- About this Journal ·
- Abstracting and Indexing ·
- Advance Access ·
- Aims and Scope ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
Volume 2013 (2013), Article ID 605079, 8 pages
Gene Expression Patterns Underlying the Reinstatement of Plasticity in the Adult Visual System
1Neuroscience Centre, University of Helsinki, 00790 Helsinki, Finland
2SARS Institute, University of Bergen, 5020 Bergen, Norway
3Finnish Institute of Occupational Health, 00250 Helsinki, Finland
4Institute of Biotechnology, University of Helsinki, 00790 Helsinki, Finland
5Centre for Nanotechnology Innovation, Italian Institute of Technology, 56127 Pisa, Italy
6Centre for Neuroscience and Cognitive Systems, Italian Institute of Technology, 38068 Rovereto, Italy
7Neuroscience Institute, CNR, 56100 Pisa, Italy
Received 1 May 2013; Accepted 10 June 2013
Academic Editor: Alessandro Sale
Copyright © 2013 Ettore Tiraboschi et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
- L. C. Katz and C. J. Shatz, “Synaptic activity and the construction of cortical circuits,” Science, vol. 274, no. 5290, pp. 1133–1138, 1996.
- N. Berardi, T. Pizzorusso, and L. Maffei, “Critical periods during sensory development,” Current Opinion in Neurobiology, vol. 10, no. 1, pp. 138–145, 2000.
- V. B. Mountcastle, “The columnar organization of the neocortex,” Brain, vol. 120, part 4, pp. 701–722, 1997.
- D. Tropea, A. van Wart, and M. Sur, “Molecular mechanisms of experience-dependent plasticity in visual cortex,” Philosophical Transactions of the Royal Society B, vol. 364, no. 1515, pp. 341–355, 2009.
- D. H. Hubel and T. N. Wiesel, “The period of susceptibility to the physiological effects of unilateral eye closure in kittens,” Journal of Physiology, vol. 206, no. 2, pp. 419–436, 1970.
- T. N. Wiesel and D. H. Hubel, “Single-cell responses in striate cortex of kittens deprived of vision in one eye,” Journal of Neurophysiology, vol. 26, pp. 1003–1017, 1963.
- T. K. Hensch, “Critical period plasticity in local cortical circuits,” Nature Reviews Neuroscience, vol. 6, no. 11, pp. 877–888, 2005.
- J. F. Maya-Vetencourt, A. Sale, A. Viegi et al., “The antidepressant fluoxetine restores plasticity in the adult visual cortex,” Science, vol. 320, no. 5874, pp. 385–388, 2008.
- N. N. Karpova, A. Pickenhagen, J. Lindholm et al., “Fear erasure in mice requires synergy between antidepressant drugs and extinction training,” Science, vol. 334, no. 6063, pp. 1731–1734, 2011.
- C. Orlando, J. Ster, U. Gerber, J. W. Fawcett, and O. Raineteau, “Perisynaptic chondroitin sulfate proteoglycans restrict structural plasticity in an integrin-dependent manner,” The Journal of Neuroscience, vol. 32, Article ID 18017a, pp. 18009–18017, 2012.
- T. Pizzorusso, P. Medini, N. Berardi, S. Chierzi, J. W. Fawcett, and L. Maffei, “Reactivation of ocular dominance plasticity in the adult visual cortex,” Science, vol. 298, no. 5596, pp. 1248–1251, 2002.
- L. Baroncelli, A. Sale, A. Viegi et al., “Experience-dependent reactivation of ocular dominance plasticity in the adult visual cortex,” Experimental Neurology, vol. 226, no. 1, pp. 100–109, 2010.
- A. Sale, J. F. Maya-Vetencourt, P. Medini et al., “Environmental enrichment in adulthood promotes amblyopia recovery through a reduction of intracortical inhibition,” Nature Neuroscience, vol. 10, no. 6, pp. 679–681, 2007.
- A. Sale, N. Berardi, and L. Maffei, “Enrich the environment to empower the brain,” Trends in Neurosciences, vol. 32, no. 4, pp. 233–239, 2009.
- M. Scali, L. Baroncelli, M. C. Cenni, A. Sale, and L. Maffei, “A rich environmental experience reactivates visual cortex plasticity in aged rats,” Experimental Gerontology, vol. 47, no. 4, pp. 337–341, 2012.
- M. Spolidoro, L. Baroncelli, E. Putignano, J. F. Maya-Vetencourt, A. Viegi, and L. Maffei, “Food restriction enhances visual cortex plasticity in adulthood,” Nature Communications, vol. 2, no. 1, article 320, 2011.
- J. F. Maya-Vetencourt, E. Tiraboschi, D. Greco et al., “Experience-dependent expression of NPAS4 regulates plasticity in adult visual cortex,” The Journal of Physiology, vol. 590, pp. 4777–4787, 2012.
- S. Miyata, Y. Komatsu, Y. Yoshimura, C. Taya, and H. Kitagawa, “Persistent cortical plasticity by upregulation of chondroitin 6-sulfation,” Nature Neuroscience, vol. 15, no. 3, pp. 414–422, 2012.
- D. Bavelier, D. M. Levi, R. W. Li, Y. Dan, and T. K. Hensch, “Removing brakes on adult brain plasticity: from molecular to behavioral interventions,” The Journal of Neuroscience, vol. 30, no. 45, pp. 14964–14971, 2010.
- M. Beurdeley, J. Spatazza, H. H. C. Lee et al., “Otx2 binding to perineuronal nets persistently regulates plasticity in the mature visual cortex,” The Journal of Neuroscience, vol. 32, pp. 9429–9437, 2012.
- H. Morishita, J. M. Miwa, N. Heintz, and T. K. Hensch, “Lynx1, a cholinergic brake, limits plasticity in adult visual cortex,” Science, vol. 330, no. 6008, pp. 1238–1240, 2010.
- Z. J. Huang, A. Kirkwood, T. Pizzorusso et al., “BDNF regulates the maturation of inhibition and the critical period of plasticity in mouse visual cortex,” Cell, vol. 98, no. 6, pp. 739–755, 1999.
- D. G. Southwell, R. C. Froemke, A. Alvarez-Buylla, M. P. Stryker, and S. P. Gandhi, “Cortical plasticity induced by inhibitory neuron transplantation,” Science, vol. 327, no. 5969, pp. 1145–1148, 2010.
- G. Di Cristo, B. Chattopadhyaya, S. J. Kuhlman et al., “Activity-dependent PSA expression regulates inhibitory maturation and onset of critical period plasticity,” Nature Neuroscience, vol. 10, no. 12, pp. 1569–1577, 2007.
- T. A. Pham, S. Impey, D. R. Storm, and M. P. Stryker, “Cre-mediated gene transcription in neocortical neuronal plasticity during the developmental critical period,” Neuron, vol. 22, no. 1, pp. 63–72, 1999.
- E. Putignano, G. Lonetti, L. Cancedda et al., “Developmental downregulation of histone posttranslational modifications regulates visual cortical plasticity,” Neuron, vol. 53, no. 5, pp. 747–759, 2007.
- Y. Wang, Q. Gu, and M. S. Cynader, “Blockade of serotonin-2C receptors by mesulergine reduces ocular dominance plasticity in kitten visual cortex,” Experimental Brain Research, vol. 114, no. 2, pp. 321–328, 1997.
- Q. Gu and W. Singer, “Involvement of serotonin in developmental plasticity of kitten visual cortex,” The European Journal of Neuroscience, vol. 7, no. 6, pp. 1146–1153, 1995.
- J. F. Maya-Vetencourt, E. Tiraboschi, M. Spolidoro, E. Castrén, and L. Maffei, “Serotonin triggers a transient epigenetic mechanism that reinstates adult visual cortex plasticity in rats,” The European Journal of Neuroscience, vol. 33, no. 1, pp. 49–57, 2011.
- K. J. Livak and T. D. Schmittgen, “Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method,” Methods, vol. 25, no. 4, pp. 402–408, 2001.
- M. Fagiolini and T. K. Hensch, “Inhibitory threshold for critical-period activation in primary visual cortex,” Nature, vol. 404, no. 6774, pp. 183–186, 2000.
- T. K. Hensch, M. Fagiolini, N. Mataga, M. P. Stryker, S. Baekkeskov, and S. F. Kash, “Local GABA circuit control of experience-dependent plasticity in developing visual cortex,” Science, vol. 282, no. 5393, pp. 1504–1508, 1998.
- A. W. McGee, Y. Yang, Q. S. Fischer, N. W. Daw, and S. H. Strittmatter, “Neuroscience: experience-driven plasticity of visual cortex limited by myelin and nogo receptor,” Science, vol. 309, no. 5744, pp. 2222–2226, 2005.
- E. J. Weeber, U. Beffert, C. Jones et al., “Reelin and ApoE receptors cooperate to enhance hippocampal synaptic plasticity and learning,” The Journal of Biological Chemistry, vol. 277, no. 42, pp. 39944–39952, 2002.
- T. M. Reeves, M. L. Prins, J. Zhu, J. T. Povlishock, and L. L. Phillips, “Matrix metalloproteinase inhibition alters functional and structural correlates of deafferentation-induced sprouting in the dentate gyrus,” The Journal of Neuroscience, vol. 23, no. 32, pp. 10182–10189, 2003.
- J. Zuo, T. A. Ferguson, Y. J. Hernandez, W. G. Stetler-Stevenson, and D. Muir, “Neuronal matrix metalloproteinase-2 degrades and inactivates a neurite- inhibiting chondroitin sulfate proteoglycan,” The Journal of Neuroscience, vol. 18, no. 14, pp. 5203–5211, 1998.
- V. W. Yong, C. Power, P. Forsyth, and D. R. Edwards, “Metalloproteinases in biology and pathology of the nervous system,” Nature Reviews Neuroscience, vol. 2, no. 7, pp. 502–511, 2001.
- V. Nagy, O. Bozdagi, A. Matynia et al., “Matrix metalloproteinase-9 is required for hippocampal late-phase long-term potentiation and memory,” The Journal of Neuroscience, vol. 26, no. 7, pp. 1923–1934, 2006.
- S. E. Meighan, P. C. Meighan, P. Choudhury et al., “Effects of extracellular matrix-degrading proteases matrix metalloproteinases 3 and 9 on spatial learning and synaptic plasticity,” Journal of Neurochemistry, vol. 96, no. 5, pp. 1227–1241, 2006.
- J. F. Maya-Vetencourt and N. Origlia, “Visual cortex plasticity: a complex interplay of genetic and environmental influences,” Neural Plasticity, vol. 2012, Article ID 631965, 14 pages, 2012.
- J. Herz and Y. Chen, “Reelin, lipoprotein receptors and synaptic plasticity,” Nature Reviews Neuroscience, vol. 7, no. 11, pp. 850–859, 2006.
- G. D'Arcangelo, G. G. Miao, S.-C. Chen, H. D. Soares, J. I. Morgan, and T. Curran, “A protein related to extracellular matrix proteins deleted in the mouse mutant reeler,” Nature, vol. 374, no. 6524, pp. 719–723, 1995.
- S. H. Fatemi, “Reelin glycoprotein: structure, biology and roles in health and disease,” Molecular Psychiatry, vol. 10, no. 3, pp. 251–257, 2005.
- E. Soriano and J. A. del Río, “The cells of cajal-retzius: still a mystery one century after,” Neuron, vol. 46, no. 3, pp. 389–394, 2005.
- S. Hellwig, I. Hack, J. Kowalski et al., “Role for reelin in neurotransmitter release,” The Journal of Neuroscience, vol. 31, no. 7, pp. 2352–2360, 2011.
- T. Hajszan, N. J. MacLusky, and C. Leranth, “Short-term treatment with the antidepressant fluoxetine triggers pyramidal dendritic spine synapse formation in rat hippocampus,” The European Journal of Neuroscience, vol. 21, no. 5, pp. 1299–1303, 2005.
- R. Guirado, E. Varea, E. Castillo-Gómez et al., “Effects of chronic fluoxetine treatment on the rat somatosensory cortex: activation and induction of neuronal structural plasticity,” Neuroscience Letters, vol. 457, no. 1, pp. 12–15, 2009.
- S. H. Fatemi, T. J. Reutiman, and T. D. Folsom, “Chronic psychotropic drug treatment causes differential expression of Reelin signaling system in frontal cortex of rats,” Schizophrenia Research, vol. 111, no. 1–3, pp. 138–152, 2009.
- R. Guirado, D. Sanchez-Matarredona, E. Varea, C. Crespo, J. M. Blasco-Ibáñez, and J. Nacher, “Chronic fluoxetine treatment in middle-aged rats induces changes in the expression of plasticity-related molecules and in neurogenesis,” BMC Neuroscience, vol. 13, no. 1, article 5, 2012.
- J. L. Chen, W. C. Lin, J. W. Cha, P. T. So, Y. Kubota, and E. Nedivi, “Structural basis for the role of inhibition in facilitating adult brain plasticity,” Nature Neuroscience, vol. 14, no. 5, pp. 587–596, 2011.
- A. C. Flint, U. S. Maisch, J. H. Weishaupt, A. R. Kriegstein, and H. Monyer, “NR2A subunit expression shortens NMDA receptor synaptic currents in developing neocortex,” The Journal of Neuroscience, vol. 17, no. 7, pp. 2469–2476, 1997.
- G. Carmignoto and S. Vicini, “Activity-dependent decrease in NMDA receptor responses during development of the visual cortex,” Science, vol. 258, no. 5084, pp. 1007–1011, 1992.
- K. K. A. Cho, L. Khibnik, B. D. Philpot, and M. F. Bear, “The ratio of NR2A/B NMDA receptor subunits determines the qualities of ocular dominance plasticity in visual cortex,” Proceedings of the National Academy of Sciences of the United States of America, vol. 106, no. 13, pp. 5377–5382, 2009.
- A. W. Lyckman, S. Horng, C. A. Leamey et al., “Gene expression patterns in visual cortex during the critical period: synaptic stabilization and reversal by visual deprivation,” Proceedings of the National Academy of Sciences of the United States of America, vol. 105, no. 27, pp. 9409–9414, 2008.
- E. Castrén and T. Rantamäki, “The role of BDNF and its receptors in depression and antidepressant drug action: reactivation of developmental plasticity,” Developmental Neurobiology, vol. 70, no. 5, pp. 289–297, 2010.
- N. Tsankova, W. Renthal, A. Kumar, and E. J. Nestler, “Epigenetic regulation in psychiatric disorders,” Nature Reviews Neuroscience, vol. 8, no. 5, pp. 355–367, 2007.