Encoding of conditioned fear in central amygdala inhibitory circuits

被引:700
作者
Ciocchi, Stephane [1 ]
Herry, Cyril [1 ]
Grenier, Francois [1 ]
Wolff, Steffen B. E. [1 ]
Letzkus, Johannes J. [1 ]
Vlachos, Ioannis [2 ]
Ehrlich, Ingrid [1 ]
Sprengel, Rolf [3 ]
Deisseroth, Karl [4 ]
Stadler, Michael B. [1 ]
Mueller, Christian [1 ]
Luethi, Andreas [1 ]
机构
[1] Friedrich Miescher Inst Biomed Res, CH-4058 Basel, Switzerland
[2] Bernstein Ctr Computat Neurosci, D-79104 Freiburg, Germany
[3] Max Planck Inst Med Res, Dept Mol Neurobiol, D-69120 Heidelberg, Germany
[4] Stanford Univ, Dept Bioengn, Stanford, CA 94305 USA
基金
奥地利科学基金会; 瑞士国家科学基金会;
关键词
LONG-TERM POTENTIATION; CENTRAL NUCLEUS; SYNAPTIC PLASTICITY; PROJECTION NEURONS; RAT; COMPLEX; ORGANIZATION; FOREBRAIN; TRANSMISSION; MECHANISMS;
D O I
10.1038/nature09559
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The central amygdala (CEA), a nucleus predominantly composed of GABAergic inhibitory neurons, is essential for fear conditioning. How the acquisition and expression of conditioned fear are encoded within CEA inhibitory circuits is not understood. Using in vivo electrophysiological, optogenetic and pharmacological approaches in mice, we show that neuronal activity in the lateral subdivision of the central amygdala (CEl) is required for fear acquisition, whereas conditioned fear responses are driven by output neurons in the medial subdivision (CEm). Functional circuit analysis revealed that inhibitory CEA microcircuits are highly organized and that cell-type-specific plasticity of phasic and tonic activity in the CEl to CEm pathway may gate fear expression and regulate fear generalization. Our results define the functional architecture of CEA microcircuits and their role in the acquisition and regulation of conditioned fear behaviour.
引用
收藏
页码:277 / U239
页数:8
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