Nogo Receptor 1 Limits Ocular Dominance Plasticity but not Turnover of Axonal Boutons in a Model of Amblyopia

• Published in: Cerebral cortex (New York, N.Y. 1991) Vol. 26; no. 5; pp. 1975 - 1985
• Main Authors: Frantz, Michael G, Kast, Ryan J, Dorton, Hilary M, Chapman, Katherine S, McGee, Aaron W
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01-05-2016
• Subjects: Amblyopia - genetics; Amblyopia - physiopathology; Animals; Disease Models, Animal; Dominance, Ocular; Female; Male; Mice; Mice, Inbred C57BL; Mice, Knockout; Neuronal Plasticity; Neurons - physiology; Nogo Receptor 1 - genetics; Nogo Receptor 1 - physiology; Presynaptic Terminals - physiology; Sensory Deprivation; Visual Acuity - physiology; Visual Cortex - cytology; Visual Cortex - physiopathology; in vivo imaging; axon; electrophysiology; bouton; optical imaging; long-term monocular deprivation
• ISSN: 1047-3211; 1460-2199
• DOI: 10.1093/cercor/bhv014

The formation and stability of dendritic spines on excitatory cortical neurons are correlated with adult visual plasticity, yet how the formation, loss, and stability of postsynaptic spines register with that of presynaptic axonal varicosities is unknown. Monocular deprivation has been demonstrated to increase the rate of formation of dendritic spines in visual cortex. However, we find that monocular deprivation does not alter the dynamics of intracortical axonal boutons in visual cortex of either adult wild-type (WT) mice or adult NgR1 mutant (ngr1-/-) mice that retain critical period visual plasticity. Restoring normal vision for a week following long-term monocular deprivation (LTMD), a model of amblyopia, partially restores ocular dominance (OD) in WT and ngr1-/- mice but does not alter the formation or stability of axonal boutons. Both WT and ngr1-/- mice displayed a rapid return of normal OD within 8 days after LTMD as measured with optical imaging of intrinsic signals. In contrast, single-unit recordings revealed that ngr1-/- exhibited greater recovery of OD by 8 days post-LTMD. Our findings support a model of structural plasticity in which changes in synaptic connectivity are largely postsynaptic. In contrast, axonal boutons appear to be stable during changes in cortical circuit function.