Cargando…
miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model
Neuronal apoptosis is a major pathological hallmark of the neonatal hypoxic-ischemic brain damage (HIBD); however, the role of miR-7a-2-3p in the regulation of HIBD remains unknown. The purpose of this study was to explore the possible roles of miR-7a-2-3p in brain injury using a hypoxia-ischemia mo...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351497/ https://www.ncbi.nlm.nih.gov/pubmed/30728764 http://dx.doi.org/10.3389/fnins.2019.00016 |
_version_ | 1783390583057809408 |
---|---|
author | Zhang, Zi-Bin Tan, Ya-Xin Zhao, Qiong Xiong, Liu-Lin Liu, Jia Xu, Fei-Fei Xu, Yang Bobrovskaya, Larisa Zhou, Xin-Fu Wang, Ting-Hua |
author_facet | Zhang, Zi-Bin Tan, Ya-Xin Zhao, Qiong Xiong, Liu-Lin Liu, Jia Xu, Fei-Fei Xu, Yang Bobrovskaya, Larisa Zhou, Xin-Fu Wang, Ting-Hua |
author_sort | Zhang, Zi-Bin |
collection | PubMed |
description | Neuronal apoptosis is a major pathological hallmark of the neonatal hypoxic-ischemic brain damage (HIBD); however, the role of miR-7a-2-3p in the regulation of HIBD remains unknown. The purpose of this study was to explore the possible roles of miR-7a-2-3p in brain injury using a hypoxia-ischemia model in rats and oxygen-glucose deprivation (OGD) model in vitro. Firstly, we established the hypoxia-ischemia (HI) model and verified the model using Zea Longa scores and MRI in rats. Next, the changes of miR-7a-2-3p were screened in the ischemic cortex of neonatal rats by qRT-PCR at 12, 48, and 96 h after HIBD. We have found that the expression of miR-7a-2-3p in the HI rats decreased significantly, compared with the sham group (P < 0.01). Then, we established the OGD model in PC12 cells, SH-SY5Y cells and primary cortical neurons in vitro and qRT-PCR was used to confirm the changes of miR-7a-2-3p in these cells after the OGD. In order to determine the function of miR-7a-2-3p, PC12 cells, SH-SY5Y cells and rat primary cortical neurons were randomly divided into normal, OGD, mimic negative control (mimic-NC) and miR-7a-2-3p groups. Then, Tuj1+ (neuronal marker) staining, TUNEL assay (to detect apoptotic cells) and MTT assay (to investigate cell viability) were performed. We have found that the number of PC12 cells, SH-SY5Y cells and cortical neurons in the miR-7a-2-3p groups increased significantly (P < 0.01) in comparison to the OGD groups. The survival of cortical neurons in the miR-7a-2-3p group was improved markedly (P < 0.01), while the apoptosis of neurons in the miR-7a-2-3p group was significantly decreased (P < 0.01), compared with the normal group. Lastly, we investigated the target genes of miR-7a-2-3p by using the prediction databases (miRDB, TargetScan, miRWalk, and miRmap) and verified the target genes with qRT-PCR in the HI rats. Bioinformatics prediction showed that Vimentin (VIM), pleiomorphic adenoma gene 1(PLAG1), dual specificity phosphatase 10 (DUSP10), NAD(P)H dehydrogenase, quinone 1 (NQO1) and tumor necrosis factor receptor superfamily member 1B (TNFRSF1B) might be the targets of miR-7a-2-3p and the qRT-PCR confirmed that VIM increased in the HI rats (P < 0.01). In conclusion, miR-7a-2-3p plays a crucial role in the hypoxic-ischemic injury, and is associated with regulation of VIM. |
format | Online Article Text |
id | pubmed-6351497 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-63514972019-02-06 miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model Zhang, Zi-Bin Tan, Ya-Xin Zhao, Qiong Xiong, Liu-Lin Liu, Jia Xu, Fei-Fei Xu, Yang Bobrovskaya, Larisa Zhou, Xin-Fu Wang, Ting-Hua Front Neurosci Neuroscience Neuronal apoptosis is a major pathological hallmark of the neonatal hypoxic-ischemic brain damage (HIBD); however, the role of miR-7a-2-3p in the regulation of HIBD remains unknown. The purpose of this study was to explore the possible roles of miR-7a-2-3p in brain injury using a hypoxia-ischemia model in rats and oxygen-glucose deprivation (OGD) model in vitro. Firstly, we established the hypoxia-ischemia (HI) model and verified the model using Zea Longa scores and MRI in rats. Next, the changes of miR-7a-2-3p were screened in the ischemic cortex of neonatal rats by qRT-PCR at 12, 48, and 96 h after HIBD. We have found that the expression of miR-7a-2-3p in the HI rats decreased significantly, compared with the sham group (P < 0.01). Then, we established the OGD model in PC12 cells, SH-SY5Y cells and primary cortical neurons in vitro and qRT-PCR was used to confirm the changes of miR-7a-2-3p in these cells after the OGD. In order to determine the function of miR-7a-2-3p, PC12 cells, SH-SY5Y cells and rat primary cortical neurons were randomly divided into normal, OGD, mimic negative control (mimic-NC) and miR-7a-2-3p groups. Then, Tuj1+ (neuronal marker) staining, TUNEL assay (to detect apoptotic cells) and MTT assay (to investigate cell viability) were performed. We have found that the number of PC12 cells, SH-SY5Y cells and cortical neurons in the miR-7a-2-3p groups increased significantly (P < 0.01) in comparison to the OGD groups. The survival of cortical neurons in the miR-7a-2-3p group was improved markedly (P < 0.01), while the apoptosis of neurons in the miR-7a-2-3p group was significantly decreased (P < 0.01), compared with the normal group. Lastly, we investigated the target genes of miR-7a-2-3p by using the prediction databases (miRDB, TargetScan, miRWalk, and miRmap) and verified the target genes with qRT-PCR in the HI rats. Bioinformatics prediction showed that Vimentin (VIM), pleiomorphic adenoma gene 1(PLAG1), dual specificity phosphatase 10 (DUSP10), NAD(P)H dehydrogenase, quinone 1 (NQO1) and tumor necrosis factor receptor superfamily member 1B (TNFRSF1B) might be the targets of miR-7a-2-3p and the qRT-PCR confirmed that VIM increased in the HI rats (P < 0.01). In conclusion, miR-7a-2-3p plays a crucial role in the hypoxic-ischemic injury, and is associated with regulation of VIM. Frontiers Media S.A. 2019-01-23 /pmc/articles/PMC6351497/ /pubmed/30728764 http://dx.doi.org/10.3389/fnins.2019.00016 Text en Copyright © 2019 Zhang, Tan, Zhao, Xiong, Liu, Xu, Xu, Bobrovskaya, Zhou and Wang. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Neuroscience Zhang, Zi-Bin Tan, Ya-Xin Zhao, Qiong Xiong, Liu-Lin Liu, Jia Xu, Fei-Fei Xu, Yang Bobrovskaya, Larisa Zhou, Xin-Fu Wang, Ting-Hua miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model |
title | miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model |
title_full | miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model |
title_fullStr | miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model |
title_full_unstemmed | miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model |
title_short | miRNA-7a-2-3p Inhibits Neuronal Apoptosis in Oxygen-Glucose Deprivation (OGD) Model |
title_sort | mirna-7a-2-3p inhibits neuronal apoptosis in oxygen-glucose deprivation (ogd) model |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6351497/ https://www.ncbi.nlm.nih.gov/pubmed/30728764 http://dx.doi.org/10.3389/fnins.2019.00016 |
work_keys_str_mv | AT zhangzibin mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT tanyaxin mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT zhaoqiong mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT xiongliulin mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT liujia mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT xufeifei mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT xuyang mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT bobrovskayalarisa mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT zhouxinfu mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel AT wangtinghua mirna7a23pinhibitsneuronalapoptosisinoxygenglucosedeprivationogdmodel |