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The Journal of Physiology
Article . 2012 . Peer-reviewed
License: Wiley Online Library User Agreement
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Neurogliaform cells of amygdala: a source of slow phasic inhibition in the basolateral complex

Authors: Mańko, Mirosława; Bienvenu, Thomas C M; Dalezios, Yannis; Capogna, Marco;

Neurogliaform cells of amygdala: a source of slow phasic inhibition in the basolateral complex

Abstract

Key points The amygdala is a key brain structure implicated in processing emotions and is thought to underlie anxiety‐related behaviours. Interneurons of the basolateral amygdala provide constant silencing of principal cells, and are proven to be active cellular elements during emotional processing. We report here a novel interneuron type of the amygdala, termed neurogliaform cell (NGFC), and study its function by a combination of in vivo and in vitro techniques. NGFCs provide a peculiar cell‐to‐cell form of communication via volume transmission of GABA. In‐depth analysis of specific neuron type is likely to improve the understanding of amygdala circuits in health and disease. Abstract  Synaptic inhibition in the amygdala actively participates in processing emotional information. To improve the understanding of interneurons in amygdala networks it is necessary to characterize the GABAergic cell types, their connectivity and physiological roles. We used a mouse line expressing a green fluorescent protein (GFP) under the neuropeptide Y (NPY) promoter. Paired recordings between presynaptic NPY‐GFP‐expressing (+) cells and postsynaptic principal neurons (PNs) of the basolateral amygdala (BLA) were performed. The NPY‐GFP+ neurons displayed small somata and short dendrites embedded in a cloud of highly arborized axon, suggesting a neurogliaform cell (NGFC) type. We discovered that a NPY‐GFP+ cell evoked a GABAA receptor‐mediated slow inhibitory postsynaptic current (IPSC) in a PN and an autaptic IPSC. The slow kinetics of these IPSCs was likely caused by the low concentration and spillover of extracellular GABA. We also report that NGFCs of the BLA fired action potentials phase‐locked to hippocampal theta oscillations in anaesthetized rats. When this firing was re‐played in NPY+‐NGFCs in vitro, it evoked a transient depression of the IPSCs. Presynaptic GABAB receptors and functional depletion of synaptic vesicles determined this short‐term plasticity. Synaptic contacts made by recorded NGFCs showed close appositions, and rarely identifiable classical synaptic structures. Thus, we report here a novel interneuron type of the amygdala that generates volume transmission of GABA. The peculiar functional mode of NGFCs makes them unique amongst all GABAergic cell types of the amygdala identified so far.

Country
United Kingdom
Keywords

Amygdala/cytology, Action Potentials, GABAergic Neurons/classification, Action Potentials/drug effects, Synaptic Transmission, GABA Antagonists, Interneurons, Animals, gamma-Aminobutyric Acid/metabolism, GABAergic Neurons, Theta Rhythm, Dendrites/physiology, gamma-Aminobutyric Acid, Neuronal Plasticity, Dendrites, Amygdala, Axons, Rats, GABA Antagonists/pharmacology, Inhibitory Postsynaptic Potentials, Synapses, Axons/physiology, Interneurons/classification, Synapses/physiology

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    influence
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    impulse
    This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
48
Top 10%
Top 10%
Top 10%
Green
bronze