期刊
JOURNAL OF NEUROSCIENCE
卷 34, 期 7, 页码 2571-2582出版社
SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.4600-13.2014
关键词
electron microscopy; fast-spiking; LTP; monocular deprivation; optogenetic; pyramidal
资金
- National Eye Institute-National Institutes of Health [R01 EY014439]
Inhibition from fast-spiking (FS) interneurons plays a crucial role in shaping cortical response properties and gating developmental periods of activity-dependent plasticity, yet the expression mechanisms underlying FS inhibitory plasticity remain largely unexplored. In layer 4 of visual cortex (V1), monocular deprivation (MD) induces either depression or potentiation of FS to star pyramidal neuron (FS -> SP) synapses, depending on the age of onset (Maffei et al., 2004, 2006). This reversal in the sign (- to +) of plasticity occurs on the cusp of the canonical critical period (CP). To investigate the expression locus behind this switch in sign of inhibitory plasticity, mice underwentMDduring the pre-CP [eye-opening to postnatal day (p) 17] or CP (p22-p25), and FS -> SP synaptic strength within layer 4 was assessed using confocal and immunoelectron microscopy, as well as optogenetic activation of FS cells to probe quantal amplitude at FS -> SP synapses. BriefMDbefore p17 or p25 did not alter the density of FS -> SP contacts. However, at the ultrastructural level, FS -> SP synapses in deprived hemispheres during the CP, but not the pre-CP or in GAD(65) knock-out mice, had larger synapses and increased docked vesicle density compared with synapses from the nondeprived control hemispheres. Moreover, FS -> SP evoked miniature IPSCs increased in deprived hemispheres when MD was initiated during the CP, accompanied by an increase in the density of postsynaptic GABA(A) receptors at FS -> SP synapses. These coordinated changes in FS -> SP synaptic strength define an expression pathway modulating excitatory output during CP plasticity in visual cortex.
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