Cited by 209Connexins and lens biologyNeuroscience and Neuropharmacology ResearchNeural dynamics and brain function

Gap junctions among dendrites of cortical GABAergic neurons establish a dense and widespread intercolumnar network

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Fukuda, Takaichi, Kosaka, Toshio, Singer, Wolf, Galuske, Ralf A. W.·2006·The Journal of Neuroscience

Abstract

Gap junctions are common between cortical GABAergic interneurons but little is known about their quantitative distribution along dendritic profiles. Here, we provide direct morphological evidence that parvalbumin-containing GABAergic neurons in layer 2/3 of the cat visual cortex form dense and far-ranging networks through dendritic gap junctions. Gap junction-coupled networks of parvalbumin neurons were visualized using connexin36 immunohistochemistry and confocal laser-scanning microscopy (CLSM). The direct correspondence of connexin36-immunopositve puncta and gap junctions was confirmed by examining the same structures in both CLSM and electron microscopy. Single parvalbumin neurons with large somata (> or =200 microm2) formed 60.3 +/- 12.2 (mean +/- SD) gap junctions with other cells whereby these contacts were not restricted to proximal dendrites but occurred at distances of up to 380 microm from the soma. In a Sholl analysis of large-type parvalbumin neurons, 21.9 +/- 7.9 gap junctions were within 50 microm of the soma, 21.7 +/- 7.6 gap junctions in a segment between 50 and 100 microm, 11.2 +/- 4.7 junctions between 100 and 150 microm, and 5.6 +/- 3.6 junctions were in more distal segments. Serially interconnected neurons could be traced laterally in a boundless manner through multiple gap junctions. Comparison to the orientation-preference columns revealed that parvalbumin-immunoreactive cells distribute randomly whereby their large dendritic fields overlap considerably and cover different orientation columns. It is proposed that this dense and homogeneous electrical coupling of interneurons supports the precise synchronization of neuronal populations with differing feature preferences thereby providing a temporal frame for the generation of distributed representations.

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Authors
Fukuda, T., Kosaka, T., Singer, W., & Galuske, R. A. W.
Affiliations
  • Kyushu University (JP)
  • Max Planck Institute for Brain Research (DE)
  • Technische Universität Darmstadt (DE)
Venue
The Journal of Neuroscience
Published
2006-03-29
Volume
26
Issue
13
Pages
3434-3443
ISSN
  • 0270-6474 (ISSN-L)
  • 1529-2401
OpenAlex
W1980161519
Cited by
209
References
63
Citations by year
2026: 1 · 2025: 6 · 2024: 5 · 2023: 4 · 2022: 5 · 2021: 5 · 2020: 3 · 2019: 5 · 2018: 8 · 2017: 9 · 2016: 13 · 2015: 7 · 2014: 16 · 2013: 7 · 2012: 13
FWCI
7.06
Type
journal article
Language
en
Open access
Locations
  • Journal of Neuroscience (publishedVersion, cc-by-nc-sa)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
  • TUbilio (Technical University of Darmstadt) (submittedVersion)
Funders
Alexander von Humboldt-Stiftung
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Connexins and lens biology
  • Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neuroscience and Neuropharmacology Research
  • Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
Keywords
gap junctions, parvalbumin interneurons, GABAergic interneurons, connexin 36, cat visual cortex, layer 2/3, neuronal synchronization, dendritic morphology
MeSH terms
Animals, Cats, Cells, Cultured, Dendrites, Evoked Potentials, Visual, Female, gamma-Aminobutyric Acid, Interneurons, Male, Nerve Net, Visual Cortex, Gap Junctions

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