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The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus
Inhibitory interneurons (INs) in the lateral geniculate nucleus (LGN) provide both axonal and dendritic GABA output to thalamocortical relay cells (TCs). Distal parts of the IN dendrites often enter into complex arrangements known as triadic synapses, where the IN dendrite plays a dual role as posts...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182431/ https://www.ncbi.nlm.nih.gov/pubmed/25268996 http://dx.doi.org/10.1371/journal.pone.0107780 |
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author | Allken, Vaneeda Chepkoech, Joy-Loi Einevoll, Gaute T. Halnes, Geir |
author_facet | Allken, Vaneeda Chepkoech, Joy-Loi Einevoll, Gaute T. Halnes, Geir |
author_sort | Allken, Vaneeda |
collection | PubMed |
description | Inhibitory interneurons (INs) in the lateral geniculate nucleus (LGN) provide both axonal and dendritic GABA output to thalamocortical relay cells (TCs). Distal parts of the IN dendrites often enter into complex arrangements known as triadic synapses, where the IN dendrite plays a dual role as postsynaptic to retinal input and presynaptic to TC dendrites. Dendritic GABA release can be triggered by retinal input, in a highly localized process that is functionally isolated from the soma, but can also be triggered by somatically elicited Ca(2+)-spikes and possibly by backpropagating action potentials. Ca(2+)-spikes in INs are predominantly mediated by T-type Ca(2+)-channels (T-channels). Due to the complex nature of the dendritic signalling, the function of the IN is likely to depend critically on how T-channels are distributed over the somatodendritic membrane (T-distribution). To study the relationship between the T-distribution and several IN response properties, we here run a series of simulations where we vary the T-distribution in a multicompartmental IN model with a realistic morphology. We find that the somatic response to somatic current injection is facilitated by a high T-channel density in the soma-region. Conversely, a high T-channel density in the distal dendritic region is found to facilitate dendritic signalling in both the outward direction (increases the response in distal dendrites to somatic input) and the inward direction (the soma responds stronger to distal synaptic input). The real T-distribution is likely to reflect a compromise between several neural functions, involving somatic response patterns and dendritic signalling. |
format | Online Article Text |
id | pubmed-4182431 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-41824312014-10-07 The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus Allken, Vaneeda Chepkoech, Joy-Loi Einevoll, Gaute T. Halnes, Geir PLoS One Research Article Inhibitory interneurons (INs) in the lateral geniculate nucleus (LGN) provide both axonal and dendritic GABA output to thalamocortical relay cells (TCs). Distal parts of the IN dendrites often enter into complex arrangements known as triadic synapses, where the IN dendrite plays a dual role as postsynaptic to retinal input and presynaptic to TC dendrites. Dendritic GABA release can be triggered by retinal input, in a highly localized process that is functionally isolated from the soma, but can also be triggered by somatically elicited Ca(2+)-spikes and possibly by backpropagating action potentials. Ca(2+)-spikes in INs are predominantly mediated by T-type Ca(2+)-channels (T-channels). Due to the complex nature of the dendritic signalling, the function of the IN is likely to depend critically on how T-channels are distributed over the somatodendritic membrane (T-distribution). To study the relationship between the T-distribution and several IN response properties, we here run a series of simulations where we vary the T-distribution in a multicompartmental IN model with a realistic morphology. We find that the somatic response to somatic current injection is facilitated by a high T-channel density in the soma-region. Conversely, a high T-channel density in the distal dendritic region is found to facilitate dendritic signalling in both the outward direction (increases the response in distal dendrites to somatic input) and the inward direction (the soma responds stronger to distal synaptic input). The real T-distribution is likely to reflect a compromise between several neural functions, involving somatic response patterns and dendritic signalling. Public Library of Science 2014-09-30 /pmc/articles/PMC4182431/ /pubmed/25268996 http://dx.doi.org/10.1371/journal.pone.0107780 Text en © 2014 Allken et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Allken, Vaneeda Chepkoech, Joy-Loi Einevoll, Gaute T. Halnes, Geir The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus |
title | The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus |
title_full | The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus |
title_fullStr | The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus |
title_full_unstemmed | The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus |
title_short | The Subcellular Distribution of T-Type Ca(2+) Channels in Interneurons of the Lateral Geniculate Nucleus |
title_sort | subcellular distribution of t-type ca(2+) channels in interneurons of the lateral geniculate nucleus |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4182431/ https://www.ncbi.nlm.nih.gov/pubmed/25268996 http://dx.doi.org/10.1371/journal.pone.0107780 |
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