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Volume 2011 (2011), Article ID 305621, 12 pages
Loss of Prestin Does Not Alter the Development of Auditory Cortical Dendritic Spines
1Program in Neuroscience, Harvard University, Cambridge, MA 02138, USA
2Department of Neurobiology and Anatomy, University of Rochester, Rochester, NY 14627, USA
3Department of Biomedical Engineering, University of Rochester, Rochester, NY 14627, USA
4Department of Brain & Cognitive Sciences, University of Rochester, Rochester, NY 14627, USA
5Center for Visual Science, University of Rochester, Rochester, NY 14627, USA
Received 2 January 2011; Accepted 1 March 2011
Academic Editor: M. B. Dutia
Copyright © 2011 L. J. Bogart 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.
- T. K. Hensch, “Critical period plasticity in local cortical circuits,” Nature Reviews Neuroscience, vol. 6, no. 11, pp. 877–888, 2005.
- K. Fox and R. O. L. Wong, “A comparison of experience-dependent plasticity in the visual and somatosensory systems,” Neuron, vol. 48, no. 3, pp. 465–477, 2005.
- D. H. Sanes and S. Bao, “Tuning up the developing auditory CNS,” Current Opinion in Neurobiology, vol. 19, no. 2, pp. 188–199, 2009.
- C. Vale and D. H. Sanes, “The effect of bilateral deafness on excitatory and inhibitory synaptic strength in the inferior colliculus,” European Journal of Neuroscience, vol. 16, no. 12, pp. 2394–2404, 2002.
- V. C. Kotak, S. Fujisawa, F. A. Lee, O. Karthikeyan, C. Aoki, and D. H. Sanes, “Hearing loss raises excitability in the auditory cortex,” Journal of Neuroscience, vol. 25, no. 15, pp. 3908–3918, 2005.
- H. Xu, V. C. Kotak, and D. H. Sanes, “Conductive hearing loss disrupts synaptic and spike adaptation in developing auditory cortex,” Journal of Neuroscience, vol. 27, no. 35, pp. 9417–9426, 2007.
- M. Fischer, S. Kaech, U. Wagner, H. Brinkhaus, and A. Matus, “Glutamate receptors regulate actin-based plasticity in dendritic spines,” Nature Neuroscience, vol. 3, no. 9, pp. 887–894, 2000.
- A. Dunaevsky, A. Tashiro, A. Majewska, C. Mason, and R. Yuste, “Developmental regulation of spine motility in the mammalian central nervous system,” Proceedings of the National Academy of Sciences of the United States of America, vol. 96, no. 23, pp. 13438–13443, 1999.
- E. Korkotian and M. Segal, “Regulation of dendritic spine motility in cultured hippocampal neurons,” Journal of Neuroscience, vol. 21, no. 16, pp. 6115–6124, 2001.
- E. N. Star, D. J. Kwiatkowski, and V. N. Murthy, “Rapid turnover of actin in dendritic spines and its regulation by activity,” Nature Neuroscience, vol. 5, no. 3, pp. 239–246, 2002.
- S. Oray, A. Majewska, and M. Sur, “Effects of synaptic activity on dendritic spine motility of developing cortical layer V pyramidal neurons,” Cerebral Cortex, vol. 16, no. 5, pp. 730–741, 2006.
- E. G. Gray, “Electron microscopy of synaptic contacts on dendrite spines of the cerebral cortex,” Nature, vol. 183, no. 4675, pp. 1592–1593, 1959.
- S. Ramón y Cajal, La Textura del Sistema Nerviosa del Hombre y Los Vertebrados, Moya, Madrid, Spain, 1904.
- M. Matsuzaki, G. C. R. Ellis-Davies, T. Nemoto, Y. Miyashita, M. Iino, and H. Kasai, “Dendritic spine geometry is critical for AMPA receptor expression in hippocampal CA1 pyramidal neurons,” Nature Neuroscience, vol. 4, no. 11, pp. 1086–1092, 2001.
- J. Noguchi, M. Matsuzaki, G. C. R. Ellis-Davies, and H. Kasai, “Spine-neck geometry determines NMDA receptor-dependent calcium signaling in dendrites,” Neuron, vol. 46, no. 4, pp. 609–622, 2005.
- C. Koch and A. Zador, “The function of dendritic spines: devices subserving biochemical rather than electrical compartmentalization,” Journal of Neuroscience, vol. 13, no. 2, pp. 413–422, 1993.
- A. Majewska, E. Brown, J. Ross, and R. Yuste, “Mechanisms of calcium decay kinetics in hippocampal spines: role of spine calcium pumps and calcium diffusion through the spine neck in biochemical compartmentalization,” Journal of Neuroscience, vol. 20, no. 5, pp. 1722–1734, 2000.
- A. Majewska, A. Tashiro, and R. Yuste, “Regulation of spine calcium dynamics by rapid spine motility,” Journal of Neuroscience, vol. 20, no. 22, pp. 8262–8268, 2000.
- P. Valverde, “Apical dendritic spines of the visual cortex and light deprivation in the mouse,” Experimental Brain Research, vol. 3, no. 4, pp. 337–352, 1967.
- M. Freire, “Effects of dark rearing on dendritic spines in layer IV of the mouse visual cortex. A quantitative electron microscopical study,” Journal of Anatomy, vol. 126, part 1, pp. 193–201, 1978.
- G. K. Bryan and A. H. Riesen, “Deprived somatosensory-motor experience in stumptailed monkey neocortex: dendritic spine density and dendritic branching of layer IIIB pyramidal cells,” Journal of Comparative Neurology, vol. 286, no. 2, pp. 208–217, 1989.
- A. Majewska and M. Sur, “Motility of dendritic spines in visual cortex in vivo: changes during the critical period and effects of visual deprivation,” Proceedings of the National Academy of Sciences of the United States of America, vol. 100, no. 26, pp. 16024–16029, 2003.
- W. Wallace and M. F. Bear, “A morphological correlate of synaptic scaling in visual cortex,” Journal of Neuroscience, vol. 24, no. 31, pp. 6928–6938, 2004.
- L. J. Lee, W. J. Chen, Y. W. Chuang, and Y. C. Wang, “Neonatal whisker trimming causes long-lasting changes in structure and function of the somatosensory system,” Experimental Neurology, vol. 219, no. 2, pp. 524–532, 2009.
- D. Tropea, A. K. Majewska, R. Garcia, and M. Sur, “Structural dynamics of synapses in vivo correlate with functional changes during experience-dependent plasticity in visual cortex,” Journal of Neuroscience, vol. 30, no. 33, pp. 11086–11095, 2010.
- M. C. Liberman, J. Gao, D. Z. Z. He, X. Wu, S. Jia, and J. Zuo, “Prestin is required for electromotility of the outer hair cell and for the cochlear amplifier,” Nature, vol. 419, no. 6904, pp. 300–304, 2002.
- M. C. Liberman, J. Zuo, and J. J. Guinan, “Otoacoustic emissions without somatic motility: can stereocilia mechanics drive the mammalian cochlea?” Journal of the Acoustical Society of America, vol. 116, no. 3, pp. 1649–1655, 2004.
- M. A. Cheatham, K. H. Huynh, J. Gao, J. Zuo, and P. Dallos, “Cochlear function in Prestin knockout mice,” Journal of Physiology, vol. 560, part 3, pp. 821–830, 2004.
- G. Feng, R. H. Mellor, M. Bernstein et al., “Imaging neuronal subsets in transgenic mice expressing multiple spectral variants of GFP,” Neuron, vol. 28, no. 1, pp. 41–51, 2000.
- K. B. J. Franklin and G. Paxinos, The Mouse Brain in Stereotaxic Coordinates, Academic Press, 2007.
- J. R. Ison, “The acoustic startle response in the mouse: reflex elicitation and reflex modification by preliminary stimuli,” in Handbook of Mouse Auditory Research: From Behavior to Molecular Biology, J. F. Willott, Ed., pp. 59–82, CRC Press, Boca Raton, Fla, USA, 2001.
- K. M. Harris and S. B. Kater, “Dendritic spines: cellular specializations imparting both stability and flexibility to synaptic function,” Annual Review of Neuroscience, vol. 17, pp. 341–371, 1994.
- C. Portera-Cailliau and J. T. Trachtenberg, “Dark-reared dendritic spines shed light on ocular dominance plasticity,” Cell Science Reviews, vol. 1, no. 3, pp. 1–10, 2005.
- Y. Zuo, G. Yang, E. Kwon, and W. B. Gan, “Long-term sensory deprivation prevents dendritic spine loss in primary somatosensory cortex,” Nature, vol. 436, no. 7048, pp. 261–265, 2005.
- D. Tropea, M. Sur, and A. K. Majewska, “Visual deprivation affects spine structural dynamics,” Communicative and Integrative Biology, vol. 4, no. 2, pp. 216–219, 2011.
- S. Oray, A. Majewska, and M. Sur, “Dendritic spine dynamics are regulated by monocular deprivation and extracellular matrix degradation,” Neuron, vol. 44, no. 6, pp. 1021–1030, 2004.
- A. J. G. D. Holtmaat, J. T. Trachtenberg, L. Wilbrecht et al., “Transient and persistent dendritic spines in the neocortex in vivo,” Neuron, vol. 45, no. 2, pp. 279–291, 2005.
- J. T. Trachtenberg, B. E. Chen, G. W. Knott et al., “Long-term in vivo imaging of experience-dependent synaptic plasticity in adult cortex,” Nature, vol. 420, no. 6917, pp. 788–794, 2002.
- A. Briner, M. De Roo, A. Dayer, D. Muller, J. Z. Kiss, and L. Vutskits, “Bilateral whisker trimming during early postnatal life impairs dendritic spine development in the mouse somatosensory barrel cortex,” Journal of Comparative Neurology, vol. 518, no. 10, pp. 1711–1723, 2010.
- G. G. Turrigiano, K. R. Leslie, N. S. Desai, L. C. Rutherford, and S. B. Nelson, “Activity-dependent scaling of quantal amplitude in neocortical neurons,” Nature, vol. 391, no. 6670, pp. 892–896, 1998.
- N. S. Desai, R. H. Cudmore, S. B. Nelson, and G. G. Turrigiano, “Critical periods for experience-dependent synaptic scaling in visual cortex,” Nature Neuroscience, vol. 5, no. 8, pp. 783–789, 2002.
- J. B. Fallon, D. R. F. Irvine, and R. K. Shepherd, “Cochlear implants and brain plasticity,” Hearing Research, vol. 238, no. 1-2, pp. 110–117, 2008.
- L. I. Zhang, S. Bao, and M. M. Merzenich, “Persistent and specific influences of early acoustic environments on primary auditory cortex,” Nature Neuroscience, vol. 4, no. 11, pp. 1123–1130, 2001.
- Y. K. Han, H. Köver, M. N. Insanally, J. H. Semerdjian, and S. Bao, “Early experience impairs perceptual discrimination,” Nature Neuroscience, vol. 10, no. 9, pp. 1191–1197, 2007.
- A. Kreczko, A. Goel, L. Song, and H. K. Lee, “Visual deprivation decreases somatic GAD65 puncta number on layer 2/3 pyramidal neurons in mouse visual cortex,” Neural Plasticity, vol. 2009, Article ID 415135, 7 pages, 2009.
- M. Bose, P. Muñoz-Llancao, S. Roychowdhury et al., “Effect of the environment on the dendritic morphology of the rat auditory cortex,” Synapse, vol. 64, no. 2, pp. 97–110, 2010.
- N. T. McMullen and E. M. Glaser, “Auditory cortical responses to neonatal deafening: pyramidal neuron spine loss without changes in growth or orientation,” Experimental Brain Research, vol. 72, no. 1, pp. 195–200, 1988.
- F. Valverde, “Structural changes in the area striata of the mouse after enucleation,” Experimental Brain Research, vol. 5, no. 4, pp. 274–292, 1968.
- A. M. M. Oswald and A. D. Reyes, “Maturation of intrinsic and synaptic properties of layer 2/3 pyramidal neurons in mouse auditory cortex,” Journal of Neurophysiology, vol. 99, no. 6, pp. 2998–3008, 2008.
- E. F. Chang and M. M. Merzenich, “Environmental noise retards auditory cortical development,” Science, vol. 300, no. 5618, pp. 498–502, 2003.
- F. Valverde, “Rate and extent of recovery from dark rearing in the visual cortex of the mouse,” Brain Research, vol. 33, no. 1, pp. 1–11, 1971.
- A. E. Takesian, V. C. Kotak, and D. H. Sanes, “Developmental hearing loss disrupts synaptic inhibition: implications for auditory processing,” Future Neurology, vol. 4, no. 3, pp. 331–349, 2009.
- J. Lu, Y. Cui, R. Cai, Y. Mao, J. Zhang, and X. Sun, “Early auditory deprivation alters expression of NMDA receptor subunit NR1 mRNA in the rat auditory cortex,” Journal of Neuroscience Research, vol. 86, no. 6, pp. 1290–1296, 2008.
- D. Nowicka and L. Kaczmarek, “Spatio-temporal pattern of N-methyl-D-aspartate receptor NR1 mRNA expression during postnatal development of visual structures of the rat brain,” Journal of Neuroscience Research, vol. 44, no. 5, pp. 471–477, 1996.
- E. M. Quinlan, B. D. Philpot, R. L. Huganir, and M. F. Bear, “Rapid, experience-dependent expression of synaptic NMDA receptors in visual cortex in vivo,” Nature Neuroscience, vol. 2, no. 4, pp. 352–357, 1999.
- T. Iwasato, A. Datwani, A. M. Wolf et al., “Cortex-restricted disruption of NMDAR1 impairs neuronal patterns in the barrel cortex,” Nature, vol. 406, no. 6797, pp. 726–731, 2000.
- L. J. Lee, T. Iwasato, S. Itohara, and R. S. Erzurumlu, “Exuberant thalamocortical axon arborization in cortex-specific NMDAR1 knockout mice,” Journal of Comparative Neurology, vol. 485, no. 4, pp. 280–292, 2005.
- V. C. Kotak, A. D. Breithaupt, and D. H. Sanes, “Developmental hearing loss eliminates long-term potentiation in the auditory cortex,” Proceedings of the National Academy of Sciences of the United States of America, vol. 104, no. 9, pp. 3550–3555, 2007.
- M. Matsuzaki, N. Honkura, G. C. R. Ellis-Davies, and H. Kasai, “Structural basis of long-term potentiation in single dendritic spines,” Nature, vol. 429, no. 6993, pp. 761–766, 2004.
- Q. Zhou, K. J. Homma, and MU. M. Poo, “Shrinkage of dendritic spines associated with long-term depression of hippocampal synapses,” Neuron, vol. 44, no. 5, pp. 749–757, 2004.
- C. D. Rittenhouse, B. A. Siegler, C. A. Voelker, H. Z. Shouval, M. A. Paradiso, and M. F. Bear, “Stimulus for rapid ocular dominance plasticity in visual cortex,” Journal of Neurophysiology, vol. 95, no. 5, pp. 2947–2950, 2006.
- A. Holtmaat, L. Wilbrecht, G. W. Knott, E. Welker, and K. Svoboda, “Experience-dependent and cell-type-specific spine growth in the neocortex,” Nature, vol. 441, no. 7096, pp. 979–983, 2006.
- R. Klinke, A. Kral, S. Heid, J. Tillein, and R. Hartmann, “Recruitment of the auditory cortex in congenitally deaf cats by long- term cochlear electrostimulation,” Science, vol. 285, no. 5434, pp. 1729–1733, 1999.
- A. Kral, R. Hartmann, J. Tillein, S. Heid, and R. Klinke, “Congenital auditory deprivation reduces synaptic activity within the auditory cortex in a layer-specific manner,” Cerebral Cortex, vol. 10, no. 7, pp. 714–726, 2000.
- N. Mataga, Y. Mizuguchi, and T. K. Hensch, “Experience-dependent pruning of dendritic spines in visual cortex by tissue plasminogen activator,” Neuron, vol. 44, no. 6, pp. 1031–1041, 2004.
- S. B. Hofer, T. D. Mrsic-Flogel, T. Bonhoeffer, and M. Hübener, “Experience leaves a lasting structural trace in cortical circuits,” Nature, vol. 457, no. 7227, pp. 313–317, 2009.
- D. Keith and A. El-Husseini, “Excitation control: balancing PSD-95 function at the synapse,” Frontiers in Molecular Neuroscience, vol. 1, article 4, 2008.
- Y. Lee, D. E. López, E. G. Meloni, and M. Davis, “A primary acoustic startle pathway: obligatory role of cochlear root neurons and the nucleus reticularis pontis caudalis,” Journal of Neuroscience, vol. 16, no. 11, pp. 3775–3789, 1996.
- J. R. Ison, P. D. Allen, and W. E. O'Neill, “Age-related hearing loss in C57BL/6J mice has both frequency-specific and non-frequency-specific components that produce a hyperacusis-like exaggeration of the acoustic startle reflex,” Journal of the Association for Research in Otolaryngology, vol. 8, no. 4, pp. 539–550, 2007.