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Neuron
Article . 2020 . Peer-reviewed
License: CC BY
Data sources: Crossref
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Neuron
Article
License: CC BY
Data sources: UnpayWall
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PubMed Central
Other literature type . 2020
License: CC BY
Data sources: PubMed Central
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Activity-Dependent Plasticity of Axo-axonic Synapses at the Axon Initial Segment

Authors: Pan-Vazquez, Alejandro; Wefelmeyer, Winnie; Gonzalez Sabater, Victoria; Neves, Guilherme; Burrone, Juan;

Activity-Dependent Plasticity of Axo-axonic Synapses at the Axon Initial Segment

Abstract

The activity-dependent rules that govern the wiring of GABAergic interneurons are not well understood. Chandelier cells (ChCs) are a type of GABAergic interneuron that control pyramidal cell output through axo-axonic synapses that target the axon initial segment. In vivo imaging of ChCs during development uncovered a narrow window (P12-P18) over which axons arborized and formed connections. We found that increases in the activity of either pyramidal cells or individual ChCs during this temporal window result in a reversible decrease in axo-axonic connections. Voltage imaging of GABAergic transmission at the axon initial segment (AIS) showed that axo-axonic synapses were depolarizing during this period. Identical manipulations of network activity in older mice (P40-P46), when ChC synapses are inhibitory, resulted instead in an increase in axo-axonic synapses. We propose that the direction of ChC synaptic plasticity follows homeostatic rules that depend on the polarity of axo-axonic synapses.

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Keywords

Aging, Neuronal Plasticity, Pyramidal Cells, Thyroid Nuclear Factor 1, Presynaptic Terminals, Mice, Transgenic, Somatosensory Cortex, Article, Axons, Mice, Interneurons, Synapses, Animals, Axon Initial Segment, gamma-Aminobutyric Acid

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    popularity
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    influence
    This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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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!
77
Top 1%
Top 10%
Top 1%
Green
hybrid