» Articles » PMID: 27199673

Chandelier Cells in Functional and Dysfunctional Neural Circuits

Overview
Date 2016 May 21
PMID 27199673
Citations 20
Authors
Affiliations
Soon will be listed here.
Abstract

Chandelier cells (ChCs; also called axo-axonic cells) are a specialized GABAergic interneuron subtype that selectively innervates pyramidal neurons at the axon initial segment (AIS), the site of action potential generation. ChC connectivity allows for powerful yet precise modulation of large populations of pyramidal cells, suggesting ChCs have a critical role in brain functions. Dysfunctions in ChC connectivity are associated with brain disorders such as epilepsy and schizophrenia; however, whether this is causative, contributory or compensatory is not known. A likely stumbling block toward mechanistic discoveries and uncovering potential therapeutic targets is the apparent lack of rudimentary understanding of ChCs. For example, whether cortical ChCs are inhibitory or excitatory remains unresolved, and thus whether altered ChC activity results in altered inhibition or excitation is not clear. Recent studies have shed some light onto this excitation-inhibition controversy. In addition, new findings have identified preferential cell-type connectivities established by cortical ChCs, greatly expanding our understanding of the role of ChCs in the cortical microcircuit. Here we aim to bring more attention to ChC connectivity to better understand its role in neural circuits, address whether ChCs are inhibitory or excitatory in light of recent findings and discuss ChC dysfunctions in brain disorders.

Citing Articles

Editorial: Cellular and molecular mechanisms that govern assembly, plasticity, and function of GABAergic inhibitory circuits in the mammalian brain.

Hayano Y, Miyoshi G, Paul A, Taniguchi H Front Cell Neurosci. 2025; 19:1568845.

PMID: 40007758 PMC: 11850328. DOI: 10.3389/fncel.2025.1568845.


Intra-BLA alteration of interneurons' modulation of activity in rats, reveals a dissociation between effects on anxiety symptoms and extinction learning.

Saha R, Wustner L, Chakraborty D, Anunu R, Mandel S, Hazra J Neurobiol Stress. 2024; 33:100681.

PMID: 39512628 PMC: 11541825. DOI: 10.1016/j.ynstr.2024.100681.


Axo-axonic cells in neuropsychiatric disorders: a systematic review.

Vivien J, El Azraoui A, Lheraux C, Lanore F, Aouizerate B, Herry C Front Cell Neurosci. 2023; 17:1212202.

PMID: 37435048 PMC: 10330806. DOI: 10.3389/fncel.2023.1212202.


Synaptic boutons are smaller in chandelier cell cartridges in autism.

Hong T, McBride E, Dufour B, Falcone C, Doan M, Noctor S PLoS One. 2023; 18(4):e0281477.

PMID: 37097993 PMC: 10128992. DOI: 10.1371/journal.pone.0281477.


Distinct patterns of GABAergic interneuron pathology in autism are associated with intellectual impairment and stereotypic behaviors.

Dufour B, McBride E, Bartley T, Juarez P, Martinez-Cerdeno V Autism. 2023; 27(6):1730-1745.

PMID: 36935610 PMC: 10846597. DOI: 10.1177/13623613231154053.


References
1.
Inda M, DeFelipe J, Munoz A . The distribution of chandelier cell axon terminals that express the GABA plasma membrane transporter GAT-1 in the human neocortex. Cereb Cortex. 2006; 17(9):2060-71. DOI: 10.1093/cercor/bhl114. View

2.
Kirmse K, Kummer M, Kovalchuk Y, Witte O, Garaschuk O, Holthoff K . GABA depolarizes immature neurons and inhibits network activity in the neonatal neocortex in vivo. Nat Commun. 2015; 6:7750. DOI: 10.1038/ncomms8750. View

3.
Klausberger T, Magill P, Marton L, Roberts J, Cobden P, Buzsaki G . Brain-state- and cell-type-specific firing of hippocampal interneurons in vivo. Nature. 2003; 421(6925):844-8. DOI: 10.1038/nature01374. View

4.
Dugladze T, Schmitz D, Whittington M, Vida I, Gloveli T . Segregation of axonal and somatic activity during fast network oscillations. Science. 2012; 336(6087):1458-61. DOI: 10.1126/science.1222017. View

5.
Owens D, Boyce L, Davis M, Kriegstein A . Excitatory GABA responses in embryonic and neonatal cortical slices demonstrated by gramicidin perforated-patch recordings and calcium imaging. J Neurosci. 1996; 16(20):6414-23. PMC: 6578913. View