Expression of Perineuronal Nets, Parvalbumin and Protein Tyrosine Phosphatase σ in the Rat Visual Cortex During Development and After BFD

References

• Berardi N, Pizzorusso T, Maffei L. Extracellular matrix and visual cortical plasticity: freeing the synapse. Neuron 2004;44:905–908
   PubMed Web of Science ®Google Scholar
• He HY, Hodos W, Quinlan EM. Visual deprivation reactivates rapid ocular dominance plasticity in adult visual cortex. J Neurosci 2006;26:2951–2955
   PubMed Web of Science ®Google Scholar
• Pizzorusso T, Medini P, Berardi N, Chierzi S, Fawcett JW, Maffei L. Reactivation of ocular dominance plasticity in the adult visual cortex. Science 2002;298:1248–1251
   PubMed Web of Science ®Google Scholar
• Sato M, Stryker MP. Distinctive features of adult ocular dominance plasticity. J Neurosci 2008;28:10278–10286
   PubMed Web of Science ®Google Scholar
• Fagiolini M, Fritschy JM, Löw K, Möhler H, Rudolph U, Hensch TK. Specific GABAA circuits for visual cortical plasticity. Science 2004;303:1681–1683
   PubMed Web of Science ®Google Scholar
• Huang ZJ, Kirkwood A, Pizzorusso T, Porciatti V, Morales B, Bear MF, et al. BDNF regulates the maturation of inhibition and the critical period of plasticity in mouse visual cortex. Cell 1999;98:739–755
   PubMed Web of Science ®Google Scholar
• Grabert J, Wahle P. Visual experience regulates Kv3.1b and Kv3.2 expression in developing rat visual cortex. Neuroscience 2009;158:654–664
   PubMed Web of Science ®Google Scholar
• Shen Y, Tenney AP, Busch SA, Horn KP, Cuascut FX, Liu K, et al. PTPsigma is a receptor for chondroitin sulfate proteoglycan, an inhibitor of neural regeneration. Science 2009;326:592–596
   PubMed Web of Science ®Google Scholar
• Yan H, Grossman A, Wang H, D'Eustachio P, Mossie K, Musacchio JM, et al. A novel receptor tyrosine phosphatase-sigma that is highly expressed in the nervous system. J Biol Chem 1993;268:24880–24886
   PubMed Web of Science ®Google Scholar
• Stepanek L, Stoker AW, Stoeckli E, Bixby JL. Receptor tyrosine phosphatases guide vertebrate motor axons during development. J Neurosci 2005;25:3813–3823
   PubMed Web of Science ®Google Scholar
• Uetani N, Chagnon MJ, Kennedy TE, Iwakura Y, Tremblay ML. Mammalian motoneuron axon targeting requires receptor protein tyrosine phosphatases sigma and delta. J Neurosci 2006;26:5872–5880
   PubMed Web of Science ®Google Scholar
• Johnson KG, McKinnell IW, Stoker AW, Holt CE. Receptor protein tyrosine phosphatases regulate retinal ganglion cell axon outgrowth in the developing Xenopus visual system. J Neurobiol 2001;49:99–117
   PubMedGoogle Scholar
• Ledig MM, Haj F, Bixby JL, Stoker AW, Mueller BK. The receptor tyrosine phosphatase CRYPalpha promotes intraretinal axon growth. J Cell Biol 1999;147:375–388
   PubMed Web of Science ®Google Scholar
• Johnson KG, Van Vactor D. Receptor protein tyrosine phosphatases in nervous system development. Physiol Rev 2003;83:1–24
   PubMedGoogle Scholar
• Duan Y, Giger RJ. A new role for RPTPsigma in spinal cord injury: signaling chondroitin sulfate proteoglycan inhibition. Sci Signal 2010;3:pe6
   PubMed Web of Science ®Google Scholar
• Wang H, Yan H, Canoll PD, Silvennoinen O, Schlessinger J, Musacchio JM. Expression of receptor protein tyrosine phosphatase-sigma (RPTP-sigma) in the nervous system of the developing and adult rat. J Neurosci Res 1995;41:297–310
   PubMed Web of Science ®Google Scholar
• Sapieha PS, Duplan L, Uetani N, Joly S, Tremblay ML, Kennedy TE, et al. Receptor protein tyrosine phosphatase sigma inhibits axon regrowth in the adult injured CNS. Mol Cell Neurosci 2005;28:625–635
   PubMed Web of Science ®Google Scholar
• Zheng S, Yin ZQ, Zeng YX. Developmental profile of tissue plasminogen activator in postnatal Long Evans rat visual cortex. Mol Vis 2008;14:975–982
   PubMed Web of Science ®Google Scholar
• Qin W, Yin ZQ, Wang S, Zhao Y. Effects of binocular form deprivation on the excitatory post-synaptic currents mediated by N-methyl-D-aspartate receptors in rat visual cortex. Clin Experiment Ophthalmol 2004;32:289–293
   PubMed Web of Science ®Google Scholar
• Li Z, Gao C, Huang H, Sun W, Yi H, Fan X, et al. Neurotransmitter phenotype differentiation and synapse formation of neural precursors engrafting in amyloid-β(1-40) injured rat hippocampus. J Alzheimers Dis 2010;21:1233–1247
   PubMed Web of Science ®Google Scholar
• Tropea D, Capsoni S, Tongiorgi E, Giannotta S, Cattaneo A, Domenici L. Mismatch between BDNF mRNA and protein expression in the developing visual cortex: the role of visual experience. Eur J Neurosci 2001;13:709–721
   PubMed Web of Science ®Google Scholar
• Yin ZQ, Crewther SG, Wang C, Crewther DP. Pre- and post-critical period induced reduction of Cat-301 immunoreactivity in the lateral geniculate nucleus and visual cortex of cats Y-blocked as adults or made strabismic as kittens. Mol Vis 2006;12:858–866
   PubMed Web of Science ®Google Scholar
• Ajmo JM, Eakin AK, Hamel MG, Gottschall PE. Discordant localization of WFA reactivity and brevican/ADAMTS-derived fragment in rodent brain. BMC Neurosci 2008;9:14
   PubMed Web of Science ®Google Scholar
• Härtig W, Brauer K, Bigl V, Brückner G. Chondroitin sulfate proteoglycan-immunoreactivity of lectin-labeled perineuronal nets around parvalbumin-containing neurons. Brain Res 1994;635:307–311
   PubMed Web of Science ®Google Scholar
• Sale A, Maya Vetencourt JF, Medini P, Cenni MC, Baroncelli L, De Pasquale R, et al. Environmental enrichment in adulthood promotes amblyopia recovery through a reduction of intracortical inhibition. Nat Neurosci 2007;10:679–681
   PubMed Web of Science ®Google Scholar
• Hof PR, Glezer II, Condé F, Flagg RA, Rubin MB, Nimchinsky EA, et al. Cellular distribution of the calcium-binding proteins parvalbumin, calbindin, and calretinin in the neocortex of mammals: phylogenetic and developmental patterns. J Chem Neuroanat 1999;16:77–116
   PubMed Web of Science ®Google Scholar
• Hada Y, Yamada Y, Imamura K, Mataga N, Watanabe Y, Yamamoto M. Effects of monocular enucleation on parvalbumin in rat visual system during postnatal development. Invest Ophthalmol Vis Sci 1999;40:2535–2545
   PubMed Web of Science ®Google Scholar
• Wegner F, Härtig W, Bringmann A, Grosche J, Wohlfarth K, Zuschratter W, et al. Diffuse perineuronal nets and modified pyramidal cells immunoreactive for glutamate and the GABA(A) receptor alpha1 subunit form a unique entity in rat cerebral cortex. Exp Neurol 2003;184:705–714
   PubMed Web of Science ®Google Scholar
• Härtig W, Derouiche A, Welt K, Brauer K, Grosche J, Mäder M, et al. Cortical neurons immunoreactive for the potassium channel Kv3.1b subunit are predominantly surrounded by perineuronal nets presumed as a buffering system for cations. Brain Res 1999;842:15–29
   PubMed Web of Science ®Google Scholar
• Seeger G, Lüth HJ, Winkelmann E, Brauer K. Distribution patterns of Wisteria floribunda agglutinin binding sites and parvalbumin-immunoreactive neurons in the human visual cortex: a double-labelling study. J Hirnforsch 1996;37:351–366
   PubMedGoogle Scholar
• Fry EJ, Chagnon MJ, López-Vales R, Tremblay ML, David S. Corticospinal tract regeneration after spinal cord injury in receptor protein tyrosine phosphatase sigma deficient mice. Glia 2010;58:423–433
   PubMed Web of Science ®Google Scholar
• Schaapveld RQ, van den Maagdenberg AM, Schepens JT, Weghuis DO, Geurts van Kessel A, Wieringa B, et al. The mouse gene Ptprf encoding the leukocyte common antigen-related molecule LAR: cloning, characterization, and chromosomal localization. Genomics 1995;27:124–130
   PubMed Web of Science ®Google Scholar
• Kwon SK, Woo J, Kim SY, Kim H, Kim E. Trans-synaptic adhesions between netrin-G ligand-3 (NGL-3) and receptor tyrosine phosphatases LAR, protein-tyrosine phosphatase delta (PTPdelta), and PTPsigma via specific domains regulate excitatory synapse formation. J Biol Chem 2010;285:13966–13978
   PubMed Web of Science ®Google Scholar
• Batt J, Asa S, Fladd C, Rotin D. Pituitary, pancreatic and gut neuroendocrine defects in protein tyrosine phosphatase-sigma-deficient mice. Mol Endocrinol 2002;16:155–169
   PubMedGoogle Scholar
• Kurihara D, Yamashita T. Chondroitin sulfate proteoglycans down-regulate spine formation in cortical neurons by targeting tropomyosin-related kinase B (TrkB) protein. J Biol Chem 2012;287:13822–13828
   PubMed Web of Science ®Google Scholar
• Gorba T, Wahle P. Expression of TrkB and TrkC but not BDNF mRNA in neurochemically identified interneurons in rat visual cortex in vivo and in organotypic cultures. Eur J Neurosci 1999;11:1179–1190
   PubMed Web of Science ®Google Scholar
• Jiang B, Kitamura A, Yasuda H, Sohya K, Maruyama A, Yanagawa Y, et al. Brain-derived neurotrophic factor acutely depresses excitatory synaptic transmission to GABAergic neurons in visual cortical slices. Eur J Neurosci 2004;20:709–718
   PubMed Web of Science ®Google Scholar
• Klausberger T, Roberts JD, Somogyi P. Cell type- and input-specific differences in the number and subtypes of synaptic GABA(A) receptors in the hippocampus. J Neurosci 2002;22:2513–2521
   PubMed Web of Science ®Google Scholar
• Takahashi H, Arstikaitis P, Prasad T, Bartlett TE, Wang YT, Murphy TH, et al. Postsynaptic TrkC and presynaptic PTPσ function as a bidirectional excitatory synaptic organizing complex. Neuron 2011;69:287–303
   PubMed Web of Science ®Google Scholar