We investigated the time course of the expression of several activity-dependent genes evoked by visual inputs in the primary visual cortex (V1) in adult marmosets. In order to examine the rapid time course of activity-dependent gene expression, marmosets were first monocularly inactivated by tetrodotoxin (TTX), kept in darkness for two days, and then exposed to various length of light stimulation. Activity-dependent genes including HTR1B, HTR2A, whose activity-dependency were previously reported by us, and well-known immediate early genes (IEGs), c-FOS, ZIF268, and ARC, were examined by in situ hybridization. Using this system, first, we demonstrated the ocular dominance type of gene expression pattern in V1 under this condition. IEGs were expressed in columnar patterns throughout layers II-VI of all the tested monocular marmosets. Second, we showed the regulation of HTR1B and HTR2A expressions by retinal spontaneous activity, because HTR1B and HTR2A mRNA expressions sustained a certain level regardless of visual stimulation and were inhibited by a blockade of the retinal activity with TTX. Third, IEGs dynamically changed its laminar distribution from half an hour to several hours upon a stimulus onset with the unique time course for each gene. The expression patterns of these genes were different in neurons of each layer as well. These results suggest that the regulation of each neuron in the primary visual cortex of marmosets is subjected to different regulation upon the change of activities from retina. It should be related to a highly differentiated laminar structure of marmoset visual systems, reflecting the functions of the activity-dependent gene expression in marmoset V1.
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Univ Trento, Ctr Mind Brain Sci, Mattarello, ItalyUCL, Wellcome Trust Ctr Neuroimaging, London WC1N 3BG, England
Fusca, Marco
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Rees, Geraint
Schwarzkopf, D. Samuel
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UCL, Inst Cognit Neurosci, London WC1N 3AR, England
UCL, Expt Psychol, London WC1H 0AP, EnglandUCL, Wellcome Trust Ctr Neuroimaging, London WC1N 3BG, England
Schwarzkopf, D. Samuel
Barnes, Gareth
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UCL, Wellcome Trust Ctr Neuroimaging, London WC1N 3BG, EnglandUCL, Wellcome Trust Ctr Neuroimaging, London WC1N 3BG, England
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA
Univ Calif Los Angeles, Dept Psychol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA
Ringach, Dario L.
Mineault, Patrick J.
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA
Mineault, Patrick J.
Tring, Elaine
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA
Tring, Elaine
Olivas, Nicholas D.
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA
Olivas, Nicholas D.
Garcia-Junco-Clemente, Pablo
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA
Univ Seville, Inst Biomed Sevilla, IBiS, Hosp Univ Virgen del Roci,CSIC, Seville 41013, Spain
Univ Seville, Dept Fisiol Med & Biofis, Seville 41013, Spain
CIBERNED, Seville 41013, SpainUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA
Garcia-Junco-Clemente, Pablo
Trachtenberg, Joshua T.
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Univ Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USAUniv Calif Los Angeles, David Geffen Sch Med, Dept Neurobiol, Los Angeles, CA 90095 USA