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  Elimination of Inhibitory Synapses Is a Major Component of Adult Ocular Dominance Plasticity

van Versendaal, D., Rajendran, R., Saiepour, M. H., Klooster, J., Smit-Rigter, L., Sommeijer, J.-P., et al. (2012). Elimination of Inhibitory Synapses Is a Major Component of Adult Ocular Dominance Plasticity. NEURON, 74(2), 374-383. doi:10.1016/j.neuron.2012.03.015.

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van Versendaal, Danielle1, Autor
Rajendran, Rajeev1, Autor
Saiepour, M. Hadi1, Autor
Klooster, Jan1, Autor
Smit-Rigter, Laura1, Autor
Sommeijer, Jean-Pierre1, Autor
De Zeeuw, Chris I.1, Autor
Hofer, Sonja2, Autor           
Heime, J. Alexander1, Autor
Levelt, Christiaan N.1, Autor
Affiliations:
1External Organizations, ou_persistent22              
2Department: Cellular and Systems Neurobiology / Bonhoeffer, MPI of Neurobiology, Max Planck Society, ou_1113545              

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Schlagwörter: EXPERIENCE-DEPENDENT PLASTICITY; GABA(A) RECEPTOR SUBTYPES; MONKEY STRIATE CORTEX; MOUSE VISUAL-CORTEX; DENDRITIC SPINES; IN-VIVO; GABAERGIC SYNAPSES; QUANTITATIVE DISTRIBUTION; INTRACORTICAL INHIBITION; CORTICAL-NEURONS
 Zusammenfassung: During development, cortical plasticity is associated with the rearrangement of excitatory connections. While these connections become more stable with age, plasticity can still be induced in the adult cortex. Here we provide evidence that structural plasticity of inhibitory synapses onto pyramidal neurons is a major component of plasticity in the adult neocortex. In vivo two-photon imaging was used to monitor the formation and elimination of fluorescently labeled inhibitory structures on pyramidal neurons. We find that ocular dominance plasticity in the adult visual cortex is associated with rapid inhibitory synapse loss, especially of those present on dendritic spines. This occurs not only with monocular deprivation but also with subsequent restoration of binocular vision. We propose that in the adult visual cortex the experience-induced loss of inhibition may effectively strengthen specific visual inputs with limited need for rearranging the excitatory circuitry.

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Sprache(n): eng - English
 Datum: 2012-04-26
 Publikationsstatus: Erschienen
 Seiten: 10
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: ISI: 000303361800017
DOI: 10.1016/j.neuron.2012.03.015
 Art des Abschluß: -

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Titel: NEURON
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: 600 TECHNOLOGY SQUARE, 5TH FLOOR, CAMBRIDGE, MA 02139 USA : CELL PRESS
Seiten: - Band / Heft: 74 (2) Artikelnummer: - Start- / Endseite: 374 - 383 Identifikator: ISSN: 0896-6273