Cargando…
LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b
OBJECTIVE: The exact mechanism and target molecules of liver fibrosis have remained largely elusive. Here, we investigated the role of long noncoding RNA Gm9866(lncRNA-Gm9866) on liver fibrosis. METHODS: The transcription of lncRNA-Gm9866 in activated cells and mouse fibrotic livers was determined b...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621198/ https://www.ncbi.nlm.nih.gov/pubmed/37919785 http://dx.doi.org/10.1186/s12967-023-04642-1 |
_version_ | 1785130365521756160 |
---|---|
author | Liao, Xiaomin Ruan, Xianxian Yao, Peishan Yang, Dan Wu, Xianbin Zhou, Xia Jing, Jie Wei, Dafu Liang, Yaodan Zhang, Taicheng Qin, Shanyu Jiang, Haixing |
author_facet | Liao, Xiaomin Ruan, Xianxian Yao, Peishan Yang, Dan Wu, Xianbin Zhou, Xia Jing, Jie Wei, Dafu Liang, Yaodan Zhang, Taicheng Qin, Shanyu Jiang, Haixing |
author_sort | Liao, Xiaomin |
collection | PubMed |
description | OBJECTIVE: The exact mechanism and target molecules of liver fibrosis have remained largely elusive. Here, we investigated the role of long noncoding RNA Gm9866(lncRNA-Gm9866) on liver fibrosis. METHODS: The transcription of lncRNA-Gm9866 in activated cells and mouse fibrotic livers was determined by quantitative polymerase chain reaction (qRT-PCR). The effects of lentivirus-mediated knockdown or overexpression of lncRNA-Gm9866 in liver fibrosis were examined in vitro and in vivo. Furthermore, bioinformatics analysis, cell samples validation, fluorescence in situ hybridization (FISH) co-localization, RNA binding protein immunoprecipitation (RIP), actinomycin D test and Western blot (WB) were carried out to explore the potential mechanism of lncRNA-Gm9866. RESULTS: The expression of α-smooth muscle actin (α-SMA), Collagen I (COL-1) and lncRNA-Gm9866 were significantly increased in tissues and cells. Overexpressing lncRNA-Gm9866 promoted the activation of hepatic stellate cells (HSCs). Silencing lncRNA-Gm9866 inhibited the activation of HSCs and transforming growth factor-β1 (TGFβ1) induced fibrosis. Overexpressing lncRNA-Gm9866 promoted hepatocytes (HCs) apoptosis and the expression of pro-fibrogenic genes, inhibited the proliferation and migration of HCs. Knockdown of lncRNA-Gm9866 inhibited the apoptosis of HCs, the expression of pro-fibrogenic genes, TGFβ1 induced fibrosis and the occurrence of carbon tetrachloride (CCl4)-induced liver fibrosis, and promoted the proliferation and migration of HCs. Mechanistically, lncRNA-Gm9866 may directly bine with Fam98b. Silencing Fam98b in stably overexpressing lncRNA-Gm9866 cell lines reversed the increase of pro-fibrogenic genes and pro-apoptotic genes, fibrosis related pathway protein TGFβ1, Smad2/3, p-Smad2/3 and Notch3 induced by overexpressing lncRNA-Gm9866. CONCLUSIONS: LncRNA-Gm9866 may regulate TGFβ/Smad and Notch pathways by targeting Fam98b to regulate liver fibrosis. LncRNA-Gm9866 may be a new target for diagnosis and treatment of liver fibrosis. |
format | Online Article Text |
id | pubmed-10621198 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-106211982023-11-03 LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b Liao, Xiaomin Ruan, Xianxian Yao, Peishan Yang, Dan Wu, Xianbin Zhou, Xia Jing, Jie Wei, Dafu Liang, Yaodan Zhang, Taicheng Qin, Shanyu Jiang, Haixing J Transl Med Research OBJECTIVE: The exact mechanism and target molecules of liver fibrosis have remained largely elusive. Here, we investigated the role of long noncoding RNA Gm9866(lncRNA-Gm9866) on liver fibrosis. METHODS: The transcription of lncRNA-Gm9866 in activated cells and mouse fibrotic livers was determined by quantitative polymerase chain reaction (qRT-PCR). The effects of lentivirus-mediated knockdown or overexpression of lncRNA-Gm9866 in liver fibrosis were examined in vitro and in vivo. Furthermore, bioinformatics analysis, cell samples validation, fluorescence in situ hybridization (FISH) co-localization, RNA binding protein immunoprecipitation (RIP), actinomycin D test and Western blot (WB) were carried out to explore the potential mechanism of lncRNA-Gm9866. RESULTS: The expression of α-smooth muscle actin (α-SMA), Collagen I (COL-1) and lncRNA-Gm9866 were significantly increased in tissues and cells. Overexpressing lncRNA-Gm9866 promoted the activation of hepatic stellate cells (HSCs). Silencing lncRNA-Gm9866 inhibited the activation of HSCs and transforming growth factor-β1 (TGFβ1) induced fibrosis. Overexpressing lncRNA-Gm9866 promoted hepatocytes (HCs) apoptosis and the expression of pro-fibrogenic genes, inhibited the proliferation and migration of HCs. Knockdown of lncRNA-Gm9866 inhibited the apoptosis of HCs, the expression of pro-fibrogenic genes, TGFβ1 induced fibrosis and the occurrence of carbon tetrachloride (CCl4)-induced liver fibrosis, and promoted the proliferation and migration of HCs. Mechanistically, lncRNA-Gm9866 may directly bine with Fam98b. Silencing Fam98b in stably overexpressing lncRNA-Gm9866 cell lines reversed the increase of pro-fibrogenic genes and pro-apoptotic genes, fibrosis related pathway protein TGFβ1, Smad2/3, p-Smad2/3 and Notch3 induced by overexpressing lncRNA-Gm9866. CONCLUSIONS: LncRNA-Gm9866 may regulate TGFβ/Smad and Notch pathways by targeting Fam98b to regulate liver fibrosis. LncRNA-Gm9866 may be a new target for diagnosis and treatment of liver fibrosis. BioMed Central 2023-11-02 /pmc/articles/PMC10621198/ /pubmed/37919785 http://dx.doi.org/10.1186/s12967-023-04642-1 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Liao, Xiaomin Ruan, Xianxian Yao, Peishan Yang, Dan Wu, Xianbin Zhou, Xia Jing, Jie Wei, Dafu Liang, Yaodan Zhang, Taicheng Qin, Shanyu Jiang, Haixing LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b |
title | LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b |
title_full | LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b |
title_fullStr | LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b |
title_full_unstemmed | LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b |
title_short | LncRNA-Gm9866 promotes liver fibrosis by activating TGFβ/Smad signaling via targeting Fam98b |
title_sort | lncrna-gm9866 promotes liver fibrosis by activating tgfβ/smad signaling via targeting fam98b |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10621198/ https://www.ncbi.nlm.nih.gov/pubmed/37919785 http://dx.doi.org/10.1186/s12967-023-04642-1 |
work_keys_str_mv | AT liaoxiaomin lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT ruanxianxian lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT yaopeishan lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT yangdan lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT wuxianbin lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT zhouxia lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT jingjie lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT weidafu lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT liangyaodan lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT zhangtaicheng lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT qinshanyu lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b AT jianghaixing lncrnagm9866promotesliverfibrosisbyactivatingtgfbsmadsignalingviatargetingfam98b |