Cargando…

Scaling of the AIS and Somatodendritic Compartments in α S RGCs

The anatomical properties of the axon initial segment (AIS) are tailored in certain types of CNS neurons to help optimize different aspects of neuronal function. Here, we questioned whether the AISs of retinal ganglion cells (RGC) were similarly customized, and if so, whether they supported specific...

Descripción completa

Detalles Bibliográficos
Autores principales: Raghuram, Vineeth, Werginz, Paul, Fried, Shelley I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6777007/
https://www.ncbi.nlm.nih.gov/pubmed/31611777
http://dx.doi.org/10.3389/fncel.2019.00436
_version_ 1783456546480455680
author Raghuram, Vineeth
Werginz, Paul
Fried, Shelley I.
author_facet Raghuram, Vineeth
Werginz, Paul
Fried, Shelley I.
author_sort Raghuram, Vineeth
collection PubMed
description The anatomical properties of the axon initial segment (AIS) are tailored in certain types of CNS neurons to help optimize different aspects of neuronal function. Here, we questioned whether the AISs of retinal ganglion cells (RGC) were similarly customized, and if so, whether they supported specific RGC functions. To explore this, we measured the AIS properties in alpha sustained RGCs (α S RGCs) of mouse; α S RGCs sizes vary systematically along the nasal temporal axis of the retina, making these cells an attractive population with which to study potential correlations between AIS properties and cell size. Measurements of AIS length as well as distance from the soma revealed that both were scaled to cell size, i.e., cells with large dendritic fields had long AISs that were relatively far from the soma. Within the AIS, the percentage of Na(v)1.6 voltage-gated sodium channels remained highly consistent, regardless of cell size or other AIS properties. Although ON RGCs were slightly larger than OFF cells at any given location of the retina, the level of scaling and relative distribution of voltage-gated sodium channels were highly similar. Computational modeling revealed that AIS scaling influenced spiking thresholds, spike rate as well as the kinetics of individual action potentials, Interestingly, the effect of individual features of the AIS varied for different neuronal functions, e.g., AIS length had a larger effect on the efficacy by which the AIS initiated spike triggered the somatic spike than it did on repetitive spiking. The polarity of the effect varied for different properties, i.e., increases to soma size increased spike threshold while increases to AIS length decreased threshold. Thus, variations in the relative level of scaling for individual components could fine tune threshold or other neuronal functions. Light responses were highly consistent across the full range of cell sizes suggesting that scaling may post-synaptically shape response stability, e.g., in addition to several well-known pre-synaptic contributors.
format Online
Article
Text
id pubmed-6777007
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-67770072019-10-14 Scaling of the AIS and Somatodendritic Compartments in α S RGCs Raghuram, Vineeth Werginz, Paul Fried, Shelley I. Front Cell Neurosci Neuroscience The anatomical properties of the axon initial segment (AIS) are tailored in certain types of CNS neurons to help optimize different aspects of neuronal function. Here, we questioned whether the AISs of retinal ganglion cells (RGC) were similarly customized, and if so, whether they supported specific RGC functions. To explore this, we measured the AIS properties in alpha sustained RGCs (α S RGCs) of mouse; α S RGCs sizes vary systematically along the nasal temporal axis of the retina, making these cells an attractive population with which to study potential correlations between AIS properties and cell size. Measurements of AIS length as well as distance from the soma revealed that both were scaled to cell size, i.e., cells with large dendritic fields had long AISs that were relatively far from the soma. Within the AIS, the percentage of Na(v)1.6 voltage-gated sodium channels remained highly consistent, regardless of cell size or other AIS properties. Although ON RGCs were slightly larger than OFF cells at any given location of the retina, the level of scaling and relative distribution of voltage-gated sodium channels were highly similar. Computational modeling revealed that AIS scaling influenced spiking thresholds, spike rate as well as the kinetics of individual action potentials, Interestingly, the effect of individual features of the AIS varied for different neuronal functions, e.g., AIS length had a larger effect on the efficacy by which the AIS initiated spike triggered the somatic spike than it did on repetitive spiking. The polarity of the effect varied for different properties, i.e., increases to soma size increased spike threshold while increases to AIS length decreased threshold. Thus, variations in the relative level of scaling for individual components could fine tune threshold or other neuronal functions. Light responses were highly consistent across the full range of cell sizes suggesting that scaling may post-synaptically shape response stability, e.g., in addition to several well-known pre-synaptic contributors. Frontiers Media S.A. 2019-09-27 /pmc/articles/PMC6777007/ /pubmed/31611777 http://dx.doi.org/10.3389/fncel.2019.00436 Text en Copyright © 2019 Raghuram, Werginz and Fried. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Raghuram, Vineeth
Werginz, Paul
Fried, Shelley I.
Scaling of the AIS and Somatodendritic Compartments in α S RGCs
title Scaling of the AIS and Somatodendritic Compartments in α S RGCs
title_full Scaling of the AIS and Somatodendritic Compartments in α S RGCs
title_fullStr Scaling of the AIS and Somatodendritic Compartments in α S RGCs
title_full_unstemmed Scaling of the AIS and Somatodendritic Compartments in α S RGCs
title_short Scaling of the AIS and Somatodendritic Compartments in α S RGCs
title_sort scaling of the ais and somatodendritic compartments in α s rgcs
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6777007/
https://www.ncbi.nlm.nih.gov/pubmed/31611777
http://dx.doi.org/10.3389/fncel.2019.00436
work_keys_str_mv AT raghuramvineeth scalingoftheaisandsomatodendriticcompartmentsinasrgcs
AT werginzpaul scalingoftheaisandsomatodendriticcompartmentsinasrgcs
AT friedshelleyi scalingoftheaisandsomatodendriticcompartmentsinasrgcs