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Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma

It has been hypothesized that synaptic pruning precedes retinal ganglion cell degeneration in glaucoma, causing early dysfunction to retinal ganglion cells. To begin to assess this, we studied the excitatory synaptic inputs to individual ganglion cells in normal mouse retinas and in retinas with gan...

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Autores principales: Berry, Ryan H., Qu, Juan, John, Simon W. M., Howell, Gareth R., Jakobs, Tatjana C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670161/
https://www.ncbi.nlm.nih.gov/pubmed/26637126
http://dx.doi.org/10.1371/journal.pone.0144341
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author Berry, Ryan H.
Qu, Juan
John, Simon W. M.
Howell, Gareth R.
Jakobs, Tatjana C.
author_facet Berry, Ryan H.
Qu, Juan
John, Simon W. M.
Howell, Gareth R.
Jakobs, Tatjana C.
author_sort Berry, Ryan H.
collection PubMed
description It has been hypothesized that synaptic pruning precedes retinal ganglion cell degeneration in glaucoma, causing early dysfunction to retinal ganglion cells. To begin to assess this, we studied the excitatory synaptic inputs to individual ganglion cells in normal mouse retinas and in retinas with ganglion cell degeneration from glaucoma (DBA/2J), or following an optic nerve crush. Excitatory synapses were labeled by AAV2-mediated transfection of ganglion cells with PSD-95-GFP. After both insults the linear density of synaptic inputs to ganglion cells decreased. In parallel, the dendritic arbors lost complexity. We did not observe any cells that had lost dendritic synaptic input while preserving a normal or near-normal morphology. Within the temporal limits of these observations, dendritic remodeling and synapse pruning thus appear to occur near-simultaneously.
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spelling pubmed-46701612015-12-10 Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma Berry, Ryan H. Qu, Juan John, Simon W. M. Howell, Gareth R. Jakobs, Tatjana C. PLoS One Research Article It has been hypothesized that synaptic pruning precedes retinal ganglion cell degeneration in glaucoma, causing early dysfunction to retinal ganglion cells. To begin to assess this, we studied the excitatory synaptic inputs to individual ganglion cells in normal mouse retinas and in retinas with ganglion cell degeneration from glaucoma (DBA/2J), or following an optic nerve crush. Excitatory synapses were labeled by AAV2-mediated transfection of ganglion cells with PSD-95-GFP. After both insults the linear density of synaptic inputs to ganglion cells decreased. In parallel, the dendritic arbors lost complexity. We did not observe any cells that had lost dendritic synaptic input while preserving a normal or near-normal morphology. Within the temporal limits of these observations, dendritic remodeling and synapse pruning thus appear to occur near-simultaneously. Public Library of Science 2015-12-04 /pmc/articles/PMC4670161/ /pubmed/26637126 http://dx.doi.org/10.1371/journal.pone.0144341 Text en © 2015 Berry 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
Berry, Ryan H.
Qu, Juan
John, Simon W. M.
Howell, Gareth R.
Jakobs, Tatjana C.
Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma
title Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma
title_full Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma
title_fullStr Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma
title_full_unstemmed Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma
title_short Synapse Loss and Dendrite Remodeling in a Mouse Model of Glaucoma
title_sort synapse loss and dendrite remodeling in a mouse model of glaucoma
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4670161/
https://www.ncbi.nlm.nih.gov/pubmed/26637126
http://dx.doi.org/10.1371/journal.pone.0144341
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