Loss-of-function mutations in CNTNAP2 cause a syndromic form of autism spectrum disorder in humans and produce social deficits, repetitive behaviors, and seizures in mice. However, the functional effects of these mutations at cellular and circuit levels remain elusive. Using laser-scanning photostimulation, whole-cell recordings, and electron microscopy, we found a dramatic decrease in excitatory and inhibitory synaptic inputs onto L2/3 pyramidal neurons of the medial prefrontal cortex (mPFC) of Cntnap2 knockout (KO) mice, concurrent with reduced spines and synapses, despite normal dendritic complexity and intrinsic excitability. Moreover, recording of mPFC local field potentials (LFPs) and unit spiking in vivo revealed increased activity in inhibitory neurons, reduced phase-locking to delta and theta oscillations, and delayed phase preference during locomotion. Excitatory neurons showed similar phase modulation changes at delta frequencies. Finally, pairwise correlations increased during immobility in KO mice. Thus, reduced synaptic inputs can yield perturbed temporal coordination of neuronal firing in cortical ensembles.
Reduced Prefrontal Synaptic Connectivity and Disturbed Oscillatory Population Dynamics in the CNTNAP2 Model of Autism.
CNTNAP2自闭症模型中前额叶突触连接减少和振荡群体动力学紊乱
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作者:Lazaro Maria T, Taxidis Jiannis, Shuman Tristan, Bachmutsky Iris, Ikrar Taruna, Santos Rommel, Marcello G Mark, Mylavarapu Apoorva, Chandra Swasty, Foreman Allison, Goli Rachna, Tran Duy, Sharma Nikhil, Azhdam Michelle, Dong Hongmei, Choe Katrina Y, Peñagarikano Olga, Masmanidis Sotiris C, Rácz Bence, Xu Xiangmin, Geschwind Daniel H, Golshani Peyman
| 期刊: | Cell Reports | 影响因子: | 6.900 |
| 时间: | 2019 | 起止号: | 2019 May 28; 27(9):2567-2578 |
| doi: | 10.1016/j.celrep.2019.05.006 | ||
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