Abstract
Using quantitative analyses, we identified microRNAs (miRNAs) that were abundantly expressed in visual cortex and that responded to dark rearing and/or monocular deprivation. The most substantially altered miRNA, miR-132, was rapidly upregulated after eye opening and was delayed by dark rearing. In vivo inhibition of miR-132 in mice prevented ocular dominance plasticity in identified neurons following monocular deprivation and affected the maturation of dendritic spines, demonstrating its critical role in the plasticity of visual cortex circuits.
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Acknowledgements
We thank J. Sharma and C. Runyan for feedback, G. Kreiman for assistance with data analysis, M. Constantine-Paton and her laboratory for sharing equipment and B. Karki for technical assistance. Supported by US National Eye Institute Ruth L. Kirschstein Postdoctoral Fellowship 1F32EY020066-01 (N.M.), Helmholtz Young Investigator program HZ-NG-607 (D.E.), a Simons Foundation postdoctoral fellowship (A.B.) and US National Institutes of Health EY017098 and EY007023 to M.S.
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N.M. conceived the hypothesis, designed and executed experiments, analyzed the data, and wrote the manuscript. H.S. conducted in vivo two-photon calcium imaging and analyzed the related data. J.C. conducted neonatal virus injections and structural analysis. A.B. carried out slice electrophysiology. A.B., C.L., A.K., B.C., J.C. and D.T. assisted in various experiments, data analysis and figure preparation. J.S. and D.E. constructed and tested lentivirus vectors and S.S.L. performed miRNA microarray experiments. M.S. supervised and orchestrated all of the experiments and wrote the manuscript with N.M.
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Supplementary Figures 1–12, Tables 1–3, Methods and Discussion (PDF 3018 kb)
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Mellios, N., Sugihara, H., Castro, J. et al. miR-132, an experience-dependent microRNA, is essential for visual cortex plasticity. Nat Neurosci 14, 1240–1242 (2011). https://doi.org/10.1038/nn.2909
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DOI: https://doi.org/10.1038/nn.2909
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