Plasticity and specificity of cortical processing networks

Trends in Neurosciences

Volumn 29, Issue 6, 2006, Pages 323-329

  Majewska, Ania K ^a   Sur, Mriganka ^b  

^a UNIVERSITY OF ROCHESTER MEDICAL CENTER   (United States)

^b MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASSOCIATION; BRAIN DEVELOPMENT; BRAIN FUNCTION; CELL SPECIFICITY; CELL TYPE; EXPERIENCE; GENE EXPRESSION; MEDICAL INFORMATION; MOLECULAR MECHANICS; NERVE CELL NETWORK; NERVE CELL PLASTICITY; NERVE FUNCTION; NONHUMAN; POSTSYNAPTIC MEMBRANE; PRIORITY JOURNAL; REVIEW; SYNAPTIC TRANSMISSION; VISION; VISUAL CORTEX; VISUAL STIMULATION;

ANIMALS; CEREBRAL CORTEX; HUMANS; MODELS, NEUROLOGICAL; NERVE NET; NEURONAL PLASTICITY; NEURONS; SYNAPSES;

EID: 33745127665     PISSN: 01662236     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tins.2006.04.002     Document Type: Review

References (88)

1. Lopez-Bendito G., and Molnar Z. Thalamocortical development: how are we going to get there?. Nat. Rev. Neurosci. 4 (2003) 276-289
2. Sur M., and Rubenstein J.L.R. Patterning and plasticity of the cerebral cortex. Science 310 (2005) 805-810
3. Polleux F. Genetic mechanisms specifying cortical connectivity: let's make some projections together. Neuron 46 (2005) 395-400
4. Sincich L.C., and Horton J.C. The circuitry of V1 and V2: integration of color, form, and motion. Annu. Rev. Neurosci. 28 (2005) 303-326
5. Yu H., et al. The coordinated mapping of visual space and response features in visual cortex. Neuron 47 (2005) 267-280
6. Crowley J.C., and Katz L.C. Early development of ocular dominance columns. Science 290 (2000) 1321-1324
7. Sur M., and Leamey C. Development and plasticity of cortical areas and networks. Nat. Rev. Neurosci. 2 (2001) 251-262
8. Crowley J.C., and Katz L.C. Development of ocular dominance columns in the absence of retinal input. Nat. Neurosci. 2 (1999) 1125-1130
9. Newton, J. et al. (2005) Intrinsic signal optical imaging reveals the distinct effects of thalamic and cortical mechanisms on patterning and arealization in V1 and V2 of ephrin A2/A5 knock-out mice. Program No. 300.3. In 2005 Abstract Viewer and Itinerary Planner, Society for Neuroscience Online (http://sfn.scholarone.com/)
10. Cang J., et al. Ephrin-As guide the formation of functional maps in the visual cortex. Neuron 48 (2005) 577-589
11. Portera-Cailliau C., et al. Diverse modes of axon elaboration in the developing neocortex. PLoS Biol. 3 (2005) e272
12. Cang J., et al. Development of precise maps in visual cortex requires patterned spontaneous activity in the retina. Neuron 48 (2005) 797-809
13. Bence M., and Levelt C.N. Structural plasticity in the developing visual system. Prog. Brain Res. 147 (2005) 125-139
14. Trachtenberg J.T., et al. Rapid extragranular plasticity in the absence of thalamocortical plasticity in the developing primary visual cortex. Science 287 (2000) 2029-2032
15. Krahe T.E., et al. Protein synthesis-independent plasticity mediates rapid and precise recovery of deprived eye responses. Neuron 48 (2005) 329-343
16. Yu, H. et al. (2005) Rearrangement of dendritic spines during short term monocular deprivation in the primary visual cortex of the ferret in vivo. Program No. 714.8. In 2005 Abstract Viewer and Itinerary Planner, Society for Neuroscience Online (http://sfn.scholarone.com/)
17. Bear M.F. Bidirectional synaptic plasticity: from theory to reality. Philos. Trans. R. Soc. Lond. B Biol. Sci. 358 (2003) 649-655
18. Yuste R., et al. From form to function: calcium compartmentalization in dendritic spines. Nat. Neurosci. 3 (2000) 653-659
19. Fischer M., et al. Rapid actin-based plasticity in dendritic spines. Neuron 20 (1998) 847-854
20. Dunaevsky A., et al. Developmental regulation of spine motility in the mammalian central nervous system. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 13438-13443
21. Lendvai B., et al. Experience-dependent plasticity of dendritic spines in the developing rat barrel cortex in vivo. Nature 404 (2000) 876-881
22. Fischer M., et al. Glutamate receptors regulate actin-based plasticity in dendritic spines. Nat. Neurosci. 3 (2000) 887-894
23. Korkotian E., and Segal M. Regulation of dendritic spine motility in cultured hippocampal neurons. J. Neurosci. 21 (2001) 6115-6124
24. Oray S., et al. Effects of synaptic activity on dendritic spine motility of developing cortical layer V pyramidal neurons. Cereb. Cortex 16 (2006) 730-741
25. Hayashi Y., and Majewska A. Dendritic spine geometry: functional implication and regulation. Neuron 46 (2005) 529-532
26. Matsuzaki M., et al. Structural basis of long-term potentiation in single dendritic spines. Nature 429 (2004) 761-766
27. Okamoto K., et al. Rapid and persistent modulation of actin dynamics regulates postsynaptic reorganization underlying bidirectional plasticity. Nat. Neurosci. 7 (2004) 1104-1112
28. Lang C., et al. Transient expansion of synaptically connected dendritic spines upon induction of hippocampal long-term potentiation. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 16665-16670
29. Matsuzaki M., et al. Dendritic spine geometry is critical for AMPA receptor expression in hippocampal CA1 pyramidal neurons. Nat. Neurosci. 4 (2001) 1086-1092
30. Zhou Q., et al. Shrinkage of dendritic spines associated with long-term depression of hippocampal synapses. Neuron 44 (2004) 749-757
31. Trachtenberg J.T., et al. Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex. Nature 420 (2002) 788-794
32. Grutzendler J., et al. Long-term dendritic spine stability in the adult cortex. Nature 420 (2002) 812-816
33. Holtmaat A.J., et al. Transient and persistent dendritic spines in the neocortex in vivo. Neuron 45 (2005) 279-291
34. Zuo Y., et al. Development of long-term dendritic spine stability in diverse regions of cerebral cortex. Neuron 46 (2005) 181-189
35. Majewska A., et al. Remodeling of synaptic structure in sensory cortical areas in vivo. J. Neurosci. 26 (2006) 3021-3029
36. Engert F., and Bonhoeffer T. Dendritic spine changes associated with hippocampal long-term synaptic plasticity. Nature 399 (1999) 66-70
37. Maletic-Savatic M., et al. Rapid dendritic morphogenesis in CA1 hippocampal dendrites induced by synaptic activity. Science 283 (1999) 1923-1927
38. Nagerl U.V., et al. Bidirectional activity-dependent morphological plasticity in hippocampal neurons. Neuron 44 (2004) 759-767
39. Deng J., and Dunaevsky A. Dynamics of dendritic spines and their afferent terminals: spines are more motile than presynaptic boutons. Dev. Biol. 277 (2005) 366-377
40. Konur S., and Yuste R. Imaging the motility of dendritic protrusions and axon terminals: roles in axon sampling and synaptic competition. Mol. Cell. Neurosci. 27 (2004) 427-440
41. Majewska A., and 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. U. S. A. 100 (2003) 16024-16029
42. Tropea, D. et al. (2005) Influence of dark-rearing and subsequent light exposure on spine dynamics of primary visual cortical neurons in vivo. Program No. 714.9. In 2005 Abstract Viewer and Itinerary Planner, Society for Neuroscience Online (http://sfn.scholarone.com/)
43. Zuo Y., et al. Long-term sensory deprivation prevents dendritic spine loss in primary somatosensory cortex. Nature 436 (2005) 261-265
44. Wallace W., and Bear M.F. A morphological correlate of synaptic scaling in visual cortex. J. Neurosci. 24 (2004) 6928-6938
45. Trachtenberg J.T., and Stryker M.P. Rapid anatomical plasticity of horizontal connections in the developing visual cortex. J. Neurosci. 21 (2001) 3476-3482
46. Oray S., et al. Dendritic spine dynamics are regulated by monocular deprivation and extracellular matrix degradation. Neuron 44 (2004) 1021-1030
47. Antonini A., et al. Anatomical correlates of functional plasticity in mouse visual cortex. J. Neurosci. 19 (1999) 4388-4406
48. Silver M.A., and Stryker M.P. Distributions of synaptic vesicle proteins and GAD65 in deprived and nondeprived ocular dominance columns in layer IV of kitten primary visual cortex are unaffected by monocular deprivation. J. Comp. Neurol. 422 (2000) 652-664
49. Kind P.C., et al. Correlated binocular activity guides recovery from monocular deprivation. Nature 416 (2002) 430-433
50. Liao D.S., et al. Recovery of cortical binocularity and orientation selectivity after the critical period for ocular dominance plasticity. J. Neurophysiol. 92 (2004) 2113-2121
51. Sawtell N.B., et al. NMDA receptor-dependent ocular dominance plasticity in adult visual cortex. Neuron 38 (2003) 977-985
52. Hofer S., et al. Prior experience enhances plasticity in adult visual cortex. Nat. Neurosci. 9 (2006) 127-132
53. Kaas J., et al. Reorganization of retinotopic cortical maps in adult mammals after lesions of the retina. Science 248 (1990) 229-231
54. Gilbert C.D., and Wiesel T.N. Receptive field dynamics in adult primary visual cortex. Nature 356 (1992) 150-152
55. Darian-Smith C., and Gilbert C.D. Axonal sprouting accompanies functional reorganization in adult cat striate cortex. Nature 368 (1994) 737-740
56. Pettet M., and Gilbert C.D. Dynamic changes in receptive-field size in cat primary visual cortex. Proc. Natl. Acad. Sci. U. S. A. 89 (1992) 8366-8370
57. Turrigiano G., and Nelson S. Homeostatic plasticity in the developing nervous system. Nat. Rev. Neurosci. 5 (2004) 97-107
58. Hensch T. Critical period regulation. Annu. Rev. Neurosci. 27 (2004) 549-579
59. Marino J., et al. Invariant computations in local cortical networks with balanced excitation and inhibition. Nat. Neurosci. 8 (2005) 194-201
60. Konur S., and Yuste R. Developmental regulation of spine and filopodial motility in primary visual cortex: reduced effects of activity and sensory deprivation. J. Neurobiol. 59 (2004) 236-246
61. Daw N., et al. LTP and LTD vary with layer in rodent visual cortex. Vision Res. 44 (2004) 3377-3380
62. Hering H., and Sheng M. Dendritic spines: structure, dynamics and regulation. Nat. Rev. Neurosci. 2 (2001) 880-888
63. Dillon C., and Goda Y. The actin cytoskeleton: integrating form and function at the synapse. Annu. Rev. Neurosci. 28 (2005) 25-55
64. Matus A. Growth of dendritic spines: a continuing story. Curr. Opin. Neurobiol. 15 (2005) 67-72
65. Cho K., et al. An experimental test of the role of postsynaptic calcium levels in determining synaptic strength using perirhinal cortex of rat. J. Physiol. 532 (2001) 459-466
66. Heynen A.J., et al. Monocular mechanisms for loss of visual cortical responsiveness following brief monocular deprivation. Nat. Neurosci. 6 (2003) 854-862
67. Berardi N., et al. Molecular basis of plasticity in the visual cortex. Trends Neurosci. 26 (2003) 369-378
68. Kandel E.R. The molecular biology of memory storage: a dialogue between genes and synapses. Science 294 (2001) 1030-1038
69. Ossipow V., et al. Gene expression analysis of the critical period in the visual cortex. Mol. Cell. Neurosci. 27 (2004) 70-83
70. Taha S., et al. Autophosphorylation of αCaMKII is required for ocular dominance plasticity. Neuron 36 (2002) 483-491
71. Lisman J., et al. The molecular basis of CaMKII function in synaptic and behavioural memory. Nat. Rev. Neurosci. 3 (2002) 175-190
72. Colbran R.J., and Brown A.M. Calcium/calmodulin-dependent protein kinase II and synaptic plasticity. Curr. Opin. Neurobiol. 14 (2004) 318-327
73. Lamprecht R., and LeDoux J. Structural plasticity and memory. Nat. Rev. Neurosci. 5 (2004) 45-54
74. 2+ response element-binding protein function is essential for ocular dominance plasticity. J. Neurosci. 22 (2002) 2237-2245
75. Taha S., et al. Rapid ocular dominance plasticity requires cortical but not geniculate protein synthesis. Neuron 34 (2002) 425-436
76. Berardi N., et al. Extracellular matrix and visual cortical plasticity: freeing the synapse. Neuron 44 (2004) 905-908
77. Pizzorusso T., et al. Reactivation of ocular dominance plasticity in the adult visual cortex. Science 298 (2002) 1248-1251
78. Mataga N., et al. Permissive proteolytic activity for visual cortical plasticity. Proc. Natl. Acad. Sci. U. S. A. 99 (2002) 7717-7721
79. Mataga N., et al. Experience-dependent pruning of dendritic spines in visual cortex by tissue plasminogen activator. Neuron 44 (2004) 1031-1041
80. Sengpiel F., et al. Influence of experience on orientation maps in cat visual cortex. Nat. Neurosci. 2 (1999) 727-732
81. Sharma J., et al. Induction of visual orientation modules in auditory cortex. Nature 404 (2000) 841-847
82. von Melchner L., et al. Visual behaviour mediated by retinal projections directed to the auditory pathway. Nature 404 (2000) 871-876
83. Newton J.R., et al. Acceleration of visually cued conditioned fear through the auditory pathway. Nat. Neurosci. 7 (2004) 968-973
84. Somers D.C., et al. An emergent model of orientation selectivity in cat visual cortical simple cells. J. Neurosci. 15 (1995) 5448-5465
85. Dragoi V., et al. Dynamics of neuronal sensitivity in visual cortex and local feature discrimination. Nat. Neurosci. 5 (2002) 883-891
86. Ohki K., et al. Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex. Nature 433 (2005) 597-603
87. 2+ indicator proteins in transgenic mice under TET control. PLoS Biol. 2 (2004) e163
88. Grinvald A., and Hildesheim R. VSDI: a new era in functional imaging of cortical dynamics. Nat. Rev. Neurosci. 5 (2004) 874-885