Cargando…

miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1

The present study aimed to explore the biological functions of microRNA (miR)-146b-5p and homeodomain interacting protein kinase 1 (HIPK1) in the progression of hepatic fibrosis (HF) and to identify the underlying mechanism. A rat HF model was established by administering a subcutaneous injection of...

Descripción completa

Detalles Bibliográficos
Autores principales: Xie, Junfeng, Cheng, Na, Huang, Zhanchao, Shu, Xu, Xiang, Tianxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257962/
https://www.ncbi.nlm.nih.gov/pubmed/35837064
http://dx.doi.org/10.3892/etm.2022.11474
_version_ 1784741434689060864
author Xie, Junfeng
Cheng, Na
Huang, Zhanchao
Shu, Xu
Xiang, Tianxin
author_facet Xie, Junfeng
Cheng, Na
Huang, Zhanchao
Shu, Xu
Xiang, Tianxin
author_sort Xie, Junfeng
collection PubMed
description The present study aimed to explore the biological functions of microRNA (miR)-146b-5p and homeodomain interacting protein kinase 1 (HIPK1) in the progression of hepatic fibrosis (HF) and to identify the underlying mechanism. A rat HF model was established by administering a subcutaneous injection of carbon tetrachloride (CCl(4)). Relative levels of miR-146b-5p and HIPK1 in fibrotic rat liver tissues and the rat hepatic stellate cell (HSC) line HSC-T6 were measured by quantitative reverse transcription PCR, western blotting and immunohistochemistry. Following activation of HSC-T6 cells by lipopolysaccharide (LPS) induction, cell viability was examined by MTT assay. Transfection of miR-146b-5p mimic or inhibitor into HSC-T6 cells was performed, with the aim to identify the influence of miR-146b-5p on HSC-T6 cell behavior. The targeting relationship between miR-146b-5p and HIPK1 was predicted by TargetScan 7.2 and StarBase 3.0 and it was later verified by a dual-luciferase reporter assay. Through lentivirus transfection, the biological function of HIPK1 in regulating the progression of HF and the underlying mechanism were investigated. The results showed that miR-146b-5p was upregulated in liver tissues of rats with HF and activated HSC-T6 cells, while HIPK1 was downregulated in liver tissues of rats with HF and activated HSC-T6 cells. miR-146b-5p was able to upregulate the activation markers of LPS-induced HSC-T6 cells, upregulate COL1A1 and TGF-β, increase cell viability and contribute to fibrosis progression. HIPK1 was validated as the direct target of miR-146b-5p and its overexpression could effectively reduce the effect of miR-146b-5p in contribution to the progression of HF. In conclusion, miR-146b-5p was significantly upregulated during the progression of HF. By targeting and downregulating HIPK1, miR-146b-5p could significantly activate HSCs, upregulate COL1A1 and TGF-β and contribute to fibrosis progression. miR-146b-5p is a potential biomarker and therapeutic target for HF.
format Online
Article
Text
id pubmed-9257962
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher D.A. Spandidos
record_format MEDLINE/PubMed
spelling pubmed-92579622022-07-13 miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1 Xie, Junfeng Cheng, Na Huang, Zhanchao Shu, Xu Xiang, Tianxin Exp Ther Med Articles The present study aimed to explore the biological functions of microRNA (miR)-146b-5p and homeodomain interacting protein kinase 1 (HIPK1) in the progression of hepatic fibrosis (HF) and to identify the underlying mechanism. A rat HF model was established by administering a subcutaneous injection of carbon tetrachloride (CCl(4)). Relative levels of miR-146b-5p and HIPK1 in fibrotic rat liver tissues and the rat hepatic stellate cell (HSC) line HSC-T6 were measured by quantitative reverse transcription PCR, western blotting and immunohistochemistry. Following activation of HSC-T6 cells by lipopolysaccharide (LPS) induction, cell viability was examined by MTT assay. Transfection of miR-146b-5p mimic or inhibitor into HSC-T6 cells was performed, with the aim to identify the influence of miR-146b-5p on HSC-T6 cell behavior. The targeting relationship between miR-146b-5p and HIPK1 was predicted by TargetScan 7.2 and StarBase 3.0 and it was later verified by a dual-luciferase reporter assay. Through lentivirus transfection, the biological function of HIPK1 in regulating the progression of HF and the underlying mechanism were investigated. The results showed that miR-146b-5p was upregulated in liver tissues of rats with HF and activated HSC-T6 cells, while HIPK1 was downregulated in liver tissues of rats with HF and activated HSC-T6 cells. miR-146b-5p was able to upregulate the activation markers of LPS-induced HSC-T6 cells, upregulate COL1A1 and TGF-β, increase cell viability and contribute to fibrosis progression. HIPK1 was validated as the direct target of miR-146b-5p and its overexpression could effectively reduce the effect of miR-146b-5p in contribution to the progression of HF. In conclusion, miR-146b-5p was significantly upregulated during the progression of HF. By targeting and downregulating HIPK1, miR-146b-5p could significantly activate HSCs, upregulate COL1A1 and TGF-β and contribute to fibrosis progression. miR-146b-5p is a potential biomarker and therapeutic target for HF. D.A. Spandidos 2022-06-27 /pmc/articles/PMC9257962/ /pubmed/35837064 http://dx.doi.org/10.3892/etm.2022.11474 Text en Copyright: © Xie 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
Xie, Junfeng
Cheng, Na
Huang, Zhanchao
Shu, Xu
Xiang, Tianxin
miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1
title miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1
title_full miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1
title_fullStr miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1
title_full_unstemmed miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1
title_short miR-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting HIPK1
title_sort mir-146b-5p activation of hepatic stellate cells contributes to the progression of fibrosis by directly targeting hipk1
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9257962/
https://www.ncbi.nlm.nih.gov/pubmed/35837064
http://dx.doi.org/10.3892/etm.2022.11474
work_keys_str_mv AT xiejunfeng mir146b5pactivationofhepaticstellatecellscontributestotheprogressionoffibrosisbydirectlytargetinghipk1
AT chengna mir146b5pactivationofhepaticstellatecellscontributestotheprogressionoffibrosisbydirectlytargetinghipk1
AT huangzhanchao mir146b5pactivationofhepaticstellatecellscontributestotheprogressionoffibrosisbydirectlytargetinghipk1
AT shuxu mir146b5pactivationofhepaticstellatecellscontributestotheprogressionoffibrosisbydirectlytargetinghipk1
AT xiangtianxin mir146b5pactivationofhepaticstellatecellscontributestotheprogressionoffibrosisbydirectlytargetinghipk1