Center for Neuroscience and Department of Neurology of the Second Affiliated Hospital, NHC and CAMS Key Laboratory of Medical Neurobiology, Zhejiang University School of Medicine, Hangzhou 310058, China.
Institute of Brain Science, State Key Laboratory of Medical Neurobiology, and Collaborative Innovation Center for Brain Science, Fudan University, Shanghai 200032, China.
Neuron. 2019 May 8;102(3):668-682.e5. doi: 10.1016/j.neuron.2019.02.026. Epub 2019 Mar 18.
Fear behavior is under tight control of the prefrontal cortex, but the underlying microcircuit mechanism remains elusive. In particular, it is unclear how distinct subtypes of inhibitory interneurons (INs) within prefrontal cortex interact and contribute to fear expression. We employed a social fear conditioning paradigm and induced robust social fear in mice. We found that social fear is characterized by activation of dorsal medial prefrontal cortex (dmPFC) and is largely diminished by dmPFC inactivation. With a combination of in vivo electrophysiological recordings and fiber photometry together with cell-type-specific pharmacogenetics, we further demonstrated that somatostatin (SST) INs suppressed parvalbumin (PV) INs and disinhibited pyramidal cells and consequently enhanced dmPFC output to mediate social fear responses. These results reveal a previously unknown disinhibitory microcircuit in prefrontal cortex through interactions between IN subtypes and suggest that SST INs-mediated disinhibition represents an important circuit mechanism in gating social fear behavior.
恐惧行为受到前额叶皮层的严格控制,但潜在的微电路机制仍难以捉摸。特别是,前额叶皮层中不同抑制性中间神经元 (IN) 亚型如何相互作用并促进恐惧表达尚不清楚。我们采用了社交恐惧条件反射范式,在小鼠中诱导出强烈的社交恐惧。我们发现,社交恐惧的特征是背内侧前额叶皮层 (dmPFC) 的激活,而 dmPFC 的失活则大大减少了社交恐惧。通过结合体内电生理记录和光纤光度法以及细胞类型特异性药理学遗传学,我们进一步证明,生长抑素 (SST) IN 抑制了钙结合蛋白 (PV) IN 并去抑制了锥体神经元,从而增强了 dmPFC 的输出,以介导社交恐惧反应。这些结果揭示了前额叶皮层中以前未知的抑制性微电路,通过 IN 亚型之间的相互作用,并表明 SST IN 介导的去抑制代表了门控社交恐惧行为的重要电路机制。