Homeostatic Regulation of Eye-Specific Responses in Visual Cortex during Ocular Dominance Plasticity

Neuron

Volumn 54, Issue 6, 2007, Pages 961-972

  Mrsic Flogel, Thomas D ^a   Hofer, Sonja B ^a   Ohki, Kenichi ^b   Reid, R Clay ^b   Bonhoeffer, Tobias ^a   Hübener, Mark ^a  

^a MAX PLANCK INSTITUTE OF NEUROBIOLOGY   (Germany)

^b HARVARD MEDICAL SCHOOL   (United States)

Author keywords

MOLNEURO; SYSNEURO

Indexed keywords

CALCIUM;

ACCOMMODATION; ANIMAL CELL; ANIMAL EXPERIMENT; ARTICLE; CONTROLLED STUDY; EYE DOMINANCE; HOMEOSTASIS; MONOCULAR DEPRIVATION; NERVE CELL PLASTICITY; NONHUMAN; PRIORITY JOURNAL; VISUAL CORTEX;

ACTION POTENTIALS; ANIMALS; ANIMALS, NEWBORN; BRAIN MAPPING; CALCIUM; DOMINANCE, OCULAR; EYE; EYELIDS; MICE; MICE, INBRED C57BL; NEURONAL PLASTICITY; NEURONS; PHOTIC STIMULATION; SENSORY DEPRIVATION; TIME FACTORS; VISION, BINOCULAR; VISION, MONOCULAR; VISUAL CORTEX; VISUAL PATHWAYS;

EID: 34250205193     PISSN: 08966273     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.neuron.2007.05.028     Document Type: Article

References (48)

1. Abraham W.C., and Bear M.F. Metaplasticity: the plasticity of synaptic plasticity. Trends Neurosci. 19 (1996) 126-130
2. Antonini A., Fagiolini M., and Stryker M.P. Anatomical correlates of functional plasticity in mouse visual cortex. J. Neurosci. 19 (1999) 4388-4406
3. Bear M.F. Bidirectional synaptic plasticity: from theory to reality. Philos. Trans. R. Soc. Lond. B Biol. Sci. 358 (2003) 649-655
4. Bienenstock E.L., Cooper L.N., and Munro P.W. Theory for the development of neuron selectivity: orientation specificity and binocular interaction in visual cortex. J. Neurosci. 2 (1982) 32-48
5. Blais B.S., Shouval H.Z., and Cooper L.N. The role of presynaptic activity in monocular deprivation: comparison of homosynaptic and heterosynaptic mechanisms. Proc. Natl. Acad. Sci. USA 96 (1999) 1083-1087
6. Burrone J., and Murthy V.N. Synaptic gain control and homeostasis. Curr. Opin. Neurobiol. 13 (2003) 560-567
7. Chandrasekaran A.R., Shah R.D., and Crair M.C. Developmental homeostasis of mouse retinocollicular synapses. J. Neurosci. 27 (2007) 1746-1755
8. Clothiaux E.E., Bear M.F., and Cooper L.N. Synaptic plasticity in visual cortex: comparison of theory with experiment. J. Neurophysiol. 66 (1991) 1785-1804
9. Davis G.W. Homeostatic control of neural activity: from phenomenology to molecular design. Annu. Rev. Neurosci. 29 (2006) 307-323
10. Desai N.S. Homeostatic plasticity in the CNS: synaptic and intrinsic forms. J. Physiol. (Paris) 97 (2003) 391-402
11. Desai N.S., Cudmore R.H., Nelson S.B., and Turrigiano G.G. Critical periods for experience-dependent synaptic scaling in visual cortex. Nat. Neurosci. 5 (2002) 783-789
12. Dräger U.C. Autoradiography of tritiated proline and fucose transported transneuronally from the eye to the visual cortex in pigmented and albino mice. Brain Res. 82 (1974) 284-292
13. Dräger U.C. Receptive fields of single cells and topography in mouse visual cortex. J. Comp. Neurol. 160 (1975) 269-290
14. Fagiolini M., Fritschy J.M., Low K., Mohler H., Rudolph U., and Hensch T.K. Specific GABAA circuits for visual cortical plasticity. Science 303 (2004) 1681-1683
15. Frenkel M.Y., and Bear M.F. How monocular deprivation shifts ocular dominance in visual cortex of young mice. Neuron 44 (2004) 917-923
16. Frenkel M.Y., Sawtell N.B., Diogo A.C., Yoon B., Neve R.L., and Bear M.F. Instructive effect of visual experience in mouse visual cortex. Neuron 51 (2006) 339-349
17. Giannikopoulos D.V., and Eysel U.T. Dynamics and specificity of cortical map reorganization after retinal lesions. Proc. Natl. Acad. Sci. USA 103 (2006) 10805-10810
18. Gordon J.A., and Stryker M.P. Experience-dependent plasticity of binocular responses in the primary visual cortex of the mouse. J. Neurosci. 16 (1996) 3274-3286
19. Guillery R.W. Binocular competition in the control of geniculate cell growth. J. Comp. Neurol. 144 (1972) 117-129
20. Hensch T.K. Critical period plasticity in local cortical circuits. Nat. Rev. Neurosci. 6 (2005) 877-888
21. Heynen A.J., Yoon B.J., Liu C.H., Chung H.J., Huganir R.L., and Bear M.F. Molecular mechanism for loss of visual cortical responsiveness following brief monocular deprivation. Nat. Neurosci. 6 (2003) 854-862
22. Hofer S.B., Mrsic-Flogel T.D., Bonhoeffer T., and Hübener M. Lifelong learning: ocular dominance plasticity in mouse visual cortex. Curr. Opin. Neurobiol. 16 (2006) 451-459
23. Hofer S.B., Mrsic-Flogel T.D., Bonhoeffer T., and Hübener M. Prior experience enhances plasticity in adult visual cortex. Nat. Neurosci. 9 (2006) 127-132
24. Holtmaat A.J., Trachtenberg J.T., Wilbrecht L., Shepherd G.M., Zhang X., Knott G.W., and Svoboda K. Transient and persistent dendritic spines in the neocortex in vivo. Neuron 45 (2005) 279-291
25. Kerr J.N., Greenberg D., and Helmchen F. Imaging input and output of neocortical networks in vivo. Proc. Natl. Acad. Sci. USA 102 (2005) 14063-14068
26. Kirkwood A., Rioult M.C., and Bear M.F. Experience-dependent modification of synaptic plasticity in visual cortex. Nature 381 (1996) 526-528
27. Kotak V.C., Fujisawa S., Lee F.A., Karthikeyan O., Aoki C., and Sanes D.H. Hearing loss raises excitability in the auditory cortex. J. Neurosci. 25 (2005) 3908-3918
28. Maffei A., Nelson S.B., and Turrigiano G.G. Selective reconfiguration of layer 4 visual cortical circuitry by visual deprivation. Nat. Neurosci. 7 (2004) 1353-1359
29. Maffei A., Nataraj K., Nelson S.B., and Turrigiano G.G. Potentiation of cortical inhibition by visual deprivation. Nature 443 (2006) 81-84
30. Mao B.Q., Hamzei-Sichani F., Aronov D., Froemke R.C., and Yuste R. Dynamics of spontaneous activity in neocortical slices. Neuron 32 (2001) 883-898
31. Marder E., and Goaillard J.M. Variability, compensation and homeostasis in neuron and network function. Nat. Rev. Neurosci. 7 (2006) 563-574
32. Mataga N., Mizuguchi Y., and Hensch T.K. Experience-dependent pruning of dendritic spines in visual cortex by tissue plasminogen activator. Neuron 44 (2004) 1031-1041
33. Metin C., Godement P., and Imbert M. The primary visual cortex in the mouse: receptive field properties and functional organization. Exp. Brain Res. 69 (1988) 594-612
34. Miller K.D. Synaptic economics: competition and cooperation in synaptic plasticity. Neuron 17 (1996) 371-374
35. Ohki K., Chung S., Ch'ng Y.H., Kara P., and Reid R.C. Functional imaging with cellular resolution reveals precise micro-architecture in visual cortex. Nature 433 (2005) 597-603
36. Philpot B.D., Cho K.K., and Bear M.F. Obligatory role of NR2A for metaplasticity in visual cortex. Neuron 53 (2007) 495-502
37. Regehr W.G., and Tank D.W. Selective fura-2 loading of presynaptic terminals and nerve cell processes by local perfusion in mammalian brain slice. J. Neurosci. Methods 37 (1991) 111-119
38. Rittenhouse C.D., Shouval H.Z., Paradiso M.A., and Bear M.F. Monocular deprivation induces homosynaptic long-term depression in visual cortex. Nature 397 (1999) 347-350
39. Sawtell N.B., Frenkel M.Y., Philpot B.D., Nakazawa K., Tonegawa S., and Bear M.F. NMDA receptor-dependent ocular dominance plasticity in adult visual cortex. Neuron 38 (2003) 977-985
40. Schuett S., Bonhoeffer T., and Hübener M. Mapping retinotopic structure in mouse visual cortex with optical imaging. J. Neurosci. 22 (2002) 6549-6559
41. Smetters D., Majewska A., and Yuste R. Detecting action potentials in neuronal populations with calcium imaging. Methods 18 (1999) 215-221
42. Stellwagen D., and Malenka R.C. Synaptic scaling mediated by glial TNF-alpha. Nature 440 (2006) 1054-1059
43. Stosiek C., Garaschuk O., Holthoff K., and Konnerth A. In vivo two-photon calcium imaging of neuronal networks. Proc. Natl. Acad. Sci. USA 100 (2003) 7319-7324
44. Tagawa Y., Kanold P.O., Majdan M., and Shatz C.J. Multiple periods of functional ocular dominance plasticity in mouse visual cortex. Nat. Neurosci. 8 (2005) 380-388
45. Turrigiano G.G., and Nelson S.B. Homeostatic plasticity in the developing nervous system. Nat. Rev. Neurosci. 5 (2004) 97-107
46. Wiesel T.N., and Hubel D.H. Single cell responses in striate cortex of kittens deprived of vision in one eye. J. Neurophysiol. 26 (1963) 1003-1017
47. Yaksi E., and Friedrich R.W. Reconstruction of firing rate changes across neuronal populations by temporally deconvolved Ca2+ imaging. Nat. Methods 3 (2006) 377-383
48. Yang Y., Fischer Q.S., Zhang Y., Baumgartel K., Mansuy I.M., and Daw N.W. Reversible blockade of experience-dependent plasticity by calcineurin in mouse visual cortex. Nat. Neurosci. 8 (2005) 791-796