SEARCH

SEARCH BY CITATION

References

  • Allen N. J., Bennett M. L., Foo L. C., Wang G. X., Chakraborty C., Smith S. J. and Barres B. A. (2012) Astrocyte glypicans 4 and 6 promote formation of excitatory synapses via GluA1 AMPA receptors. Nature 486, 410414.
  • Aya-ay J., Mayer J., Eakin A. K., Muffly B. G., Anello M., Sandy J. D. and Gottschall P. E. (2005) The effect of hypoxic-ischemic brain injury in perinatal rats on the abundance and proteolysis of brevican and NG2. Exp. Neurol. 193, 149162.
  • Bandtlow C. E. and Zimmermann D. R. (2000) Proteoglycans in the developing brain: new conceptual insights for old proteins. Physiol. Rev. 80, 12671290.
  • Beyreuther K., Pollwein P., Multhaup G., Monning U., Konig G., Dyrks T., Schubert W. and Masters C. L. (1993) Regulation and expression of the Alzheimer's beta/A4 amyloid protein precursor in health, disease, and Down's syndrome. Ann. N. Y. Acad. Sci. 695, 91102.
  • Brakebusch C., Seidenbecher C. I., Asztely F. et al. (2002) Brevican-deficient mice display impaired hippocampal CA1 long-term potentiation but show no obvious deficits in learning and memory. Mol. Cell. Biol. 22, 74177427.
  • Butler C. D., Schnetz S. A., Yu E. Y., Davis J. B., Temple K., Silver J. and Malouf A. T. (2004) Keratan sulfate proteoglycan phosphacan regulates mossy fiber outgrowth and regeneration. J. Neurosci. 24, 462473.
  • Celio M. R., Spreafico R., De Biasi S. and Vitellaro-Zuccarello L. (1998) Perineuronal nets: past and present. Trends Neurosci. 21, 510515.
  • Conboy L. and Sandi C. (2010) Stress at learning facilitates memory formation by regulating AMPA receptor trafficking through a glucocorticoid action. Neuropsychopharmacology 35, 674685.
  • Daniels M. P. (2012) The role of agrin in synaptic development, plasticity and signaling in the central nervous system. Neurochem. Int. 61, 848853.
  • Emond M. R., Montgomery J. M., Huggins M. L., Hanson J. E., Mao L., Huganir R. L. and Madison D. V. (2010) AMPA receptor subunits define properties of state-dependent synaptic plasticity. J. Physiol. 588, 19291946.
  • Falsafi S. K., Ghafari M., Pollak A., Hoger H. and Lubec G. (2012) Hippocampal AMPA-type receptor complexes containing GluR3 and GluR4 are paralleling training in the Multiple T-Maze. Neurochem. Int. 60, 425430.
  • Ferreira A. (1999) Abnormal synapse formation in agrin-depleted hippocampal neurons. J. Cell Sci. 112, 47294738.
  • Frischknecht R., Heine M., Perrais D., Seidenbecher C. I., Choquet D. and Gundelfinger E. D. (2009) Brain extracellular matrix affects AMPA receptor lateral mobility and short-term synaptic plasticity. Nat. Neurosci. 12, 897904.
  • Ghafari M., Falsafi S. K., Hoeger H. and Lubec G. (2012a) Hippocampal levels of GluR1 and GluR2 complexes are modulated by training in the Multiple T-maze in C57BL/6J mice. Brain Struct. Funct. 217, 353362.
  • Ghafari M., Hoger H., Keihan Falsafi S., Russo-Schlaff N., Pollak A. and Lubec G. (2012b) Mass spectrometrical identification of hippocampal NMDA receptor subunits NR1, NR2A-D and five novel phosphorylation sites on NR2A and NR2B. J. Proteome Res. 11, 18911896.
  • Gogolla N., Caroni P., Luthi A. and Herry C. (2009) Perineuronal nets protect fear memories from erasure. Science 325, 12581261.
  • Hensch T. K. (2005) Critical period plasticity in local cortical circuits. Nat. Rev. Neurosci. 6, 877888.
  • Herndon M. E. and Lander A. D. (1990) A diverse set of developmentally regulated proteoglycans is expressed in the rat central nervous system. Neuron 4, 949961.
  • Krugers H. J. and Hoogenraad C. C. (2009) Hormonal regulation of AMPA receptor trafficking and memory formation. Front. Synaptic Neurosci. 1, 2.
  • Kurazono S., Okamoto M., Mori S. and Matsui H. (2001) Recombinant core protein fragment of phosphacan, a brain specific chondroitin sulfate proteoglycan, promote excitotoxic cell death of cultured rat hippocampal neurons. Neurosci. Lett. 304, 169172.
  • Lee A. M., Kanter B. R., Wang D., Lim J. P., Zou M. E., Qiu C., McMahon T., Dadgar J., Fischbach-Weiss S. C. and Messing R. O. (2013) Prkcz null mice show normal learning and memory. Nature 493, 416419.
  • Leonardo C. C., Eakin A. K., Ajmo J. M. and Gottschall P. E. (2008) Versican and brevican are expressed with distinct pathology in neonatal hypoxic-ischemic injury. J. Neurosci. Res. 86, 11061114.
  • Morawski M., Bruckner G., Jager C., Seeger G., Matthews R. T. and Arendt T. (2012) Involvement of perineuronal and perisynaptic extracellular matrix in Alzheimer's disease neuropathology. Brain Pathol. 22, 547561.
  • Nikonenko A., Schmidt S., Skibo G., Bruckner G. and Schachner M. (2003) Tenascin-R-deficient mice show structural alterations of symmetric perisomatic synapses in the CA1 region of the hippocampus. J. Comp. Neurol. 456, 338349.
  • Orlando C., Ster J., Gerber U., Fawcett J. W. and Raineteau O. (2012) Perisynaptic chondroitin sulfate proteoglycans restrict structural plasticity in an integrin-dependent manner. J. Neurosci. 32, 1800918017.
  • Pantazopoulos H., Woo T. U., Lim M. P., Lange N. and Berretta S. (2010) Extracellular matrix-glial abnormalities in the amygdala and entorhinal cortex of subjects diagnosed with schizophrenia. Arch. Gen. Psychiatry 67, 155166.
  • Reimers J. M., Milovanovic M. and Wolf M. E. (2011) Quantitative analysis of AMPA receptor subunit composition in addiction-related brain regions. Brain Res. 1367, 223233.
  • Rust M. B., Gurniak C. B., Renner M. et al. (2010) Learning, AMPA receptor mobility and synaptic plasticity depend on n-cofilin-mediated actin dynamics. EMBO J. 29, 18891902.
  • Saghatelyan A. K., Gorissen S., Albert M., Hertlein B., Schachner M. and Dityatev A. (2000) The extracellular matrix molecule tenascin-R and its HNK-1 carbohydrate modulate perisomatic inhibition and long-term potentiation in the CA1 region of the hippocampus. Eur. J. Neurosci. 12, 33313342.
  • Sase S., Khan D., Sialana F., Hoger H., Russo-Schlaff N. and Lubec G. (2012) Modafinil improves performance in the multiple T-Maze and modifies GluR1, GluR2, D2 and NR1 receptor complex levels in the C57BL/6J mouse. Amino Acids 43, 22852292.
  • Sase A., Dahanayaka S., Hoger H., Wu G. and Lubec G. (2013) Changes of hippocampal beta-alanine and citrulline levels are paralleling early and late phase of retrieval in the Morris Water Maze. Behav. Brain Res. 249, 104108.
  • Schwenk J., Harmel N., Brechet A. et al. (2012) High-resolution proteomics unravel architecture and molecular diversity of native AMPA receptor complexes. Neuron 74, 621633.
  • Senkov O., Tikhobrazova O. and Dityatev A. (2012) PSA-NCAM: synaptic functions mediated by its interactions with proteoglycans and glutamate receptors. Int. J. Biochem. Cell Biol. 44, 591595.
  • Shah A. and Lodge D. J. (2013) A loss of hippocampal perineuronal nets produces deficits in dopamine system function: relevance to the positive symptoms of schizophrenia. Transl. Psychiatry 3, e215.
  • Wan J., Csaszar E., Chen W. Q., Li K. and Lubec G. (2012) Proteins from Avastin® (bevacizumab) show tyrosine nitrations for which the consequences are completely unclear. PLoS ONE 7, e34511.
  • Welinder C. and Ekblad L. (2011) Coomassie staining as loading control in Western blot analysis. J. Proteome Res. 10, 14161419.
  • Wenthold R. J., Petralia R. S., Blahos J., II and Niedzielski A. S. (1996) Evidence for multiple AMPA receptor complexes in hippocampal CA1/CA2 neurons. J. Neurosci. 16, 19821989.
  • Yuen E. Y., Liu W., Karatsoreos I. N., Ren Y., Feng J., McEwen B. S. and Yan Z. (2011) Mechanisms for acute stress-induced enhancement of glutamatergic transmission and working memory. Mol. Psychiatry 16, 156170.
  • Zhou X. H., Brakebusch C., Matthies H. et al. (2001) Neurocan is dispensable for brain development. Mol. Cell. Biol. 21, 59705978.