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LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice
Nogo receptor-1 (NgR1) and its ligands inhibit neuronal plasticity and limit functional recovery after brain damage such as ischemic stroke. We have previously shown that lateral olfactory tract usher substance (LOTUS) antagonizes NgR1-mediated signaling. Here, we investigated whether LOTUS enhances...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589167/ https://www.ncbi.nlm.nih.gov/pubmed/28880879 http://dx.doi.org/10.1371/journal.pone.0184258 |
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author | Takase, Hajime Kurihara, Yuji Yokoyama, Taka-akira Kawahara, Nobutaka Takei, Kohtaro |
author_facet | Takase, Hajime Kurihara, Yuji Yokoyama, Taka-akira Kawahara, Nobutaka Takei, Kohtaro |
author_sort | Takase, Hajime |
collection | PubMed |
description | Nogo receptor-1 (NgR1) and its ligands inhibit neuronal plasticity and limit functional recovery after brain damage such as ischemic stroke. We have previously shown that lateral olfactory tract usher substance (LOTUS) antagonizes NgR1-mediated signaling. Here, we investigated whether LOTUS enhances neuronal plasticity and functional recovery after brain focal ischemia in adult mice. Focal ischemic infarcts were induced in wild-type and LOTUS-overexpressing transgenic mice via middle cerebral artery occlusion. Endogenous LOTUS expression was increased in brain and cervical spinal cord of the contralateral side of ischemia in the chronic phase after brain ischemia. LOTUS overexpression accelerated midline-crossing axonal sprouting from the contralateral side to the ipsilateral side of ischemia in the medullar reticular formation and gray matter of denervated cervical spinal cord. Importantly, LOTUS overexpression improved neurological score highly correlated with laterality ratio of corticoreticular fibers of the medulla oblongata, indicating that LOTUS overexpression may overcome the inhibitory environment induced by NgR1 signaling for damaged motor pathway reconstruction after ischemic stroke. Thus, our data suggest that LOTUS overexpression accelerates neuronal plasticity in the brainstem and cervical spinal cord after stroke and LOTUS administration is useful for future therapeutic strategies. |
format | Online Article Text |
id | pubmed-5589167 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-55891672017-09-15 LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice Takase, Hajime Kurihara, Yuji Yokoyama, Taka-akira Kawahara, Nobutaka Takei, Kohtaro PLoS One Research Article Nogo receptor-1 (NgR1) and its ligands inhibit neuronal plasticity and limit functional recovery after brain damage such as ischemic stroke. We have previously shown that lateral olfactory tract usher substance (LOTUS) antagonizes NgR1-mediated signaling. Here, we investigated whether LOTUS enhances neuronal plasticity and functional recovery after brain focal ischemia in adult mice. Focal ischemic infarcts were induced in wild-type and LOTUS-overexpressing transgenic mice via middle cerebral artery occlusion. Endogenous LOTUS expression was increased in brain and cervical spinal cord of the contralateral side of ischemia in the chronic phase after brain ischemia. LOTUS overexpression accelerated midline-crossing axonal sprouting from the contralateral side to the ipsilateral side of ischemia in the medullar reticular formation and gray matter of denervated cervical spinal cord. Importantly, LOTUS overexpression improved neurological score highly correlated with laterality ratio of corticoreticular fibers of the medulla oblongata, indicating that LOTUS overexpression may overcome the inhibitory environment induced by NgR1 signaling for damaged motor pathway reconstruction after ischemic stroke. Thus, our data suggest that LOTUS overexpression accelerates neuronal plasticity in the brainstem and cervical spinal cord after stroke and LOTUS administration is useful for future therapeutic strategies. Public Library of Science 2017-09-07 /pmc/articles/PMC5589167/ /pubmed/28880879 http://dx.doi.org/10.1371/journal.pone.0184258 Text en © 2017 Takase 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Takase, Hajime Kurihara, Yuji Yokoyama, Taka-akira Kawahara, Nobutaka Takei, Kohtaro LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice |
title | LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice |
title_full | LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice |
title_fullStr | LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice |
title_full_unstemmed | LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice |
title_short | LOTUS overexpression accelerates neuronal plasticity after focal brain ischemia in mice |
title_sort | lotus overexpression accelerates neuronal plasticity after focal brain ischemia in mice |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589167/ https://www.ncbi.nlm.nih.gov/pubmed/28880879 http://dx.doi.org/10.1371/journal.pone.0184258 |
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