Control of fear by discrete prefrontal GABAergic populations encoding valence-specific information

被引:35
作者
Cummings, Kirstie A. [3 ]
Bayshtok, Sabina [1 ,2 ]
Dong, Tri N. [1 ,2 ,5 ]
Kenny, Paul J. [1 ,2 ,4 ]
Clem, Roger L. [1 ,2 ]
机构
[1] Icahn Sch Med Mt Sinai, Nash Family Dept Neurosci, New York, NY 10029 USA
[2] Icahn Sch Med Mt Sinai, Friedman Brain Inst, New York, NY 10029 USA
[3] Univ Alabama Birmingham, Dept Neurobiol, Sch Med, Birmingham, AL 35233 USA
[4] Icahn Sch Med Mt Sinai, Drug Discovery Inst, New York, NY USA
[5] Icahn Sch Med Mt Sinai, Grad Sch Biomed Sci, New York, NY USA
关键词
SOMATOSTATIN INTERNEURONS; CORTICAL INTERNEURONS; AMYGDALA CIRCUITS; ENGRAM CELLS; MEMORY; DISINHIBITION; OSCILLATIONS; EXPRESSION; RETRIEVAL; ENSEMBLES;
D O I
10.1016/j.neuron.2022.07.004
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Neurons activated by learning have been ascribed the unique potential to encode memory, but the functional contribution of discrete cell types remains poorly understood. In particular, it is unclear whether learning en-gages specific GABAergic interneurons and, if so, whether they differ functionally from interneurons recruited by other experiences. Here, we show that fear conditioning activates a heterogeneous neuronal population in the medial prefrontal cortex (mPFC) that is largely comprised of somatostatin-expressing interneurons (SST-INs). Using intersectional genetic approaches, we demonstrate that fear-learning-activated SST-INs exhibit distinct circuit properties and are selectively reactivated to mediate cue-evoked memory expression. In contrast, an orthogonal population of SST-INs activated by morphine experience exerts opposing control over fear and supports reward-like motivational effects. These results outline an important role for discrete subsets of GABAergic cells in emotional learning and point to an unappreciated capacity for functional specialization among SST-INs.
引用
收藏
页码:3036 / +
页数:23
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