Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneurons

The O-LM cell type mediates feedback inhibition onto hippocampal pyramidal cells and gates information flow in the CA1. Its functions depend on the presence of voltage-gated channels (VGCs), which affect its integrative properties and response to synaptic input. Given the challenges associated with...

Full description

Bibliographic Details
Main Authors: Vladislav eSekulic, Tse-Chiang eChen, J. Josh eLawrence, Frances K. Skinner
Format: Article
Language:English
Published: Frontiers Media S.A. 2015-02-01
Series:Frontiers in Synaptic Neuroscience
Subjects:
Online Access:http://journal.frontiersin.org/Journal/10.3389/fnsyn.2015.00002/full
_version_ 1818470413349421056
author Vladislav eSekulic
Vladislav eSekulic
Tse-Chiang eChen
J. Josh eLawrence
J. Josh eLawrence
Frances K. Skinner
Frances K. Skinner
Frances K. Skinner
author_facet Vladislav eSekulic
Vladislav eSekulic
Tse-Chiang eChen
J. Josh eLawrence
J. Josh eLawrence
Frances K. Skinner
Frances K. Skinner
Frances K. Skinner
author_sort Vladislav eSekulic
collection DOAJ
description The O-LM cell type mediates feedback inhibition onto hippocampal pyramidal cells and gates information flow in the CA1. Its functions depend on the presence of voltage-gated channels (VGCs), which affect its integrative properties and response to synaptic input. Given the challenges associated with determining densities and distributions of VGCs on interneuron dendrites, we take advantage of computational modeling to consider different possibilities. In this work, we focus on hyperpolarization-activated channels (h-channels) in O-LM cells. While h-channels are known to be present in O-LM cells, it is unknown whether they are present on their dendrites. In previous work, we used ensemble modeling techniques with experimental data to obtain insights into potentially important conductance balances. We found that the best O-LM models that included uniformly distributed h-channels in the dendrites could not fully capture the sag response. This led us to examine activation kinetics and non-uniform distributions of h-channels in the present work. In tuning our models, we found that different kinetics and non-uniform distributions could better reproduce experimental O-LM cell responses. In contrast to CA1 pyramidal cells where higher conductance densities of h-channels occur in more distal dendrites, decreasing conductance densities of h-channels away from the soma were observed in O-LM models. Via an illustrative scenario, we showed that having dendritic h-channels clearly speeds up back-propagating action potentials in O-LM cells, unlike when h-channels are present only in the soma. Although the present results were morphology-dependent, our work shows that it should be possible to determine the distributions and characteristics of O-LM cells with recordings and morphologies from the same cell. We hypothesize that h-channels are distributed in O-LM cell dendrites and endow them with particular synaptic integration properties that shape information flow in hippocampus.
first_indexed 2024-04-13T21:37:03Z
format Article
id doaj.art-79b7d6618bbd4d62a708b91a71fb183f
institution Directory Open Access Journal
issn 1663-3563
language English
last_indexed 2024-04-13T21:37:03Z
publishDate 2015-02-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Synaptic Neuroscience
spelling doaj.art-79b7d6618bbd4d62a708b91a71fb183f2022-12-22T02:28:56ZengFrontiers Media S.A.Frontiers in Synaptic Neuroscience1663-35632015-02-01710.3389/fnsyn.2015.00002113143Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneuronsVladislav eSekulic0Vladislav eSekulic1Tse-Chiang eChen2J. Josh eLawrence3J. Josh eLawrence4Frances K. Skinner5Frances K. Skinner6Frances K. Skinner7Toronto Western Research InstituteUniversity of TorontoToronto Western Research InstituteUniversity of MontanaUniversity of MontanaToronto Western Research InstituteUniversity of TorontoUniversity of TorontoThe O-LM cell type mediates feedback inhibition onto hippocampal pyramidal cells and gates information flow in the CA1. Its functions depend on the presence of voltage-gated channels (VGCs), which affect its integrative properties and response to synaptic input. Given the challenges associated with determining densities and distributions of VGCs on interneuron dendrites, we take advantage of computational modeling to consider different possibilities. In this work, we focus on hyperpolarization-activated channels (h-channels) in O-LM cells. While h-channels are known to be present in O-LM cells, it is unknown whether they are present on their dendrites. In previous work, we used ensemble modeling techniques with experimental data to obtain insights into potentially important conductance balances. We found that the best O-LM models that included uniformly distributed h-channels in the dendrites could not fully capture the sag response. This led us to examine activation kinetics and non-uniform distributions of h-channels in the present work. In tuning our models, we found that different kinetics and non-uniform distributions could better reproduce experimental O-LM cell responses. In contrast to CA1 pyramidal cells where higher conductance densities of h-channels occur in more distal dendrites, decreasing conductance densities of h-channels away from the soma were observed in O-LM models. Via an illustrative scenario, we showed that having dendritic h-channels clearly speeds up back-propagating action potentials in O-LM cells, unlike when h-channels are present only in the soma. Although the present results were morphology-dependent, our work shows that it should be possible to determine the distributions and characteristics of O-LM cells with recordings and morphologies from the same cell. We hypothesize that h-channels are distributed in O-LM cell dendrites and endow them with particular synaptic integration properties that shape information flow in hippocampus.http://journal.frontiersin.org/Journal/10.3389/fnsyn.2015.00002/fullDendritesHippocampusInterneuronsmulti-compartment modelIhh-channels
spellingShingle Vladislav eSekulic
Vladislav eSekulic
Tse-Chiang eChen
J. Josh eLawrence
J. Josh eLawrence
Frances K. Skinner
Frances K. Skinner
Frances K. Skinner
Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneurons
Frontiers in Synaptic Neuroscience
Dendrites
Hippocampus
Interneurons
multi-compartment model
Ih
h-channels
title Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneurons
title_full Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneurons
title_fullStr Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneurons
title_full_unstemmed Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneurons
title_short Dendritic distributions of Ih channels in experimentally-derived multi-compartment models of oriens-lacunosum/moleculare (O-LM) hippocampal interneurons
title_sort dendritic distributions of ih channels in experimentally derived multi compartment models of oriens lacunosum moleculare o lm hippocampal interneurons
topic Dendrites
Hippocampus
Interneurons
multi-compartment model
Ih
h-channels
url http://journal.frontiersin.org/Journal/10.3389/fnsyn.2015.00002/full
work_keys_str_mv AT vladislavesekulic dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons
AT vladislavesekulic dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons
AT tsechiangechen dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons
AT jjoshelawrence dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons
AT jjoshelawrence dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons
AT franceskskinner dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons
AT franceskskinner dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons
AT franceskskinner dendriticdistributionsofihchannelsinexperimentallyderivedmulticompartmentmodelsoforienslacunosummoleculareolmhippocampalinterneurons