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Immune response in the eye following epileptic seizures

BACKGROUND: Epileptic seizures are associated with an immune response in the brain. However, it is not known whether it can extend to remote areas of the brain, such as the eyes. Hence, we investigated whether epileptic seizures induce inflammation in the retina. METHODS: Adult rats underwent electr...

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Autores principales: Ahl, Matilda, Avdic, Una, Skoug, Cecilia, Ali, Idrish, Chugh, Deepti, Johansson, Ulrica Englund, Ekdahl, Christine T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922060/
https://www.ncbi.nlm.nih.gov/pubmed/27346214
http://dx.doi.org/10.1186/s12974-016-0618-3
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author Ahl, Matilda
Avdic, Una
Skoug, Cecilia
Ali, Idrish
Chugh, Deepti
Johansson, Ulrica Englund
Ekdahl, Christine T
author_facet Ahl, Matilda
Avdic, Una
Skoug, Cecilia
Ali, Idrish
Chugh, Deepti
Johansson, Ulrica Englund
Ekdahl, Christine T
author_sort Ahl, Matilda
collection PubMed
description BACKGROUND: Epileptic seizures are associated with an immune response in the brain. However, it is not known whether it can extend to remote areas of the brain, such as the eyes. Hence, we investigated whether epileptic seizures induce inflammation in the retina. METHODS: Adult rats underwent electrically induced temporal status epilepticus, and the eyes were studied 6 h, 1, and 7 weeks later with biochemical and immunohistochemical analyses. An additional group of animals received CX3CR1 antibody intracerebroventricularly for 6 weeks after status epilepticus. RESULTS: Biochemical analyses and immunohistochemistry revealed no increased cell death and unaltered expression of several immune-related cytokines and chemokines as well as no microglial activation, 6 h post-status epilepticus compared to non-stimulated controls. At 1 week, again, retinal cytoarchitecture appeared normal and there was no cell death or micro- or macroglial reaction, apart from a small decrease in interleukin-10. However, at 7 weeks, even if the cytoarchitecture remained normal and no ongoing cell death was detected, the numbers of microglia were increased ipsi- and contralateral to the epileptic focus. The microglia remained within the synaptic layers but often in clusters and with more processes extending into the outer nuclear layer. Morphological analyses revealed a decrease in surveying and an increase in activated microglia. In addition, increased levels of the chemokine KC/GRO and cytokine interleukin-1β were found. Furthermore, macroglial activation was noted in the inner retina. No alterations in numbers of phagocytic cells, infiltrating macrophages, or vascular pericytes were observed. Post-synaptic density-95 cluster intensity was reduced in the outer nuclear layer, reflecting seizure-induced synaptic changes without disrupted cytoarchitecture in areas with increased microglial activation. The retinal gliosis was decreased by a CX3CR1 immune modulation known to reduce gliosis within epileptic foci, suggesting a common immunological reaction. CONCLUSIONS: Our results are the first evidence that epileptic seizures induce an immune response in the retina. It has a potential to become a novel non-invasive tool for detecting brain inflammation through the eyes.
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spelling pubmed-49220602016-06-28 Immune response in the eye following epileptic seizures Ahl, Matilda Avdic, Una Skoug, Cecilia Ali, Idrish Chugh, Deepti Johansson, Ulrica Englund Ekdahl, Christine T J Neuroinflammation Research BACKGROUND: Epileptic seizures are associated with an immune response in the brain. However, it is not known whether it can extend to remote areas of the brain, such as the eyes. Hence, we investigated whether epileptic seizures induce inflammation in the retina. METHODS: Adult rats underwent electrically induced temporal status epilepticus, and the eyes were studied 6 h, 1, and 7 weeks later with biochemical and immunohistochemical analyses. An additional group of animals received CX3CR1 antibody intracerebroventricularly for 6 weeks after status epilepticus. RESULTS: Biochemical analyses and immunohistochemistry revealed no increased cell death and unaltered expression of several immune-related cytokines and chemokines as well as no microglial activation, 6 h post-status epilepticus compared to non-stimulated controls. At 1 week, again, retinal cytoarchitecture appeared normal and there was no cell death or micro- or macroglial reaction, apart from a small decrease in interleukin-10. However, at 7 weeks, even if the cytoarchitecture remained normal and no ongoing cell death was detected, the numbers of microglia were increased ipsi- and contralateral to the epileptic focus. The microglia remained within the synaptic layers but often in clusters and with more processes extending into the outer nuclear layer. Morphological analyses revealed a decrease in surveying and an increase in activated microglia. In addition, increased levels of the chemokine KC/GRO and cytokine interleukin-1β were found. Furthermore, macroglial activation was noted in the inner retina. No alterations in numbers of phagocytic cells, infiltrating macrophages, or vascular pericytes were observed. Post-synaptic density-95 cluster intensity was reduced in the outer nuclear layer, reflecting seizure-induced synaptic changes without disrupted cytoarchitecture in areas with increased microglial activation. The retinal gliosis was decreased by a CX3CR1 immune modulation known to reduce gliosis within epileptic foci, suggesting a common immunological reaction. CONCLUSIONS: Our results are the first evidence that epileptic seizures induce an immune response in the retina. It has a potential to become a novel non-invasive tool for detecting brain inflammation through the eyes. BioMed Central 2016-06-27 /pmc/articles/PMC4922060/ /pubmed/27346214 http://dx.doi.org/10.1186/s12974-016-0618-3 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Ahl, Matilda
Avdic, Una
Skoug, Cecilia
Ali, Idrish
Chugh, Deepti
Johansson, Ulrica Englund
Ekdahl, Christine T
Immune response in the eye following epileptic seizures
title Immune response in the eye following epileptic seizures
title_full Immune response in the eye following epileptic seizures
title_fullStr Immune response in the eye following epileptic seizures
title_full_unstemmed Immune response in the eye following epileptic seizures
title_short Immune response in the eye following epileptic seizures
title_sort immune response in the eye following epileptic seizures
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4922060/
https://www.ncbi.nlm.nih.gov/pubmed/27346214
http://dx.doi.org/10.1186/s12974-016-0618-3
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