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Proc Natl Acad Sci U S A ; 112(24): E3131-40, 2015 Jun 16.
Artículo en Inglés | MEDLINE | ID: mdl-26015564

RESUMEN

During critical periods, all cortical neural circuits are refined to optimize their functional properties. The prevailing notion is that the balance between excitation and inhibition determines the onset and closure of critical periods. In contrast, we show that maturation of silent glutamatergic synapses onto principal neurons was sufficient to govern the duration of the critical period for ocular dominance plasticity in the visual cortex of mice. Specifically, postsynaptic density protein-95 (PSD-95) was absolutely required for experience-dependent maturation of silent synapses, and its absence before the onset of critical periods resulted in lifelong juvenile ocular dominance plasticity. Loss of PSD-95 in the visual cortex after the closure of the critical period reinstated silent synapses, resulting in reopening of juvenile-like ocular dominance plasticity. Additionally, silent synapse-based ocular dominance plasticity was largely independent of the inhibitory tone, whose developmental maturation was independent of PSD-95. Moreover, glutamatergic synaptic transmission onto parvalbumin-positive interneurons was unaltered in PSD-95 KO mice. These findings reveal not only that PSD-95-dependent silent synapse maturation in visual cortical principal neurons terminates the critical period for ocular dominance plasticity but also indicate that, in general, once silent synapses are consolidated in any neural circuit, initial experience-dependent functional optimization and critical periods end.


Asunto(s)
Guanilato-Quinasas/fisiología , Proteínas de la Membrana/fisiología , Red Nerviosa/crecimiento & desarrollo , Red Nerviosa/fisiología , Sinapsis/fisiología , Corteza Visual/crecimiento & desarrollo , Corteza Visual/fisiología , Animales , Mapeo Encefálico , Homólogo 4 de la Proteína Discs Large , Predominio Ocular/fisiología , Femenino , Glutamina/fisiología , Guanilato-Quinasas/deficiencia , Guanilato-Quinasas/genética , Masculino , Proteínas de la Membrana/deficiencia , Proteínas de la Membrana/genética , Ratones , Ratones de la Cepa 129 , Ratones Endogámicos C57BL , Ratones Noqueados , Ratones Transgénicos , Plasticidad Neuronal/fisiología , Receptores AMPA/fisiología
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