: 189-97.
31. Rubel EW, Hyson RL, Durham D. Afferent regulation of neurons in the brain stem auditory system. J Neurobiol 1990;21:169-96.
32. Kraus KS, Illing RB. Cell death or survival: molecular and connectional conditions for olivocochlear neurons after axotomy. Neuroscience 2005;134:467-81.
33. Morest DK, Kim J, Bohne BA. Neuronal and transneuronal degeneration of auditory axons in the brainstem after cochlear lesions in the chinchilla: cochleotopic and noncochleotopic patterns. Hear Res 1997;103:151-68.
34. Gil-Loyzaga P, Pujol R. Synaptophysin in the developing cochlea. Int J Dev Neurosci 1988;6:155-60.
35. Südh of TC. The synaptic vesicle cycle: a cascade of protein-protein interactions. Nature 1995;375:645-53.
36. Jahn R, Schiebler W, Ouimet C, Greengard P. A 38,000-dalton membrane protein (p38) present in synaptic vesicles. Proc Natl Acad Sci U S A 1985;82:4137-41.
37. Knaus P, Betz H, Rehm H. Expression of synaptophysin during postnatal development of the mouse brain. J Neurochem 1986;47:1302-4.
38. Navone F, Jahn R, Di Gioia G, Stukenbrok H, Greengard P, De Camilli P. Protein p38: an integral membrane protein specific for small vesicles of neurons and neuroendocrine cells. J Cell Biol 1986;103:2511-27.
39. Wiedermann B, Franke WW, Kuhn C, Moll R, Gould VE. Synaptophysin: a marker protein for neuroendocrine cells and neoplasms. Proc Natl Acad Sci U S A 1986;83:3500-4.
40. Thomas L, Hartung K, Langosch D, Rehm H, Bamberg E, Franke WW, et al. Identification of synaptophysin as a hexameric channel protein of the synaptic vesicle membrane. Science 1988;242:1050-3.
41. Johnston PA, Jahn R, Südh of TC. Transmembrane topography and evolutionary conservation of synaptophysin. J Biol Chem 1989;264:1268-73.
42. Wiedenmann B, Franke WW. Identification and localization of synaptophysin, an integral membrane glycoprotein of Mr 38,000 characteristic of presynaptic vesicles. Cell 1985;41:1017-28.
43. Rehm H, Wiedenmann B, Betz H. Molecular characterization of synaptophysin, a major calcium-binding protein of the synaptic vesicle membrane. EMBO J 1986;5:535-41.
44. Korematsu K, Goto S, Nagahiro S, Ushio Y. Changes of immunoreactivity for synaptophysin ('protein p38') following a transient cerebral ischemia in the rat striatum. Brain Res 1993;616:320-4.
45. Bartolomé M, Ibáñez MA, López-Sánchez JG, Merchán-Pérez A, Gil-Loyzaga P. Synaptophysin immunoreactivity in the cochlear nuclei of mammals: a comparative study. ORL J Otorhinolaryngol Relat Spec 1993;55:317-32.
46. Benson CG, Gross JS, Suneja SK, Potashner SJ. Synaptophysin immunoreactivity in the cochlear nucleus after uni-lateral cochlear or ossicular removal. Synapse 1997;25:243-57.
47. Lorente de Nó R. The primary acoustic nuclei. New York: Raven Press; 1981.
48. Verhhagen J, Van Hooff COM, Edwards PM, De Graan PNE, Oestreicher AB, Schotman P, et al. The kinase C substrate protein B-50 and axonal regeneration. Brain Res Bull 1986;17:737-41.
49. Lasiter PS, Kachele DL. Postnatal development of protein P-38 ('synaptophysin') immunoreactivity in pontine and medullary gustatory zones of rat. Dev Brain Res 1989;48:27-33.
50. Bergmann M, Schuster T, Grabs D, Marquèze-Pouey B, Betz H, Traurig H, et al. Synaptophysin and synaptoporin expression in the developing rat olfactory system. Dev Brain Res 1993;74:235-44.
51. Ovtscharoff W, Bergmann M, Marquèze-Pouey B, Knaus P, Betz H, Grabs D, et al. Ontogeny of synaptophysin and synaptoporin in the central nervous system: differential expression in striatal neurons and their afferents during development. Dev Brain Res 1993;72: 219-25.
52. Illing RB, Horváth M. Re-emergence of GAP-43 in cochlear nucleus and superior olive following cochlear ablation in the rat. Neurosci Lett 1995;194:9-12.
53. Illing RB, Horvatz M, Laszig R. Plasticity of the auditory brainstem: effects of cochlear ablation on GAP-43 immunoreactivity in the rat. J Comp Neurol 1997;382:116-38.
54. Merchán-Pérez A, Bartolomé M, Ibáñez MA, Gil-Loyzaga P. Expression of GAP-43 in growing efferent flbers during cochlear development. ORL J Otorhinolaryngol Relat Spec 1993;55:208-10.
55. Illing RB, Cao QL, Forster CR, Laszig R. Auditory brainstem: development and plasticity of GAP-43 mRNA expression in the rat. J Comp Neurol 1999;412:353-72.
56. Bartolome MV, Ibanez A, Gil-Loyzaga P. Transitional expression of OX-2 and GAP-43 glycoproteins in developing cochlear nerve flbers. Histol Histopathol 2002;17:83-95.
57. Skene JH, Jacobson RD, Snipes GJ, McGuire CB, Norden JJ, Freeman JA. A protein induced during nerve growth (GAP-43) is a major component of growth-cone membranes. Science 1986;233:783-6.
58. Benowitz LI, Perrone-Bizzosero NI. The relationship of GAP-43 to the development and plasticity of synaptic connections. Ann N Y Acad Sci 1991;627:58-74.
59. Osen KK. Cytoarchitecture of the cochlear nuclei in the cat. J Comp Neurol 1969;136:453-84.
60. Brawer JR, Morest DK, Kane EC. The neuronal architecture of the cochlear nucleus of the cat. J Comp Neurol 1974;155:251-300.
61. Hackney CM, Osen KK, Kolston J. Anatomy of the cochlear nuclear complex of guinea pig. Anat Embryol (Berl) 1990;182:123-49.
62. Mostafapour SP, Cochran SL, del Puerto NM, Rubel EW. Patterns of cell death in mouse anteroventral cochlear nucleus neurons after unilateral cochlea removal. J Comp Neurol 2000;426:561-71.
63. Cant NB, Morest DK. Organization of the neurons in the anterior division of the anteroventral cochlear nucleus of the cat. Light-microscopic observations. Neuroscience 1979;4: 1909-23.
64. Shore SE, Godfrey DA, Helfert RH, Altschuler RA, Bledsoe SC Jr. Connections between the cochlear nuclei in guinea pig. Hear Res 1992;62:16-26.
65. Ryan AF, Keithley EM, Wang ZX, Schwartz IR. Collaterals from lateral and medial olivocochlear efferent neurons innervate different regions of the cochlear nucleus and adjacent brainstem. J Comp Neurol 1990;300:572-82.
66. Shore SE, Helfert RH, Bledsoe SC Jr, Altschuler RA, Godfrey DA. Descending projections to the dorsal and ventral divisions of the cochlear nucleus in guinea pig. Hear Res 1991;52:255-68.
67. Fuentes-Santamaría V, Alvarado JC, Henkel CK, Brunso-Bechtold JK. Cochlear ablation in adult ferrets results in changes in insulin-like growth factor-1 and synaptophysin immunostaining in the cochlear nucleus. Neuroscience 2007;148:1033-47.
68. D'Sa C, Gross J, Francone VP, Morest DK. Plasticity of synaptic endings in the cochlear nucleus following noise-induced hearing loss is facilitated in the adult FGF2 over-expressor mouse. Eur J Neurosci 2007;26:666-80.
69. Holt AG, Asako M, Lomax CA, MacDonald J, Tong L, Lomax MI, et al. Deafness-related plasticity in the inferior colliculus: gene expression profiling following removal of peripheral activity. J Neurochem 2005;93:1069-86.
70. Mossop J, Wilson M, Caspary D, Moore D. Down-regulation of inhibition following unilateral deafening. Hear Res 2000;147:183-7.
71. Pavon N, Vidal L, Blanco L, Alvarez-Fonseca P, Torres-Montoya A, Lorigados L, et al. Factores que desencadenan la muerte neuronal en enfermedades neurodegenerativas. Rev Neurol 1998;26:544-60.
72. Durham D, Park DL, Girod DA. Central nervous system plasticity during hair cell loss and regeneration. Hear Res 2000;147:145-59.
73. d'Aldin CG, Ruel J, Assié R, Pujol R, Puel JL. Implication of NMDA type glutamate receptors in neural regeneration and neoformation of synapses after excitotoxic injury in the guinea pig cochlea. Int J Dev Neurosci 1997;15:619-29.
74. Gil-Loyzaga P. Neuroplasticity in the auditory system. Rev Laryngol Otol Rhinol (Bord) 2005;126:203-7.