Structural plasticity in the developing visual system

Progress in Brain Research

Volumn 147, Issue SPEC. ISS., 2005, Pages 125-139

  Bence, Matt ^a   Levelt, Christiaan N ^a  

^a NETHERLANDS INSTITUTE FOR NEUROSCIENCE   (Netherlands)

Author keywords

cortex; critical period; deprivation; morphology; ocular dominance; plasticity; structural

Indexed keywords

BRAIN DERIVED NEUROTROPHIC FACTOR; CHONDROITIN SULFATE; PROTEOGLYCAN;

BINOCULAR VISION; CORTICAL SYNCHRONIZATION; DENDRITIC SPINE; DEVELOPMENTAL STAGE; EYE DOMINANCE; LONG TERM POTENTIATION; MOLECULAR BIOLOGY; MONOCULAR DEPRIVATION; NERVE CELL GROWTH; NERVE CELL PLASTICITY; NERVE FIBER GROWTH; NERVE PROJECTION; NERVOUS SYSTEM DEVELOPMENT; NONHUMAN; PRIORITY JOURNAL; REVIEW; SOMATOSENSORY CORTEX; SYNAPSE; VISUAL SYSTEM;

EID: 9644272560     PISSN: 00796123     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0079-6123(04)47010-1     Document Type: Review

References (99)

1. Ackermann M., Matus A. Activity-induced targeting of profilin and stabilization of dendritic spine morphology. Nat. Neurosci. 6:2003;1194-1200
2. Antonini A., Stryker M.P. Plasticity of geniculocortical afferents following brief or prolonged monocular occlusion in the cat. J. Comp. Neurol. 369:1996;64-82
3. Antonini A., Fagiolini M., Stryker M.P. Anatomical correlates of functional plasticity in mouse visual cortex. J. Neurosci. 19:1999;4388-4406
4. Baker R.E., Wolters P., Van Pelt J. Chronic blockade of glutamate-mediated bioelectric activity in long-term organotypic neocortical explants differentially effects pyramidal/non-pyramidal dendritic morphology. Dev. Brain Res. 104:1997;31-39
5. Bear M.F., Rittenhouse C.D. Molecular basis for induction of ocular dominance plasticity. J. Neurobiol. 41:1999;83-91
6. Borges S., Berry M. Preferential orientation of stellate cell dendrites in the visual cortex of the dark-reared rat. Brain Res. 1112:1976;141-147
7. Borges S., Berry M. The effects of dark rearing on the development of the visual cortex of the rat. J. Comp. Neurol. 180:1978;277-300
8. Benevento L.A., Bakkum B.W., Port J.D., Cohen R.S. The effects of dark-rearing on the electrophysiology of the rat visual cortex. Brain Res. 572:1992;198-207
9. Benevento L.A., Bakkum B.W., Cohen R.S. Gamma-Aminobutyric acid and somatostatin immunoreactivity in the visual cortex of normal and dark-reared rats. Brain Res. 689:1995;172-182
10. Bradbury E.J., Moon L.D., Popat R.J., King V.R., Bennett G.S., Patel P.N., Fawcett J.W., McMahon S.B. Chondroitinase ABC promotes functional recovery after spinal cord injury. Nature. 416:2002;636-640
11. Buffelli M., Burgess R.W., Feng G., Lobe C.G., Lichtman J.W., Sanes J.R. Genetic evidence that relative synaptic efficacy biases the outcome of synaptic competition. Nature. 424:2003;430-434
12. Campbell R.E., Tour O., Palmer A.E., Steinbach P.A., Baird G.S., Zacharias D.A., Tsien R.Y. A monomeric red fluorescent protein. Proc. Natl. Acad. Sci. USA. 99:2002;7877-7882
13. Casagrande V.A., Xu X., Sary G. Static and dynamic views of visual cortical organization. Prog. Brain Res. 136:2002;389-408
14. Cline H.T. Dendritic arbor development and synaptogenesis. Curr. Opin. Neurobiol. 11:2001;118-126
15. Crair M.C., Horton J.C., Antonini A., Stryker M.P. Emergence of ocular dominance columns in cat visual cortex by 2 weeks of age. J. Comp. Neurol. 430:2001;235-249.. Related Articles, Links
16. Crowley J.C., Katz L.C. Development of ocular dominance columns in the absence of retinal input. Nat. Neurosci. 2:1999;1125-1130
17. Crowley J.C., Katz L.C. Early development of ocular dominance columns. Science. 290:2000;1321-1324
18. De Paola V., Arber S., Caroni P. AMPA receptors regulate dynamic equilibrium of presynaptic terminals in mature hippocampal networks. Nat. Neurosci. 6:2003;491-500
19. Engert F., Bonhoeffer T. Dendritic spine changes associated with hippocampal long-term synaptic plasticity. Nature. 399:(6731):1999;66-70
20. Fagiolini M., Fritschy J.M., Low K., Mohler H., Rudolph U., Hensch T.K. Specific GABAA circuits for visual cortical plasticity. Science. 303:2004;1681-1683
21. Feng G., Mellor R.H., Bernstein M., Keller-Peck C., Nguyen Q.T., Wallace M., Nerbonne J.M., Lichtman J.W., Sanes J.R. Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP. Neuron. 28:2000a;41-51
22. Feng J., Yan Z., Ferreira A., Tomizawa K., Liauw J.A., Zhuo M., Allen P.B., Ouimet C.C., Greengard P. Spinophilin regulates the formation and function of dendritic spines. Proc. Natl. Acad. Sci. U. S. A. 97:2000b;9287-9292
23. Fiala J.C., Allwardt B., Harris K.M. Dendritic spines do not split during hippocampal LTP or maturation. Nat Neurosci. 5:(4):2002;297-298
24. Fifkova E. The effect of unilateral deprivation on visual centers in rats. J. Comp. Neurol. 140:1970;431-438
25. Fink C.C., Bayer K.U., Myers J.W., Ferrell J.E., Jr., Schulman H., Meyer T. Selective regulation of neurite extension and synapse formation by the beta but not the alpha isoform of CaMKII. Neuron. 39:(2):2003;283-297
26. Fischer M., Kaech S., Wagner U., Brinkhaus H., Matus A. Glutamate receptors regulate actin-based plasticity in dendritic spines. Nat. Neurosci. 3:2000;887-894
27. Freire M. Effects of dark rearing on dendritic spines in layer IV of the mouse visual cortex. A quantitative electron microscopical study. J. Anat. 126:1978;193-201
28. Frey U., Morris R.G. Synaptic tagging and long-term potentiation. Nature. 385:1997;533-536
29. Grutzendler J., Kasthuri N., Gan W.B. Long-term dendritic spine stability in the adult cortex. Nature. 420:2002;812-816
30. Hartmann M., Heumann R., Lessmann V. Synaptic secretion of BDNF after high-frequency stimulation of glutamatergic synapses. EMBO J. 20:(21):2001;5887-5897
31. Hayashi Y., Shi S.H., Esteban J.A., Piccini A., Poncer J.C., Malinow R. Driving AMPA receptors into synapses by LTP and CaMKII: requirement for GluR1 and PDZ domain interaction. Science. 287:2000;2262-2267
32. Henkemeyer M., Itkis O.S., Ngo M., Hickmott P.W., Ethell I.M. Multiple EphB receptor tyrosine kinases shape dendritic spines in the hippocampus. J. Cell Biol. 163:(6):2003;1313-1326
33. Hensch T.K., Stryker M.P. Columnar architecture sculpted by GABA circuits in developing cat visual cortex. Science. 303:2004;1678-1681
34. Hensch T.K., Fagiolini M., Mataga N., Stryker M.P., Baekkeskov S., Kash S.F. Local GABA circuit control of experience-dependent plasticity in developing visual cortex. Science. 282:1998;1504-1508
35. Heynen A.J., Yoon B.J., Liu C.H., Chung H.J., Huganir R.L., Bear M.F. Molecular mechanism for loss of visual cortical responsiveness following brief monocular deprivation. Nat. Neurosci. 6:2003;854-862
36. Hua J.Y., Smith S.J. Neural activity and the dynamics of central nervous system development. Nat. Neurosci. 7:2004;327-332
37. Huang Z.J., Kirkwood A., Pizzorusso T., Porciatti V., Morales B., Bear M.F., Maffei L., Tonegawa S. BDNF regulates the maturation of inhibition and the critical period of plasticity in mouse visual cortex. Cell. 98:1999;739-755
38. Huang Z.J., Yu W., Lovett C., Tonegawa S. Cre/loxP recombination- activated neuronal markers in mouse neocortex and hippocampus. Genesis. 32:2002;209-217
39. Hubel D.H., Wiesel T.N., LeVay S. Plasticity of ocular dominance columns in monkey striate cortex. Philos. Trans. R. Soc. Lond. B. Biol. Sci. 278:1977;377-409
40. Huttenlocher P.R., Dabholkar A.S. Regional differences in synaptogenesis in human cerebral cortex. J Comp. Neurol. 387:1997;167-178
41. Isaac J. Protein phosphatase 1 and LTD: synapses are the architects of depression. Neuron. 32:2001;963-966
42. Iwai Y., Fagiolini M., Obata K., Hensch T.K. Rapid critical period induction by tonic inhibition in visual cortex. J. Neurosci. 23:2003;6695-6702
43. Jourdain P., Fukunaga K., Muller D. Calcium/calmodulin-dependent protein kinase II contributes to activity-dependent filopodia growth and spine formation. J. Neurosci. 23:2003;10645-10649
44. Katz L.C., Shatz C.J. Synaptic activity and the construction of cortical circuits. Science. 274:1996;1133-1138
45. Kirov S.A., Harris K.M. Dendrites are more spiny on mature hippocampal neurons when synapses are inactivated. Nat. Neurosci. 2:1999;878-883
46. Kossel A., Lowel S., Bolz J. Relationships between dendritic fields and functional architecture in striate cortex of normal and visually deprived cats. J. Neurosci. 15:1995;3913-3926
47. Kozak M. Alternative ways to think about mRNA sequences and proteins that appear to promote internal initiation of translation. Gene. 318:2003;1-23
48. Lendvai B., Stern E.A., Chen B., Svoboda K. Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo. Nature. 404:2000;876-881
49. Liao D., Scannevin R.H., Huganir R. Activation of silent synapses by rapid activity-dependent synaptic recruitment of AMPA receptors. J. Neurosci. 21:(16):2001;6008-6017
50. Lisman J.E., Zhabotinsky A.M. A model of synaptic memory: a CaMKII/PP1 switch that potentiates transmission by organizing an AMPA receptor anchoring assembly. Neuron. 31:(2):2001;191-201
51. Lu W., Man H., Ju W., Trimble W.S., MacDonald J.F., Wang Y.T. Activation of synaptic NMDA receptors induces membrane insertion of new AMPA receptors and LTP in cultured hippocampal neurons. Neuron. 29:2001;243-254
52. Lund J.S., Holbach S.M., Chung W.W. Postnatal development of thalamic recipient neurons in the monkey striate cortex: II. Influence of afferent driving on spine acquisition and dendritic growth of layer 4C spiny stellate neurons. J. Comp. Neurol. 309:1991;129-140
53. Majewska A., Sur M. Motility of dendritic spines in visual cortex in vivo: changes during the critical period and effects of visual deprivation. Proc. Natl. Acad. Sci. USA. 100:2003;16024-16029
54. Maletic-Savatic M., Malinow R., Svoboda K. Rapid dendritic morphogenesis in CA1 hippocampal dendrites induced by synaptic activity. Science. 283:1999;1923-1927
55. McAllister A.K., Katz L.C., Lo D.C. Regulation of cortical dendritic growth requires activity. Neuron. 17:1996;1057-1064
56. McAllister A.K. Cellular and molecular mechanisms of dendrite growth. Cereb Cortex. 10:2000;963-973
57. McKinney R.A., Capogna M., Durr R., Gahwiler B.H. Miniature synaptic events maintain dendritic spines via AMPA receptor activation. Nat. Neurosci. 2:1999;44-49
58. Messaoudi E., Ying S.W., Kanhema T., Croll S.D., Bramham C.R. Brain-derived neurotrophic factor triggers transcription-dependent, late phase long-term potentiation in vivo. J. Neurosci. 22:(17):2002;7453-7461
59. Miyawaki A. Green fluorescent protein-like proteins in reef Anthozoa animals. Cell Struct. Funct. 27:2002;343-347
60. Mizrahi A., Crowley J.C., Shtoyerman E., Katz L.C. High-resolution in vivo imaging of hippocampal dendrites and spines. J. Neurosci. 24:(13):2004;3147-3151
61. Morel M.P., Dusart I., Sotelo C. Sprouting of adult Purkinje cell axons in lesioned mouse cerebellum: "non-permissive" versus "permissive" environment. J. Neurocytol. 31:2002;633-647
62. Mower G.D., Christen W.G., Caplan C.J. Brief visual experience eliminates plasticity in the cat visual cortex. Science. 221:1983;178-180
63. Muller D., Nikonenko I. Dynamic presynaptic varicosities: a role in activity-dependent synaptogenesis. Trends Neurosci. 26:2003;573-575
64. Mulkey R.M., Endo S., Shenolikar S., Malenka R.C. Involvement of a calcineurin/inhibitor-1 phosphatase cascade in hippocampal long-term depression. Nature. 369:1994;486-488
65. Nakayama A.Y., Luo L. Intracellular signaling pathways that regulate dendritic spine morphogenesis. Hippocampus. 10:2000;582-586
66. Niell C.M., Meyer M.P., Smith S.J. In vivo imaging of synapse formation on a growing dendritic arbor. Nat. Neurosci. 7:2004;254-260
67. Nikonenko I., Jourdain P., Muller D. Presynaptic remodeling contributes to activity-dependent synaptogenesis. J. Neurosci. 23:2003;8498-8505
68. Ostroff L.E., Fiala J.C., Allwardt B., Harris K.M. Polyribosomes redistribute from dendritic shafts into spines with enlarged synapses during LTP in developing rat hippocampal slices. Neuron. 35:(3):2002;535-545
69. Pak D.T., Sheng M. Targeted protein degradation and synapse remodeling by an inducible protein kinase. Science. 302:2003;1368-1373
70. Passafaro M., Nakagawa T., Sala C., Sheng M. Induction of dendritic spines by an extracellular domain of AMPA receptor subunit GluR2. Nature. 424:2003;677-681
71. Pizzorusso T., Medini P., Berardi N., Chierzi S., Fawcett J.W., Maffei L. Reactivation of ocular dominance plasticity in the adult visual cortex. Science. 298:2002;1248-1251
72. Ramakers G.J. Rho proteins, mental retardation and the cellular basis of cognition. Trends Neurosci. 2:2002;191-199
73. Ruiz-Marcos A., Valverde F. The temporal evolution of the distribution of dendritic spines in the visual cortex of normal and dark raised mice. Exp. Brain Res. 8:(3):1969;284-294
74. Ruthazer E.S., Akerman C.J., Cline H.T. Control of axon branch dynamics by correlated activity in vivo. Science. 301:2003;66-70
75. Saghatelyan A.K., Dityatev A., Schmidt S., Schuster T., Bartsch U., Schachner M. Reduced perisomatic inhibition, increased excitatory transmission, and impaired long-term potentiation in mice deficient for the extracellular matrix glycoprotein tenascin-R. Mol. Cell. Neurosci. 17:(1):2001;226-240
76. Sala C. Molecular regulation of dendritic spine shape and function. Neurosignals. 11:2002;213-223
77. Sawtell N.B., Frenkel M.Y., Philpot B.D., Nakazawa K., Tonegawa S., Bear M.F. NMDA receptor-dependent ocular dominance plasticity in adult visual cortex. Neuron. 38:(6):2003;977-985
78. Scheiffele P. Cell-cell signaling during synapse formation in the CNS. Annu. Rev. Neurosci. 26:2003;485-508
79. Shatz C.J., Stryker M.P. Ocular dominance in layer IV of the cat's visual cortex and the effects of monocular deprivation. J. Physiol. 281:1978;267-283
80. Sherman S.M., Spear P.D. Organization of visual pathways in normal and visually deprived cats. Physiol. Rev. 62:1982;738-855
81. Shi S.H., Hayashi Y., Petralia R.S., Zaman S.H., Wenthold R.J., Svoboda K., Malinow R. Rapid spine delivery and redistribution of AMPA receptors after synaptic NMDA receptor activation. Science. 284:(5421):1999;1811-1816
82. Smith E.L., Bennett M.J., Harwerth R.S., Crawford M.L. Binocularity in kittens reared with optically induced squint. Science. 204:1970;875-877
83. Tashiro A., Dunaevsky A., Blazeski R., Mason C.A., Yuste R. Regulation of hippocampal mossy fiber filopodial motility by kainate receptors: a two-step model of synaptogenesis. Neuron. 38:2003;773-784
84. Theer P., Hasan M.T., Denk W. Two-photon imaging to a depth of 1000 microm in living brains by use of a Ti: Al2O3 regenerative amplifier. Opt Lett. 28:2003;1022-1024
85. Tieman S.B. Morphological changes in the geniculocortical pathway associated with monocular deprivation. Ann. N Y Acad. Sci. 627:1991;212-230
86. Tieman S.B., Zec N., Tieman D.G. Dark-rearing fails to affect the basal dendritic fields of layer 3 pyramidal cells in the kitten's visual cortex. Dev. Brain Res. 84:1995;39-45
87. Trachtenberg J.T., Trepel C., Stryker M.P. Rapid extragranular plasticity in the absence of thalamocortical plasticity in the developing primary visual cortex. Science. 287:2000;2029-2032
88. Trachtenberg J.T., Stryker M.P. Rapid anatomical plasticity of horizontal connections in the developing visual cortex. J. Neurosci. 21:2001;3476-3482
89. Trachtenberg J.T., Chen B.E., Knott G.W., Feng G., Sanes J.R., Welker E., Svoboda K. Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex. Nature. 420:2002;788-794
90. Tropea D., Caleo M., Maffei L. Synergistic effects of brain-derived neurotrophic factor and chondroitinase ABC on retinal fiber sprouting after denervation of the superior colliculus in adult rats. J. Neurosci. 23:2003;7034-7044
91. Turrigiano G.G., Nelson S.B. Homeostatic plasticity in the developing nervous system. Nat. Rev. Neurosci. 5:2004;97-107
92. Valverde F. Rate and extent of recovery from dark rearing in the visual cortex of the mouse. Brain Res. 33:1971;1-11
93. Vaughn J.E. Fine structure of synaptogenesis in the vertebrate central nervous system. Synapse. 3:1989;255-285
94. Wiesel T.N., Hubel D.H. Single cell responses in striate cortex of kittens deprived of vision in one eye. J. Neurophysiol. 26:1963;1003-1017
95. Wise S.P., Fleshman J.W., Jr., Jones E.G. Maturation of pyramidal cell form in relation to developing afferent and efferent connection of rat somatic sensory cortex. Neuroscience. 4:1979;1275-1297
96. Wong R.O., Ghosh A. Activity-dependent regulation of dendritic growth and patterning. Nat. Rev. Neurosci. 3:2002;803-812
97. Yuste R., Bonhoeffer T. Genesis of dendritic spines: insights from ultrastructural and imaging studies. Nat. Rev. Neurosci. 5:(1):2004;24-34
98. Zecevic N., Rakic P. Synaptogenesis in monkey somatosensory cortex. Cereb Cortex. 1:1991;510-523
99. Zeng H., Chattarji S., Barbarosie M., Rondi-Reig L., Philpot B.D., Miyakawa T., Bear M.F., Tonegawa S. Forebrain-specific calcineurin knockout selectively impairs bidirectional synaptic plasticity and working/episodic-like memory. Cell. 107:2001;617-629