author_facet Wu, Jingchuan
He, Junchi
Tian, Xiaocui
Luo, Yuetao
Zhong, Jianjun
Zhang, Hongrong
Li, Hui
Cen, Bo
Jiang, Tao
Sun, Xiaochuan
Wu, Jingchuan
He, Junchi
Tian, Xiaocui
Luo, Yuetao
Zhong, Jianjun
Zhang, Hongrong
Li, Hui
Cen, Bo
Jiang, Tao
Sun, Xiaochuan
author Wu, Jingchuan
He, Junchi
Tian, Xiaocui
Luo, Yuetao
Zhong, Jianjun
Zhang, Hongrong
Li, Hui
Cen, Bo
Jiang, Tao
Sun, Xiaochuan
spellingShingle Wu, Jingchuan
He, Junchi
Tian, Xiaocui
Luo, Yuetao
Zhong, Jianjun
Zhang, Hongrong
Li, Hui
Cen, Bo
Jiang, Tao
Sun, Xiaochuan
Journal of Neurochemistry
microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
Cellular and Molecular Neuroscience
Biochemistry
author_sort wu, jingchuan
spelling Wu, Jingchuan He, Junchi Tian, Xiaocui Luo, Yuetao Zhong, Jianjun Zhang, Hongrong Li, Hui Cen, Bo Jiang, Tao Sun, Xiaochuan 0022-3042 1471-4159 Wiley Cellular and Molecular Neuroscience Biochemistry http://dx.doi.org/10.1111/jnc.14963 <jats:title>Abstract</jats:title><jats:sec><jats:label /><jats:p>The level of microRNA‐9‐5p (miRNA‐9‐5p) in brain tissues is significantly changed after traumatic brain injury (TBI). However, the effect of miRNA‐9‐5p for brain function in TBI has not been elucidated. In this study, a controlled cortical impact model was used to induce TBI in Sprague–Dawley rats, and an oxygen glucose deprivation model was used to mimic the pathological state in vitro. Brain microvascular endothelial cells (BMECs) and astrocytes were extracted from immature Sprague–Dawley rats and cocultured to reconstruct blood–brain barrier (BBB) in vitro. The results show that the level of miRNA‐9‐5p was significantly increased in brain tissues after TBI, and up‐regulation of miRNA9‐5p contributed to the recovery of neurological function. Up‐regulation of miRNA‐9‐5p with miRNA agomir may significantly alleviate apoptosis, neuroinflammation, and BBB damage in rats after TBI. Moreover, a dual luciferase reporter assay confirmed that miRNA‐9‐5p is a post‐transcriptional modulator of Ptch‐1. In in vitro experiments, the results confirmed that up‐regulation of miRNA‐9‐5p with miRNA mimic alleviates cellular apoptosis, inflammatory response, and BBB damage mainly by inhibiting Ptch‐1. In addition, we found that the activation of Hedgehog pathway was accompanied by inhibition of NF‐κB/MMP‐9 pathway in the BMECs treated with miRNA‐9‐5p mimic. Taken together, these results indicate that up‐regulation of miRNA‐9‐5p alleviates BBB damage and neuroinflammatory responses by activating the Hedgehog pathway and inhibiting NF‐κB/MMP‐9 pathway, which promotes the recovery of neurological function after TBI.</jats:p></jats:sec><jats:sec><jats:label /><jats:p> <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/jnc14963-fig-0010-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text> </jats:p></jats:sec> microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury Journal of Neurochemistry
doi_str_mv 10.1111/jnc.14963
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series Journal of Neurochemistry
source_id 49
title microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_unstemmed microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_full microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_fullStr microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_full_unstemmed microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_short microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_sort microrna‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
topic Cellular and Molecular Neuroscience
Biochemistry
url http://dx.doi.org/10.1111/jnc.14963
publishDate 2020
physical 710-726
description <jats:title>Abstract</jats:title><jats:sec><jats:label /><jats:p>The level of microRNA‐9‐5p (miRNA‐9‐5p) in brain tissues is significantly changed after traumatic brain injury (TBI). However, the effect of miRNA‐9‐5p for brain function in TBI has not been elucidated. In this study, a controlled cortical impact model was used to induce TBI in Sprague–Dawley rats, and an oxygen glucose deprivation model was used to mimic the pathological state in vitro. Brain microvascular endothelial cells (BMECs) and astrocytes were extracted from immature Sprague–Dawley rats and cocultured to reconstruct blood–brain barrier (BBB) in vitro. The results show that the level of miRNA‐9‐5p was significantly increased in brain tissues after TBI, and up‐regulation of miRNA9‐5p contributed to the recovery of neurological function. Up‐regulation of miRNA‐9‐5p with miRNA agomir may significantly alleviate apoptosis, neuroinflammation, and BBB damage in rats after TBI. Moreover, a dual luciferase reporter assay confirmed that miRNA‐9‐5p is a post‐transcriptional modulator of Ptch‐1. In in vitro experiments, the results confirmed that up‐regulation of miRNA‐9‐5p with miRNA mimic alleviates cellular apoptosis, inflammatory response, and BBB damage mainly by inhibiting Ptch‐1. In addition, we found that the activation of Hedgehog pathway was accompanied by inhibition of NF‐κB/MMP‐9 pathway in the BMECs treated with miRNA‐9‐5p mimic. Taken together, these results indicate that up‐regulation of miRNA‐9‐5p alleviates BBB damage and neuroinflammatory responses by activating the Hedgehog pathway and inhibiting NF‐κB/MMP‐9 pathway, which promotes the recovery of neurological function after TBI.</jats:p></jats:sec><jats:sec><jats:label /><jats:p> <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/jnc14963-fig-0010-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text> </jats:p></jats:sec>
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author Wu, Jingchuan, He, Junchi, Tian, Xiaocui, Luo, Yuetao, Zhong, Jianjun, Zhang, Hongrong, Li, Hui, Cen, Bo, Jiang, Tao, Sun, Xiaochuan
author_facet Wu, Jingchuan, He, Junchi, Tian, Xiaocui, Luo, Yuetao, Zhong, Jianjun, Zhang, Hongrong, Li, Hui, Cen, Bo, Jiang, Tao, Sun, Xiaochuan, Wu, Jingchuan, He, Junchi, Tian, Xiaocui, Luo, Yuetao, Zhong, Jianjun, Zhang, Hongrong, Li, Hui, Cen, Bo, Jiang, Tao, Sun, Xiaochuan
author_sort wu, jingchuan
container_issue 6
container_start_page 710
container_title Journal of Neurochemistry
container_volume 153
description <jats:title>Abstract</jats:title><jats:sec><jats:label /><jats:p>The level of microRNA‐9‐5p (miRNA‐9‐5p) in brain tissues is significantly changed after traumatic brain injury (TBI). However, the effect of miRNA‐9‐5p for brain function in TBI has not been elucidated. In this study, a controlled cortical impact model was used to induce TBI in Sprague–Dawley rats, and an oxygen glucose deprivation model was used to mimic the pathological state in vitro. Brain microvascular endothelial cells (BMECs) and astrocytes were extracted from immature Sprague–Dawley rats and cocultured to reconstruct blood–brain barrier (BBB) in vitro. The results show that the level of miRNA‐9‐5p was significantly increased in brain tissues after TBI, and up‐regulation of miRNA9‐5p contributed to the recovery of neurological function. Up‐regulation of miRNA‐9‐5p with miRNA agomir may significantly alleviate apoptosis, neuroinflammation, and BBB damage in rats after TBI. Moreover, a dual luciferase reporter assay confirmed that miRNA‐9‐5p is a post‐transcriptional modulator of Ptch‐1. In in vitro experiments, the results confirmed that up‐regulation of miRNA‐9‐5p with miRNA mimic alleviates cellular apoptosis, inflammatory response, and BBB damage mainly by inhibiting Ptch‐1. In addition, we found that the activation of Hedgehog pathway was accompanied by inhibition of NF‐κB/MMP‐9 pathway in the BMECs treated with miRNA‐9‐5p mimic. Taken together, these results indicate that up‐regulation of miRNA‐9‐5p alleviates BBB damage and neuroinflammatory responses by activating the Hedgehog pathway and inhibiting NF‐κB/MMP‐9 pathway, which promotes the recovery of neurological function after TBI.</jats:p></jats:sec><jats:sec><jats:label /><jats:p> <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/jnc14963-fig-0010-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text> </jats:p></jats:sec>
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imprint_str_mv Wiley, 2020
institution DE-Brt1, DE-D161, DE-Zwi2, DE-Gla1, DE-Zi4, DE-15, DE-Pl11, DE-Rs1, DE-105, DE-14, DE-Ch1, DE-L229, DE-D275, DE-Bn3
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spelling Wu, Jingchuan He, Junchi Tian, Xiaocui Luo, Yuetao Zhong, Jianjun Zhang, Hongrong Li, Hui Cen, Bo Jiang, Tao Sun, Xiaochuan 0022-3042 1471-4159 Wiley Cellular and Molecular Neuroscience Biochemistry http://dx.doi.org/10.1111/jnc.14963 <jats:title>Abstract</jats:title><jats:sec><jats:label /><jats:p>The level of microRNA‐9‐5p (miRNA‐9‐5p) in brain tissues is significantly changed after traumatic brain injury (TBI). However, the effect of miRNA‐9‐5p for brain function in TBI has not been elucidated. In this study, a controlled cortical impact model was used to induce TBI in Sprague–Dawley rats, and an oxygen glucose deprivation model was used to mimic the pathological state in vitro. Brain microvascular endothelial cells (BMECs) and astrocytes were extracted from immature Sprague–Dawley rats and cocultured to reconstruct blood–brain barrier (BBB) in vitro. The results show that the level of miRNA‐9‐5p was significantly increased in brain tissues after TBI, and up‐regulation of miRNA9‐5p contributed to the recovery of neurological function. Up‐regulation of miRNA‐9‐5p with miRNA agomir may significantly alleviate apoptosis, neuroinflammation, and BBB damage in rats after TBI. Moreover, a dual luciferase reporter assay confirmed that miRNA‐9‐5p is a post‐transcriptional modulator of Ptch‐1. In in vitro experiments, the results confirmed that up‐regulation of miRNA‐9‐5p with miRNA mimic alleviates cellular apoptosis, inflammatory response, and BBB damage mainly by inhibiting Ptch‐1. In addition, we found that the activation of Hedgehog pathway was accompanied by inhibition of NF‐κB/MMP‐9 pathway in the BMECs treated with miRNA‐9‐5p mimic. Taken together, these results indicate that up‐regulation of miRNA‐9‐5p alleviates BBB damage and neuroinflammatory responses by activating the Hedgehog pathway and inhibiting NF‐κB/MMP‐9 pathway, which promotes the recovery of neurological function after TBI.</jats:p></jats:sec><jats:sec><jats:label /><jats:p> <jats:boxed-text content-type="graphic" position="anchor"><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/png" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/jnc14963-fig-0010-m.png"><jats:alt-text>image</jats:alt-text></jats:graphic></jats:boxed-text> </jats:p></jats:sec> microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury Journal of Neurochemistry
spellingShingle Wu, Jingchuan, He, Junchi, Tian, Xiaocui, Luo, Yuetao, Zhong, Jianjun, Zhang, Hongrong, Li, Hui, Cen, Bo, Jiang, Tao, Sun, Xiaochuan, Journal of Neurochemistry, microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury, Cellular and Molecular Neuroscience, Biochemistry
title microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_full microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_fullStr microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_full_unstemmed microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_short microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_sort microrna‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
title_unstemmed microRNA‐9‐5p alleviates blood–brain barrier damage and neuroinflammation after traumatic brain injury
topic Cellular and Molecular Neuroscience, Biochemistry
url http://dx.doi.org/10.1111/jnc.14963