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Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells

BACKGROUND: MicroRNA (miRNA) plays an important role in hepatic stellate cell (HSCs) activation and liver fibrosis. The purpose of this study is to explore the effect of hypoxia on the differential expression of mRNAs and miRNAs in rat HSCs. METHODS: HSC-T6 cells were treated with cobalt chloride (C...

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Autores principales: Zhang, Liting, Gao, Jing, Zhou, Dan, Wang, Xiaojun, Li, Junfeng, Wang, Juan, Chen, Hong, Xie, Xiaodong, Chen, Tuo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506783/
https://www.ncbi.nlm.nih.gov/pubmed/34734003
http://dx.doi.org/10.21037/atm-21-4215
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author Zhang, Liting
Gao, Jing
Zhou, Dan
Wang, Xiaojun
Li, Junfeng
Wang, Juan
Chen, Hong
Xie, Xiaodong
Chen, Tuo
author_facet Zhang, Liting
Gao, Jing
Zhou, Dan
Wang, Xiaojun
Li, Junfeng
Wang, Juan
Chen, Hong
Xie, Xiaodong
Chen, Tuo
author_sort Zhang, Liting
collection PubMed
description BACKGROUND: MicroRNA (miRNA) plays an important role in hepatic stellate cell (HSCs) activation and liver fibrosis. The purpose of this study is to explore the effect of hypoxia on the differential expression of mRNAs and miRNAs in rat HSCs. METHODS: HSC-T6 cells were treated with cobalt chloride (CoCl(2)), and the activity of HSC-T6 cells was measured by the CCK-8 assay. The mRNA expression levels of hypoxia inducible factor-1α (HIF-1α), collagen type I, transforming growth factor-β1 (TGF-β1), and Smad7 were measured by RT-qPCR. The protein expression levels of HIF-1α, Bax, Bcl-2, and caspase-3 were assayed by western blot. We used basal medium and 400 µmol/L CoCl(2) medium to treat HSC-T6 cells for 48 h. Cells were harvested after 48 h to extract RNA. Transcriptome sequencing was performed to investigate differentially expressed miRNAs and mRNAs (fold change >2; P<0.05). Bioinformatics analysis was performed to predict the functions of differentially expressed miRNAs and mRNAs. Further, we used RT-qPCR to detect the expression of mRNAs and miRNAs to confirm the accuracy of sequencing. RESULTS: With the increase of CoCl(2) concentration, the activity of HSC-T6 cells decreased (P<0.05). The mRNA expression levels of HIF-1α, collagen I, TGF-β1, and Smad7, and the protein expressions levels of HIF-1α, Bax, caspase-3, and the Bcl-2/Bax ratio were increased compared with the control group (P<0.05), while the expression of Bcl-2 decreased. A total of 54 miRNAs (20 upregulated and 34 downregulated) and 1,423 mRNAs (685 upregulated and 738 downregulated) were differentially expressed in the 400 µmol/L CoCl(2) medium group compared to the control basal medium group. Further bioinformatics analysis demonstrated that the differentially expressed mRNAs and miRNAs were mainly enriched in the synthesis of extracellular matrix. In addition, we used RT-qPCR to detect the expression of mRNAs and miRNAs to confirm the accuracy of sequencing. CONCLUSIONS: Our results presented the profiles of mRNAs and miRNAs in hypoxia-induced HSC-T6 cells in rats, the signaling pathways, and co-expression networks. These findings may suggest novel insights for the early diagnosis and treatment of HSC activation and liver fibrosis.
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spelling pubmed-85067832021-11-02 Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells Zhang, Liting Gao, Jing Zhou, Dan Wang, Xiaojun Li, Junfeng Wang, Juan Chen, Hong Xie, Xiaodong Chen, Tuo Ann Transl Med Original Article BACKGROUND: MicroRNA (miRNA) plays an important role in hepatic stellate cell (HSCs) activation and liver fibrosis. The purpose of this study is to explore the effect of hypoxia on the differential expression of mRNAs and miRNAs in rat HSCs. METHODS: HSC-T6 cells were treated with cobalt chloride (CoCl(2)), and the activity of HSC-T6 cells was measured by the CCK-8 assay. The mRNA expression levels of hypoxia inducible factor-1α (HIF-1α), collagen type I, transforming growth factor-β1 (TGF-β1), and Smad7 were measured by RT-qPCR. The protein expression levels of HIF-1α, Bax, Bcl-2, and caspase-3 were assayed by western blot. We used basal medium and 400 µmol/L CoCl(2) medium to treat HSC-T6 cells for 48 h. Cells were harvested after 48 h to extract RNA. Transcriptome sequencing was performed to investigate differentially expressed miRNAs and mRNAs (fold change >2; P<0.05). Bioinformatics analysis was performed to predict the functions of differentially expressed miRNAs and mRNAs. Further, we used RT-qPCR to detect the expression of mRNAs and miRNAs to confirm the accuracy of sequencing. RESULTS: With the increase of CoCl(2) concentration, the activity of HSC-T6 cells decreased (P<0.05). The mRNA expression levels of HIF-1α, collagen I, TGF-β1, and Smad7, and the protein expressions levels of HIF-1α, Bax, caspase-3, and the Bcl-2/Bax ratio were increased compared with the control group (P<0.05), while the expression of Bcl-2 decreased. A total of 54 miRNAs (20 upregulated and 34 downregulated) and 1,423 mRNAs (685 upregulated and 738 downregulated) were differentially expressed in the 400 µmol/L CoCl(2) medium group compared to the control basal medium group. Further bioinformatics analysis demonstrated that the differentially expressed mRNAs and miRNAs were mainly enriched in the synthesis of extracellular matrix. In addition, we used RT-qPCR to detect the expression of mRNAs and miRNAs to confirm the accuracy of sequencing. CONCLUSIONS: Our results presented the profiles of mRNAs and miRNAs in hypoxia-induced HSC-T6 cells in rats, the signaling pathways, and co-expression networks. These findings may suggest novel insights for the early diagnosis and treatment of HSC activation and liver fibrosis. AME Publishing Company 2021-09 /pmc/articles/PMC8506783/ /pubmed/34734003 http://dx.doi.org/10.21037/atm-21-4215 Text en 2021 Annals of Translational Medicine. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Zhang, Liting
Gao, Jing
Zhou, Dan
Wang, Xiaojun
Li, Junfeng
Wang, Juan
Chen, Hong
Xie, Xiaodong
Chen, Tuo
Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells
title Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells
title_full Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells
title_fullStr Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells
title_full_unstemmed Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells
title_short Profiles of messenger RNAs and MicroRNAs in hypoxia-induced hepatic stellate cells
title_sort profiles of messenger rnas and micrornas in hypoxia-induced hepatic stellate cells
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8506783/
https://www.ncbi.nlm.nih.gov/pubmed/34734003
http://dx.doi.org/10.21037/atm-21-4215
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