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miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5

OBJECTIVE: To elucidate the role of microRNA-576 (miRNA-576) in alleviating the deterioration of atherosclerosis (AS) through downregulating krüpple-like factor 5 (KLF5). MATERIALS AND METHODS: The AS model in mice was first constructed. Body weight, inflammation degrees, blood lipid, and relative l...

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Autores principales: Wang, Jing, Zhang, Lihui, Wang, Ting, Li, Caige, Jiao, Lijing, Zhao, Zhansheng, Li, Yongjun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674069/
https://www.ncbi.nlm.nih.gov/pubmed/34925646
http://dx.doi.org/10.1155/2021/5450685
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author Wang, Jing
Zhang, Lihui
Wang, Ting
Li, Caige
Jiao, Lijing
Zhao, Zhansheng
Li, Yongjun
author_facet Wang, Jing
Zhang, Lihui
Wang, Ting
Li, Caige
Jiao, Lijing
Zhao, Zhansheng
Li, Yongjun
author_sort Wang, Jing
collection PubMed
description OBJECTIVE: To elucidate the role of microRNA-576 (miRNA-576) in alleviating the deterioration of atherosclerosis (AS) through downregulating krüpple-like factor 5 (KLF5). MATERIALS AND METHODS: The AS model in mice was first constructed. Body weight, inflammation degrees, blood lipid, and relative levels of KLF5, miRNA-576, caspase-3, and bcl-2 in AS mice and control mice were compared. Dual-luciferase reporter gene assay was performed to evaluate the binding between miRNA-576 and KLF5. RAW264.7 cells were treated with 200 mg/L ox-LDL for establishing in vitro high-fat model. Regulatory effects of miRNA-576/KLF5 on relative levels of β-catenin and inflammatory factors in RAW264.7 cells were explored. RESULTS: Body weight was heavier in AS mice than in controls. Protein levels of KLF5 and caspase-3 were upregulated, while bcl-2 was downregulated in AS mice. In particular, protein level of KLF5 was highly expressed in aortic tissues of AS mice. TC and LDL increased, and HDL decreased in AS mice compared with controls. Inflammatory factor levels were markedly elevated in AS mice. KLF5 was verified to be the target gene binding miRNA-576. Overexpression of miRNA-576 downregulated KLF5, inflammatory factors, and β-catenin in ox-LDL-treated RAW264.7 cells. Regulatory effect of miRNA-576 on the release of inflammatory factors in RAW264.7 cells could be partially abolished by KLF5. CONCLUSIONS: miRNA-576 alleviates malignant progression of AS via downregulating KLF5.
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spelling pubmed-86740692021-12-16 miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5 Wang, Jing Zhang, Lihui Wang, Ting Li, Caige Jiao, Lijing Zhao, Zhansheng Li, Yongjun Dis Markers Research Article OBJECTIVE: To elucidate the role of microRNA-576 (miRNA-576) in alleviating the deterioration of atherosclerosis (AS) through downregulating krüpple-like factor 5 (KLF5). MATERIALS AND METHODS: The AS model in mice was first constructed. Body weight, inflammation degrees, blood lipid, and relative levels of KLF5, miRNA-576, caspase-3, and bcl-2 in AS mice and control mice were compared. Dual-luciferase reporter gene assay was performed to evaluate the binding between miRNA-576 and KLF5. RAW264.7 cells were treated with 200 mg/L ox-LDL for establishing in vitro high-fat model. Regulatory effects of miRNA-576/KLF5 on relative levels of β-catenin and inflammatory factors in RAW264.7 cells were explored. RESULTS: Body weight was heavier in AS mice than in controls. Protein levels of KLF5 and caspase-3 were upregulated, while bcl-2 was downregulated in AS mice. In particular, protein level of KLF5 was highly expressed in aortic tissues of AS mice. TC and LDL increased, and HDL decreased in AS mice compared with controls. Inflammatory factor levels were markedly elevated in AS mice. KLF5 was verified to be the target gene binding miRNA-576. Overexpression of miRNA-576 downregulated KLF5, inflammatory factors, and β-catenin in ox-LDL-treated RAW264.7 cells. Regulatory effect of miRNA-576 on the release of inflammatory factors in RAW264.7 cells could be partially abolished by KLF5. CONCLUSIONS: miRNA-576 alleviates malignant progression of AS via downregulating KLF5. Hindawi 2021-12-08 /pmc/articles/PMC8674069/ /pubmed/34925646 http://dx.doi.org/10.1155/2021/5450685 Text en Copyright © 2021 Jing Wang et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Wang, Jing
Zhang, Lihui
Wang, Ting
Li, Caige
Jiao, Lijing
Zhao, Zhansheng
Li, Yongjun
miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5
title miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5
title_full miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5
title_fullStr miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5
title_full_unstemmed miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5
title_short miRNA-576 Alleviates the Malignant Progression of Atherosclerosis through Downregulating KLF5
title_sort mirna-576 alleviates the malignant progression of atherosclerosis through downregulating klf5
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8674069/
https://www.ncbi.nlm.nih.gov/pubmed/34925646
http://dx.doi.org/10.1155/2021/5450685
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