| Literature DB >> 33026181 |
Alessandro Cellerino1,2, Tommaso Pizzorusso1,3,4, Debora Napoli1,3, Leonardo Lupori1, Raffaele Mazziotti4, Giulia Sagona4,5,6, Sara Bagnoli1, Muntaha Samad7, Erika Kelmer Sacramento2, Joanna Kirkpartick2, Elena Putignano3, Siwei Chen7, Eva Terzibasi Tozzini8, Paola Tognini1,9, Pierre Baldi7, Jessica Cf Kwok10,11.
Abstract
Visual cortical circuits show profound plasticity during early life and are later stabilized by molecular "brakes" limiting excessive rewiring beyond a critical period. The mechanisms coordinating the expression of these factors during the transition from development to adulthood remain unknown. We found that miR-29a expression in the visual cortex dramatically increases with age, but it is not experience-dependent. Precocious high levels of miR-29a blocked ocular dominance plasticity and caused an early appearance of perineuronal nets. Conversely, inhibition of miR-29a in adult mice using LNA antagomirs activated ocular dominance plasticity, reduced perineuronal nets, and restored their juvenile chemical composition. Activated adult plasticity had the typical functional and proteomic signature of critical period plasticity. Transcriptomic and proteomic studies indicated that miR-29a manipulation regulates the expression of plasticity brakes in specific cortical circuits. These data indicate that miR-29a is a regulator of the plasticity brakes promoting age-dependent stabilization of visual cortical connections.Entities:
Keywords: DNA methylation; microRNA; ocular dominance plasticity; perineuronal net
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Year: 2020 PMID: 33026181 PMCID: PMC7645255 DOI: 10.15252/embr.202050431
Source DB: PubMed Journal: EMBO Rep ISSN: 1469-221X Impact factor: 8.807