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Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After Status Epilepticus
Nuclear-distribution element-like 1 (NDEL1) is associated with the proliferation and migration of neurons. Vascular endothelial growth factor (VEGF) in combination with VEGF receptor-2 (VEGFR-2) regulates the proliferation and migration of neurons. This study was performed to explore undefined alter...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238446/ https://www.ncbi.nlm.nih.gov/pubmed/32423231 http://dx.doi.org/10.1177/1759091420926836 |
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author | Zhu, Lin Dai, Shujuan Lu, Di Xu, Puying Chen, Lu Han, Yanbing Zhong, Lianmei Chang, Lvhua Wu, Qian |
author_facet | Zhu, Lin Dai, Shujuan Lu, Di Xu, Puying Chen, Lu Han, Yanbing Zhong, Lianmei Chang, Lvhua Wu, Qian |
author_sort | Zhu, Lin |
collection | PubMed |
description | Nuclear-distribution element-like 1 (NDEL1) is associated with the proliferation and migration of neurons. Vascular endothelial growth factor (VEGF) in combination with VEGF receptor-2 (VEGFR-2) regulates the proliferation and migration of neurons. This study was performed to explore undefined alterations in the expression levels of NDEL1 and VEGF/VEGFR-2 within the hippocampus after status epilepticus (SE). Following the creation of pilocarpine-induced epilepsy models using adolescent male C57BL/6 mice, Western blotting and reverse transcription quantitative polymerase chain reaction were applied to assess the levels of NDEL1, VEGF, and VEGFR-2 expression in whole hippocampi at 1, 2, 3, and 4 weeks post-SE, respectively. Immunofluorescent labeling was also employed to detect the colocalization of NDEL1 and VEGF in the hippocampus. Our results indicated that NDEL1 and VEGF have similar patterns of upregulation throughout the hippocampus. Upregulation of VEGFR-2 occurred only in the early stages, and the expression decreased shortly afterward. NDEL1 and VEGF were coexpressed in the cornu ammonis 3 pyramidal cell, granular, and polymorph layers of the dentate gyrus in the hippocampus. This study revealed that NDEL1, VEGF, and VEGFR-2 may work together and are involved in the pathophysiology in the hippocampus after SE. |
format | Online Article Text |
id | pubmed-7238446 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-72384462020-06-01 Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After Status Epilepticus Zhu, Lin Dai, Shujuan Lu, Di Xu, Puying Chen, Lu Han, Yanbing Zhong, Lianmei Chang, Lvhua Wu, Qian ASN Neuro Original Article Nuclear-distribution element-like 1 (NDEL1) is associated with the proliferation and migration of neurons. Vascular endothelial growth factor (VEGF) in combination with VEGF receptor-2 (VEGFR-2) regulates the proliferation and migration of neurons. This study was performed to explore undefined alterations in the expression levels of NDEL1 and VEGF/VEGFR-2 within the hippocampus after status epilepticus (SE). Following the creation of pilocarpine-induced epilepsy models using adolescent male C57BL/6 mice, Western blotting and reverse transcription quantitative polymerase chain reaction were applied to assess the levels of NDEL1, VEGF, and VEGFR-2 expression in whole hippocampi at 1, 2, 3, and 4 weeks post-SE, respectively. Immunofluorescent labeling was also employed to detect the colocalization of NDEL1 and VEGF in the hippocampus. Our results indicated that NDEL1 and VEGF have similar patterns of upregulation throughout the hippocampus. Upregulation of VEGFR-2 occurred only in the early stages, and the expression decreased shortly afterward. NDEL1 and VEGF were coexpressed in the cornu ammonis 3 pyramidal cell, granular, and polymorph layers of the dentate gyrus in the hippocampus. This study revealed that NDEL1, VEGF, and VEGFR-2 may work together and are involved in the pathophysiology in the hippocampus after SE. SAGE Publications 2020-05-18 /pmc/articles/PMC7238446/ /pubmed/32423231 http://dx.doi.org/10.1177/1759091420926836 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Original Article Zhu, Lin Dai, Shujuan Lu, Di Xu, Puying Chen, Lu Han, Yanbing Zhong, Lianmei Chang, Lvhua Wu, Qian Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After Status Epilepticus |
title | Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After
Status Epilepticus |
title_full | Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After
Status Epilepticus |
title_fullStr | Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After
Status Epilepticus |
title_full_unstemmed | Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After
Status Epilepticus |
title_short | Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After
Status Epilepticus |
title_sort | role of ndel1 and vegf/vegfr-2 in mouse hippocampus after
status epilepticus |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7238446/ https://www.ncbi.nlm.nih.gov/pubmed/32423231 http://dx.doi.org/10.1177/1759091420926836 |
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