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Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2

OBJECTIVE: To assess whether miR-204 and HA affect A549 cell injury induced by lipopolysaccharide. Material and Methods. A549 cells were treated with hirsutanol A, and cell damage was induced by LPS followed by analysis of cell proliferation by CCK-8, cell apoptosis by flow cytometry, apoptosis-rela...

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Autores principales: Li, Shufen, Zhao, Lifen, Li, Xujiong, Shang, Gaiping, Gao, Lijing, Song, Zhuohui, Li, Ting
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654527/
https://www.ncbi.nlm.nih.gov/pubmed/34900201
http://dx.doi.org/10.1155/2021/7404671
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author Li, Shufen
Zhao, Lifen
Li, Xujiong
Shang, Gaiping
Gao, Lijing
Song, Zhuohui
Li, Ting
author_facet Li, Shufen
Zhao, Lifen
Li, Xujiong
Shang, Gaiping
Gao, Lijing
Song, Zhuohui
Li, Ting
author_sort Li, Shufen
collection PubMed
description OBJECTIVE: To assess whether miR-204 and HA affect A549 cell injury induced by lipopolysaccharide. Material and Methods. A549 cells were treated with hirsutanol A, and cell damage was induced by LPS followed by analysis of cell proliferation by CCK-8, cell apoptosis by flow cytometry, apoptosis-related protein expression by western blot, downstream target of miR-20 by dual-luciferase reporter gene, and inflammatory factors by ELISA and PCR. RESULTS: LPS can significantly inhibit the viability of A549 cells, induce cell apoptosis, and promote the release of IL-6, IL-1β, and TNF-α, while HA pretreatment can target FOXK2 by upregulating miR-204 levels, thereby alleviating apoptosis and promoting cell viability and at the same time inhibiting the release of inflammatory factors by inhibiting the activation of NF-κB. CONCLUSIONS: miR-204 participates in the protection of HA acute lung injury by targeting FOXK2.
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spelling pubmed-86545272021-12-09 Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2 Li, Shufen Zhao, Lifen Li, Xujiong Shang, Gaiping Gao, Lijing Song, Zhuohui Li, Ting J Healthc Eng Research Article OBJECTIVE: To assess whether miR-204 and HA affect A549 cell injury induced by lipopolysaccharide. Material and Methods. A549 cells were treated with hirsutanol A, and cell damage was induced by LPS followed by analysis of cell proliferation by CCK-8, cell apoptosis by flow cytometry, apoptosis-related protein expression by western blot, downstream target of miR-20 by dual-luciferase reporter gene, and inflammatory factors by ELISA and PCR. RESULTS: LPS can significantly inhibit the viability of A549 cells, induce cell apoptosis, and promote the release of IL-6, IL-1β, and TNF-α, while HA pretreatment can target FOXK2 by upregulating miR-204 levels, thereby alleviating apoptosis and promoting cell viability and at the same time inhibiting the release of inflammatory factors by inhibiting the activation of NF-κB. CONCLUSIONS: miR-204 participates in the protection of HA acute lung injury by targeting FOXK2. Hindawi 2021-11-30 /pmc/articles/PMC8654527/ /pubmed/34900201 http://dx.doi.org/10.1155/2021/7404671 Text en Copyright © 2021 Shufen Li 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
Li, Shufen
Zhao, Lifen
Li, Xujiong
Shang, Gaiping
Gao, Lijing
Song, Zhuohui
Li, Ting
Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2
title Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2
title_full Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2
title_fullStr Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2
title_full_unstemmed Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2
title_short Mir-204 Regulates LPS-Induced A549 Cell Damage by Targeting FOXK2
title_sort mir-204 regulates lps-induced a549 cell damage by targeting foxk2
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8654527/
https://www.ncbi.nlm.nih.gov/pubmed/34900201
http://dx.doi.org/10.1155/2021/7404671
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