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...

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Main Authors: Lin Zhu, Shujuan Dai, Di Lu, Puying Xu, Lu Chen, Yanbing Han, Lianmei Zhong, Lvhua Chang, Qian Wu
Format: Article
Language:English
Published: SAGE Publishing 2020-05-01
Series:ASN Neuro
Online Access:https://doi.org/10.1177/1759091420926836
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spelling doaj-eb474eb5d34e4b8fb231863b11cfa7532020-11-25T03:03:34ZengSAGE PublishingASN Neuro1759-09142020-05-011210.1177/1759091420926836Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After Status EpilepticusLin ZhuShujuan DaiDi LuPuying XuLu ChenYanbing HanLianmei ZhongLvhua ChangQian WuNuclear-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.https://doi.org/10.1177/1759091420926836
collection DOAJ
language English
format Article
sources DOAJ
author Lin Zhu
Shujuan Dai
Di Lu
Puying Xu
Lu Chen
Yanbing Han
Lianmei Zhong
Lvhua Chang
Qian Wu
spellingShingle Lin Zhu
Shujuan Dai
Di Lu
Puying Xu
Lu Chen
Yanbing Han
Lianmei Zhong
Lvhua Chang
Qian Wu
Role of NDEL1 and VEGF/VEGFR-2 in Mouse Hippocampus After Status Epilepticus
ASN Neuro
author_facet Lin Zhu
Shujuan Dai
Di Lu
Puying Xu
Lu Chen
Yanbing Han
Lianmei Zhong
Lvhua Chang
Qian Wu
author_sort Lin Zhu
title 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_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_sort role of ndel1 and vegf/vegfr-2 in mouse hippocampus after status epilepticus
publisher SAGE Publishing
series ASN Neuro
issn 1759-0914
publishDate 2020-05-01
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.
url https://doi.org/10.1177/1759091420926836
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