Selective acquisition of AMPA receptors over postnatal development suggests a molecular basis for silent synapses (original) (raw)
References
Hollmann, M. & Heinemann, S. Cloned glutamate receptors. Annu. Rev. Neurosci.17, 31–108 (1994). ArticleCAS Google Scholar
Liao, D. & Malinow, R. Deficiency in induction but not expression of LTP in hippocampal slices from young rats. Learn. Mem.3, 138–149 ( 1996). ArticleCAS Google Scholar
Durand, G., Kovalchuk, Y. & Konnerth, A. Long–term potentiation and functional synapse induction in developing hippocampus. Nature381, 71–75 (1996). ArticleCAS Google Scholar
Hsia, A. Y., Malenka, R. C. & Nicoll, R. A. Development of excitatory circuitry in the hippocampus. J. Neurophysiol.79, 2013– 2024 (1998). ArticleCAS Google Scholar
Wu, G.–Y., Malinow, R. & Cline, H. T. Maturation of a central glutamatergic synapse. Science274, 972–976 ( 1996). ArticleCAS Google Scholar
Isaac, J. T., Crair, M. C., Nicoll, R. A. & Malenka, R. C. Silent synapses during development of thalamocortical inputs. Neuron18, 269–280 ( 1997). ArticleCAS Google Scholar
Liao, D., Hessler, N. A. & Malinow, R. Activation of postsynaptically silent synapses during pairing–induced LTP in CA1 region of hippocampal slice. Nature375, 400–404 ( 1995). ArticleCAS Google Scholar
Isaac, J. T., Nicoll, R. A. & Malenka, R. C. Evidence for silent synapses: implications for the expression of LTP. Neuron15, 427– 434 (1995). ArticleCAS Google Scholar
Mayer, M. L., Westbrook, G. L. & Guthrie, P. B. Voltage–dependent block by Mg2+ of NMDA responses in spinal cord neurons. Nature309 , 261–263 (1984). ArticleCAS Google Scholar
Rusakov, D. A. & Kullmann, D. M. Extrasynaptic glutamate diffusion in the hippocampus: ultrastructural constraints, uptake, and receptor activation. J. Neurosci.18, 3158–3170 (1998). ArticleCAS Google Scholar
Kullmann, D. M. & Asztely, F. Extrasynaptic glutamate spillover in the hippocampus: evidence and implications. Trends Neurosci.21, 8–14 (1998). ArticleCAS Google Scholar
Dong, H. et al. GRIP: a synaptic PDZ domain–containing protein that interacts with AMPA receptors. Nature386, 279– 284 (1997). ArticleCAS Google Scholar
Barria, A., Muller, D., Derkach, V., Griffith, L. C. & Soderling, T. R. Regulatory phosphorylation of AMPA–type glutamate receptors by CaM–KII during long–term potentiation. Science276, 2042–2045 ( 1997). ArticleCAS Google Scholar
Kharazia, V. N., Phend, K. D., Rustioni, A. & Weinberg, R. J. EM colocalization of AMPA and NMDA receptor subunits at synapses in rat cerebral cortex. Neurosci. Lett. 210, 37– 40 (1996). ArticleCAS Google Scholar
Desmond, N. L. & Weinberg, R. J. Enhanced expression of AMPA receptor protein at perforated axospinous synapses. Neuroreport9, 857–860 ( 1998). ArticleCAS Google Scholar
Wenthold, R. J., Petralia, R. S., Blahos, J. II & Niedzielski, A. S. Evidence for multiple AMPA receptor complexes in hippocampal CA1/CA2 neurons. J. Neurosci.16, 1982–1989 (1996). ArticleCAS Google Scholar
Bekkers, J. M., Richerson, G. B. & Stevens, C. F. Origin of variability in quantal size in cultured hippocampal neurons and hippocampal slices. Proc. Natl. Acad. Sci. USA87, 5359–5362 ( 1990). ArticleCAS Google Scholar
Shatz, C. J. Impulse activity and the patterning of connections during CNS development. Neuron5, 745–756 (1990). ArticleCAS Google Scholar
Fox, K. The critical period for long–term potentiation in primary sensory cortex. Neuron15, 485–488 (1995). ArticleCAS Google Scholar
Katz, L. C. & Shatz, C. J. Synaptic activity and the construction of cortical circuits. Science274, 1132– 1138 (1996). Article Google Scholar
Constantine–Paton, M. & Cline, H. T. LTP and activity–dependent synaptogenesis: the more alike they are, the more different they become. Curr. Opin. Neurobiol.8, 139–148 (1998). Article Google Scholar
Wang, Y.–X., Wenthold, R. J., Ottersen, O. P. & Petralia, R. S. Endbulb synapses in the anteroventral cochlear nucleus express a specific subset of AMPA–type glutamate receptor subunits. J. Neurosci.18, 1148–1160 ( 1998). ArticleCAS Google Scholar
Zhao, H.–M., Wenthold, R. J. & Petralia, R. S. Glutamate receptor targeting to synaptic populations on Purkinje cells is developmentally regulated. J. Neurosci. 18, 5517–5528 (1998). ArticleCAS Google Scholar
Matsubara, A., Laake, J. H., Davanger, S., Usami, S. & Ottersen, O. P. Organization of AMPA receptor subunits at a glutamate synapse: a quantitative immunogold analysis of hair cell synapses in the rat organ of Corti. J. Neurosci.16, 4457–4467 (1996). ArticleCAS Google Scholar
Wang, B.–L. & Larsson, L.–I. Simultaneous demonstration of multiple antigens by indirect immunofluorescence or immunogold staining. Novel light and electron microscopical double and triple staining method employing primary antibodies from the same species. Histochemistry83, 47–56 ( 1985). ArticleCAS Google Scholar
Wenthold, R. J., Yokotani, N., Doi, K. & Wada, K. Immunochemical characterization of the non–NMDA glutamate receptor using subunit–specific antibodies. Evidence for a hetero–oligomeric structure in rat brain. J. Biol. Chem.267, 501–507 (1992). CAS Google Scholar
Petralia, R. S. & Wenthold, R. J. Light and electron immunocytochemical localization of AMPA–selective glutamate receptors in the rat brain. J. Comp. Neurol.318, 329–354 (1992). ArticleCAS Google Scholar
Petralia, R. S., Yokotani, N. & Wenthold, R. J. Light and electron microscope distribution of the NMDA receptor subunit NMDAR1 in the rat nervous system using a selective anti–peptide antibody. J. Neurosci.14, 667– 696 (1994). ArticleCAS Google Scholar
Petralia, R. S., Wang, Y.–X. & Wenthold, R. J. The NMDA receptor subunits NR2A and NR2B show histological and ultrastructural localization patterns similar to those of NR1. J. Neurosci.14, 6102–6120 (1994). ArticleCAS Google Scholar
Petralia, R. S., Wang, Y.–X., Mayat, E. & Wenthold, R. J. Glutamate receptor subunit 2–selective antibody shows a differential distribution of calcium–impermeable AMPA receptors among populations of neurons. J. Comp. Neurol.385, 456– 476 (1997). ArticleCAS Google Scholar
Johnson, M. L. & Faunt, L. M. Parameter estimation by least–squares methods. Methods Enzymol.210 , 1–37 (1992). ArticleCAS Google Scholar
Straume, M. & Johnson, M. L. Monte Carlo method for determining complete confidence probability distributions of estimated model parameters. Methods Enzymol. 210, 117– 129 (1992). ArticleCAS Google Scholar