Cortical reorganization consistent with spike timing-but not correlation-dependent plasticity

Nature Neuroscience

Volumn 10, Issue 7, 2007, Pages 887-895

  Young, Joshua M ^a,b,c   Waleszczyk, Wioletta J ^c,d   Wang, Chun ^c   Calford, Michael B ^e   Dreher, Bogdan ^c   Obermayer, Klaus ^a,b  

^a TECHNISCHE UNIVERSITÄT BERLIN   (Germany)

^b HUMBOLDT UNIVERSITY   (Germany)

^c UNIVERSITY OF SYDNEY   (Australia)

^d NENCKI INSTITUTE OF EXPERIMENTAL BIOLOGY   (Poland)

^e UNIVERSITY OF NEWCASTLE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL EXPERIMENT; ARTICLE; BRAIN CORTEX; CORRELATION ANALYSIS; MATHEMATICAL COMPUTING; NERVE CELL; NERVE CELL PLASTICITY; NONHUMAN; POSTSYNAPTIC POTENTIAL; PRESYNAPTIC POTENTIAL; PRIORITY JOURNAL; SPIKE WAVE; VISUAL CORTEX;

ACTION POTENTIALS; ALGORITHMS; ANIMALS; CATS; ELECTROPHYSIOLOGY; EXCITATORY POSTSYNAPTIC POTENTIALS; FUNCTIONAL LATERALITY; HOMEOSTASIS; MODELS, NEUROLOGICAL; NEURAL NETWORKS (COMPUTER); NEURAL PATHWAYS; NEURONAL PLASTICITY; VISION, MONOCULAR; VISUAL CORTEX; VISUAL FIELDS;

EID: 34347346016     PISSN: 10976256     EISSN: None     Source Type: Journal    
DOI: 10.1038/nn1913     Document Type: Article

References (50)

1. Hubel, D.H. & Wiesel, T.N. Binocular interaction in striate cortex of kittens reared with artificial squint. J. Neurophysiol. 28, 1041-1059 (1965).
2. Katz, L.C. & Shatz, C.J. Synaptic activity and the construction of cortical circuits. Science 274, 1133-1138 (1996).
3. Hebb, D.O. The Organization of Behaviour (John Wiley & Sons, New York, 1949).
4. Stent, G.S. A physiological mechanism for Hebb's postulate of learning. Proc. Natl. Acad. Sci. USA 70, 997-1001 (1973).
5. Malenka, R.C. & Nicoll, R.A. NMDA receptor-dependent synaptic plasticity: multiple forms and mechanisms. Trends Neurosci. 16, 521-527 (1993).
6. Levy, W.B. & Steward, O. Temporal contiguity requirements for long-term associative potentiation/depression in the hippocampus. Neuroscience 8, 791-797 (1983).
7. Markram, H., Lubke, J., Frotscher, M. & Sakmann, B. Regulation of synaptic efficacy by coincidence of postsynaptic APs and EPSPs. Science 275, 213-215 (1997).
8. Song, S., Miller, K.D. & Abbott, L.F. Competitive Hebbian learning through spike-timing - dependent synaptic plasticity. Nat. Neurosci. 3, 919-926 (2000).
9. Sjöström, P.J., Turrigiano, G.G. & Nelson, S.B. Rate, timing, and cooperativity jointly determine cortical synaptic plasticity. Neuron 32, 1149-1164 (2001).
10. Froemke, R.C. & Dan, Y. Spike-timing-dependent synaptic modification induced by natural spike trains. Nature 416, 433-438 (2002).
11. Dan, Y. & Poo, M.-M. Spike timing-dependent plasticity of neural pircuits. Neuron 44, 23-30 (2004).
12. Pearson, J.C., Finkel, L.H. & Edelman, G.M. Plasticity in the organization of adult cerebral cortical maps: a computer simulation based on neuronal group selection. J. Neurosci. 7, 4209-4223 (1987).
13. Obermayer, K., Ritter, H. & Schulten, K. A principle for the formation of the spatial structure of cortical feature maps. Proc. Natl. Acad. Sci. USA 87, 8345-8349 (1990).
14. Hirsch, J.A. & Gilbert, C.D. Long-term changes in synaptic strength along specific intrinsic pathways in the cat visual cortex. J. Physiol. (Lond.) 461, 247-262 (1993).
15. Xing, J. & Gerstein, G.L. Networks with lateral connectivity. 3. Plasticity and reorganization of somatosensory cortex. J. Neurophysiol. 75, 217-232 (1996).
16. Miikkulainen, R., Bednar, J.A., Choe, Y. & Sirosh, J. Self-organization, plasticity and low-level visual phenomena in a laterally connected map model of the primary visual cortex. in Psychology of Learning and Motivation: Perceptual Learning (eds. Goldstone, R.L., Schyns, P.G. & Medin, D.L.) 257-308 (Academic Press, San Diego, 1997).
17. Feldman, D.E. Timing-based LTP and LTD at vertical inputs to layer II/III pyramidal cells in rat barrel cortex. Neuron 27, 45-56 (2000).
18. Song, S. & Abbott, L.F. Cortical development and remapping through spike timing-dependent plasticity. Neuron 32, 339-350 (2001).
19. Fu, Y.X. et al. Temporal specificity in the cortical plasticity of visual space representation. Science 296, 1999-2003 (2002).
20. Eyding, D., Schweigart, G. & Eysel, U.T. Spatio-temporal plasticity of cortical receptive fields in response to repetitive visual stimulation in the adult cat. Neuroscience 112, 195-215 (2002).
21. Celikel, T., Szostak, V.A. & Feldman, D.E. Modulation of spike timing by sensory deprivation during induction of cortical map plasticity. Nat. Neurosci. 7, 534-541 (2004).
22. Meliza, C.D. & Dan, Y. Receptive-field modification in rat visual cortex induced by paired visual stimulation and single-cell spiking. Neuron 49, 183-189 (2006).
23. Pettigrew, J.D. The effect of visual experience on the development of stimulus specificity by kitten cortical neurones. J. Physiol. (Lond.) 237, 49-74 (1974).
24. Giannikopoulos, D.V. & Eysel, U.T. Dynamics and specificity of cortical map reorganization after retinal lesions. Proc. Natl. Acad. Sci. USA 103, 10805-10810 (2006).
25. Olson, C.R. & Freeman, R.D. Profile of the sensitive period for monocular deprivation in kittens. Exp. Brain Res. 39, 17-21 (1980).
26. Kaas, J.H. et al. Reorganization of retinotopic cortical maps in adult mammals after lesions of the retina. Science 248, 229-231 (1990).
27. Chino, Y. et al. Recovery of binocular responses by cortical neurons after early monocular lesions. Nat. Neurosci. 4, 689-690 (2001).
28. Waleszczyk, W.J. et al. Laminar differences in plasticity in cat area 17 following retinal lesions in adolescence or adulthood. Eur. J. Neurosci. 17, 2351-2368 (2003).
29. Fitzgibbon, T., Funke, K. & Eysel, U.T. Anatomical correlations between soma size, axon diameter and intraretinal length for the α ganglion cells of the cat retina. Vis. Neurosci. 6, 159-174 (1991).
30. Calford, M.B., Schmid, L.M. & Rosa, M.G.P. Monocular focal retinal lesions induce short-term topographic plasticity in adult cat visual cortex. Proc. Biol. Soc. 266, 499-507 (1999).
31. Calford, M.B. et al. Plasticity in adult cat visual cortex (area 17) following circumscribed monocular lesions of all retinal layers. J. Physiol. (Lond.) 524, 587-602 (2000).
32. Gilbert, C.D. & Wiesel, T.N. Receptive field dynamics in adult primary visual cortex. Nature 356, 150-152 (1992).
33. Darian-Smith, C. & Gilbert, C.D. Topographic reorganization in the striate cortex of the adult cat and monkey is cortically mediated. J. Neurosci. 15, 1631-1647 (1995).
34. Calford, M.B., Wright, L.L., Metha, A.B. & Taglianetti, V. Topographic plasticity in primary visual cortex is mediated by local corticocortical connections. J. Neurosci. 23, 6434-6442 (2003).
35. Young, J.M., Waleszczyk, W.J., Burke, W., Calford, M.B. & Dreher, B. Topographic reorganization in area 18 of adult cats following circumscribed monocular retinal lesions in adolescence. J. Physiol. (Lond.) 541, 601-612 (2002).
36. Tusa, R.J., Palmer, L.A. & Rosenquist, A.C. The retinotopic organization of area 17 (striate cortex) in the cat. J. Comp. Neurol. 177, 213-235 (1978).
37. Tanifuji, M., Sugiyama, T. & Murase, K. Horizontal propagation of excitation in rat visual cortical slices revealed by optical imaging. Science 266, 1057-1059 (1994).
38. Jancke, D., Chavane, F., Naaman, S. & Grinvald, A. Imaging cortical correlates of illusion in early visual cortex. Nature 428, 423-426 (2004).
39. Chino, Y.M., Kaas, J.H., Smith, E.L., III, Langston, A.L. & Cheng, H. Rapid reorganization of cortical maps in adult cats following restricted deafferentation in retina. Vision Res. 32, 789-796 (1992).
40. Turrigiano, G.G., Leslie, K.R., Desai, N.S., Rutherford, L.C. & Nelson, S.B. Activity-dependent scaling of quantal amplitude in neocortical neurons. Nature 391, 892-896 (1998).
41. Desai, N.S., Cudmore, R.H., Nelson, S.B. & Turrigiano, G.G. Critical periods for experience-dependent synaptic scaling in visual cortex. Nat. Neurosci. 5, 783-789 (2002).
42. Rutherford, L.C., Nelson, S.B. & Turrigiano, G.G. BDNF has opposite effects on the quantal amplitude of pyramidal neuron and interneuron excitatory synapses. Neuron 21, 521-530 (1998).
43. Arckens, L. et al. Cooperative changes in GABA, glutamate and activity levels: the missing link in cortical plasticity. Eur. J. Neurosci. 12, 4222-4232 (2000).
44. Darian-Smith, C. & Gilbert, C.D. Axonal sprouting accompanies functional reorganization in adult cat striate cortex. Nature 368, 737-740 (1994).
45. Trachtenberg, J.T. & Stryker, M.P. Rapid anatomical plasticity of horizontal connections in the developing visual cortex. J. Neurosci. 21, 3476-3482 (2001).
46. Anderson, J.S., Carandini, M. & Ferster, D. Orientation tuning of input conductance, excitation and inhibition in cat primary visual cortex. J. Neurophysiol. 84, 909-926 (2000).
47. Yoshimura, Y. & Callaway, E.M. Fine-scale specificity of cortical networks depends on inhibitory cell type and connectivity. Nat. Neurosci. 8, 1552-1559 (2005).
48. Bringuier, V., Chavane, F., Glaeser, L. & Frégnac, Y. Horizontal propagation of visual activity in the synaptic integration field of area 17 neurons. Science 283, 695-699 (1999).
49. Hirsch, J.A. & Gilbert, C.D. Synaptic physiology of horizontal connections in the cat's visual cortex. J. Neurosci. 11, 1800-1809 (1991).
50. Colman, H., Nabekura, J. & Lichtman, J.W. Alterations in synaptic strength preceding axon withdrawal. Science 275, 356-361 (1997).