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A distinct cortical code for socially learned threat
Studies in mice show that observational fear learning is encoded by neurons in the dorsomedial prefrontal cortex in a manner that is distinct from the encoding of fear learned by direct experience.
- Shana E. Silverstein
- , Ruairi O’Sullivan
- & Andrew Holmes
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Top-down control of flight by a non-canonical cortico-amygdala pathway
This study describes a projection from the medial prefrontal cortex to the central amygdala that is involved in the regulation of defensive responses to threat.
- Chandrashekhar D. Borkar
- , Claire E. Stelly
- & Jonathan P. Fadok
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Neural ensemble dynamics underlying a long-term associative memory
Use of a head-mounted miniature microscope in awake, behaving mice reveals that neural ensembles in the basal and lateral amygdala encode associations between conditioned and unconditioned stimuli in a way that matches models of supervised learning.
- Benjamin F. Grewe
- , Jan Gründemann
- & Mark J. Schnitzer
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Projections from neocortex mediate top-down control of memory retrieval
Here, a sparse neuronal projection from a part of the prefrontal cortex, the anterior cingulate, to the hippocampus is identified that, when activated, can elicit memory retrieval in mice.
- Priyamvada Rajasethupathy
- , Sethuraman Sankaran
- & Karl Deisseroth
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Letter |
A temporal shift in the circuits mediating retrieval of fear memory
Dissociating early from late fear memory retrieval in rats reveals that while the projection from the prelimbic prefrontal cortex to the amygdala is critical for fear memory retrieval at early time points, a separate circuit involving the paraventricular region of the dorsal midline thalamus is critical for fear memory retrieval at late time points, establishing the paraventricular region as a critical maintenance/retrieval node during the transition from short- to long-term fear memory.
- Fabricio H. Do-Monte
- , Kelvin Quiñones-Laracuente
- & Gregory J. Quirk
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Letter |
The paraventricular thalamus controls a central amygdala fear circuit
Inhibiting projections from the paraventricular nucleus of the thalamus to a specific division of the amygdala prevents fear conditioning in mice, indicating an important role for the thalamus–amygdala circuit in establishing and maintaining fear responses.
- Mario A. Penzo
- , Vincent Robert
- & Bo Li
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Letter |
Histone H2A.Z subunit exchange controls consolidation of recent and remote memory
The authors identify a specific histone variant as a memory-suppressor that is initially reduced in expression within the hippocampus during memory formation; as a memory is consolidated to the cortex, reduced histone association with specific plasticity genes is observed, promoting stabilization of the memory.
- Iva B. Zovkic
- , Brynna S. Paulukaitis
- & J. David Sweatt
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Amygdala interneuron subtypes control fear learning through disinhibition
Plasticity within neuronal microcircuits is believed to be the substrate of learning, and this study identifies two distinct disinhibitory mechanisms involving interactions between PV+ and SOM+ interneurons that dynamically regulate principal neuron activity in the amygdala and thereby control auditory fear learning.
- Steffen B. E. Wolff
- , Jan Gründemann
- & Andreas Lüthi
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Letter |
Prefrontal parvalbumin interneurons shape neuronal activity to drive fear expression
Single-unit recordings and optogenetic manipulations in mice undergoing auditory fear conditioning show that fear expression is related to the phasic inhibition of prefrontal cortex (PFC) parvalbumin interneurons; inhibition disinhibits PFC projection neurons and synchronizes their firing, leading to fear expression.
- Julien Courtin
- , Fabrice Chaudun
- & Cyril Herry
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Letter |
Optogenetic stimulation of a hippocampal engram activates fear memory recall
The activation of a population of hippocampal neurons thought to encode a specific fear memory is shown to elicit freezing behaviour in mice.
- Xu Liu
- , Steve Ramirez
- & Susumu Tonegawa
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Letter |
Opposite effects of fear conditioning and extinction on dendritic spine remodelling
In mouse frontal cortex, fear conditioning and extinction cause dendritic spine elimination and, respectively, formation to occur on the same dendritic branches in a cue- and location-specific manner.
- Cora Sau Wan Lai
- , Thomas F. Franke
- & Wen-Biao Gan
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A disinhibitory microcircuit for associative fear learning in the auditory cortex
Stimulus convergence and concomitant auditory cortex disinhibition are essential for fear learning.
- Johannes J. Letzkus
- , Steffen B. E. Wolff
- & Andreas Lüthi
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Article |
Genetic dissection of an amygdala microcircuit that gates conditioned fear
The central amygdala relies on inhibitory circuitry to encode fear memories, but how this information is acquired and expressed in these connections is unknown. Two new papers use a combination of cutting-edge technologies to reveal two distinct microcircuits within the central amygdala, one required for fear acquisition and the other critical for conditioned fear responses. Understanding this architecture provides a strong link between activity in a specific circuit and particular behavioural consequences.
- Wulf Haubensak
- , Prabhat S. Kunwar
- & David J. Anderson
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Article |
Encoding of conditioned fear in central amygdala inhibitory circuits
The central amygdala relies on inhibitory circuitry to encode fear memories, but how this information is acquired and expressed in these connections is unknown. Two new papers use a combination of cutting-edge technologies to reveal two distinct microcircuits within the central amygdala, one required for fear acquisition and the other critical for conditioned fear responses. Understanding this architecture provides a strong link between activity in a specific circuit and particular behavioural consequences.
- Stephane Ciocchi
- , Cyril Herry
- & Andreas Lüthi
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News & Views |
Editing out fear
Retrieving a memory initiates a window of vulnerability for that memory. Simple behavioural methods can modify distressing memories during this window, eliminating fear reactions to traumatic reminders.
- Gregory J. Quirk
- & Mohammed R. Milad