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MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1

Cerebral aneurysm (CA) is a common brain disease, and the development of cerebral aneurysm is driven by inflammation and hemodynamic stress. MicroRNA (miR)-124-5p is reported to be associated with inflammatory response in brain disease such as cerebral ischemia-reperfusion injury. However, the funct...

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Autores principales: Wang, Ru-Ke, Sun, Yuan-Yuan, Li, Guang-You, Yang, Hua-Tang, Liu, Xiu-Jie, Li, Ke-Feng, Zhu, Xu, Yu, Guo-Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393823/
https://www.ncbi.nlm.nih.gov/pubmed/34504617
http://dx.doi.org/10.3892/etm.2021.10606
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author Wang, Ru-Ke
Sun, Yuan-Yuan
Li, Guang-You
Yang, Hua-Tang
Liu, Xiu-Jie
Li, Ke-Feng
Zhu, Xu
Yu, Guo-Yuan
author_facet Wang, Ru-Ke
Sun, Yuan-Yuan
Li, Guang-You
Yang, Hua-Tang
Liu, Xiu-Jie
Li, Ke-Feng
Zhu, Xu
Yu, Guo-Yuan
author_sort Wang, Ru-Ke
collection PubMed
description Cerebral aneurysm (CA) is a common brain disease, and the development of cerebral aneurysm is driven by inflammation and hemodynamic stress. MicroRNA (miR)-124-5p is reported to be associated with inflammatory response in brain disease such as cerebral ischemia-reperfusion injury. However, the function and molecular mechanism of miR-124-5p in CA are not clear, thus, the effects of miR-124-5p on inflammatory response in CA were explored. Firstly, the expression of miR-124-5p in the peripheral blood of patients with CA and the control group was detected by reverse transcription-quantitative PCR. Then, the human umbilical vein endothelial cells (HUVECs) were used as an in vitro model system and stimulated with interleukin (IL)-1β to simulate the inflammatory environment of CA, and the expression of miR-124-5p was detected. Next, the effect of miR-124-5p on the migration and invasion of HUVECs was detected using Transwell assays. Meanwhile, the function of miR-124-5p on various inflammatory factors was determined by western blotting and enzyme-linked immunosorbent assay (ELISA). Next, the TargetScan website was used to predict FoxO1 as a target gene of miR-124-5p, and this target association was validated by double luciferase reporter assay and western blotting. Finally, the interaction of miR-124-5p with FoxO1 in CA was measured by Transwell western blotting and ELISA assays. The results showed that the expression level of miR-124-5p in the peripheral blood of patients with CA was lower compared with that of control group, and the miR-124-5p in HUVECs stimulated by IL-1β was less compared with that in normal HUVECs. Besides, miR-124-5p could inhibit the migration and invasion abilities of HUVECs and the release of inflammatory factors. Additionally, the overexpression of miR-124-5p was able to inhibit the expression of FoxO1. miR-124-5p-inhibitor promoted the migration and invasion of HUVECs, as well as inflammatory response, which was weakened following the introduction of FoxO1 small interfering RNA. Overall, the present study demonstrated that miR-124-5p could prevent the occurrence and development of cerebral aneurysm by downregulating the expression of FoxO1.
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spelling pubmed-83938232021-09-08 MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1 Wang, Ru-Ke Sun, Yuan-Yuan Li, Guang-You Yang, Hua-Tang Liu, Xiu-Jie Li, Ke-Feng Zhu, Xu Yu, Guo-Yuan Exp Ther Med Articles Cerebral aneurysm (CA) is a common brain disease, and the development of cerebral aneurysm is driven by inflammation and hemodynamic stress. MicroRNA (miR)-124-5p is reported to be associated with inflammatory response in brain disease such as cerebral ischemia-reperfusion injury. However, the function and molecular mechanism of miR-124-5p in CA are not clear, thus, the effects of miR-124-5p on inflammatory response in CA were explored. Firstly, the expression of miR-124-5p in the peripheral blood of patients with CA and the control group was detected by reverse transcription-quantitative PCR. Then, the human umbilical vein endothelial cells (HUVECs) were used as an in vitro model system and stimulated with interleukin (IL)-1β to simulate the inflammatory environment of CA, and the expression of miR-124-5p was detected. Next, the effect of miR-124-5p on the migration and invasion of HUVECs was detected using Transwell assays. Meanwhile, the function of miR-124-5p on various inflammatory factors was determined by western blotting and enzyme-linked immunosorbent assay (ELISA). Next, the TargetScan website was used to predict FoxO1 as a target gene of miR-124-5p, and this target association was validated by double luciferase reporter assay and western blotting. Finally, the interaction of miR-124-5p with FoxO1 in CA was measured by Transwell western blotting and ELISA assays. The results showed that the expression level of miR-124-5p in the peripheral blood of patients with CA was lower compared with that of control group, and the miR-124-5p in HUVECs stimulated by IL-1β was less compared with that in normal HUVECs. Besides, miR-124-5p could inhibit the migration and invasion abilities of HUVECs and the release of inflammatory factors. Additionally, the overexpression of miR-124-5p was able to inhibit the expression of FoxO1. miR-124-5p-inhibitor promoted the migration and invasion of HUVECs, as well as inflammatory response, which was weakened following the introduction of FoxO1 small interfering RNA. Overall, the present study demonstrated that miR-124-5p could prevent the occurrence and development of cerebral aneurysm by downregulating the expression of FoxO1. D.A. Spandidos 2021-10 2021-08-13 /pmc/articles/PMC8393823/ /pubmed/34504617 http://dx.doi.org/10.3892/etm.2021.10606 Text en Copyright: © Wang et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
Wang, Ru-Ke
Sun, Yuan-Yuan
Li, Guang-You
Yang, Hua-Tang
Liu, Xiu-Jie
Li, Ke-Feng
Zhu, Xu
Yu, Guo-Yuan
MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1
title MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1
title_full MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1
title_fullStr MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1
title_full_unstemmed MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1
title_short MicroRNA-124-5p delays the progression of cerebral aneurysm by regulating FoxO1
title_sort microrna-124-5p delays the progression of cerebral aneurysm by regulating foxo1
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8393823/
https://www.ncbi.nlm.nih.gov/pubmed/34504617
http://dx.doi.org/10.3892/etm.2021.10606
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