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Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway
PURPOSE: In this study, we aimed to investigate the effect of follistatin (FST) on hepatic steatosis in NAFLD and the underlying mechanism, which has rarely been reported before. METHODS: Liver samples from NAFLD patients and normal liver samples (from liver donors) were collected to investigate hep...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621035/ https://www.ncbi.nlm.nih.gov/pubmed/36325432 http://dx.doi.org/10.2147/DMSO.S380053 |
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author | Tong, Junlu Cong, Li Jia, Yingbin He, Bai-Liang Guo, Yifan He, Jianzhong Li, Decheng Zou, Baojia Li, Jian |
author_facet | Tong, Junlu Cong, Li Jia, Yingbin He, Bai-Liang Guo, Yifan He, Jianzhong Li, Decheng Zou, Baojia Li, Jian |
author_sort | Tong, Junlu |
collection | PubMed |
description | PURPOSE: In this study, we aimed to investigate the effect of follistatin (FST) on hepatic steatosis in NAFLD and the underlying mechanism, which has rarely been reported before. METHODS: Liver samples from NAFLD patients and normal liver samples (from liver donors) were collected to investigate hepatic FST expression in humans. Additionally, human liver cells (LO2) were treated with free fatty acid (FFA) to induce lipid accumulation. Furthermore, lentivirus with FST overexpression or knockdown vectors were used to generate stable cell lines, which were subsequently treated with FFA or FFA and rapamycin. In the animal experiments, male C57BL/6J mice were fed with a high-fat diet (HFD) to induce NAFLD, after which the adeno-associated virus (AAV) gene vectors for FST overexpression were administered. In both cell culture and mice, we evaluated morphological changes and the protein expression of sterol regulatory element-binding protein1 (SREBP1), acetyl-CoA carboxylase1 (ACC1), carbohydrate-responsive element-binding protein (ChREBP), fatty acid synthase (FASN), and Akt/mTOR signaling. The body weight and serum parameters of the mice were also measured. RESULTS: Hepatic FST expression level was higher in NAFLD patients compared to normal samples. In LO2 cells, FST overexpression alleviated lipid accumulation and lipogenesis, whereas FST knockdown aggravated hepatic steatosis. FST could regulate Akt/mTOR signaling, and the mTOR inhibitor rapamycin abolished the effect of FST knockdown on hepatic de novo lipogenesis (DNL). Furthermore, FST expression was increased in HFD mice compared to the corresponding controls. FST overexpression in mice reduced body weight gain, hyperlipidemia, hepatic DNL, and suppressed Akt/mTOR signaling. CONCLUSION: Hepatic FST expression increases in NAFLD and plays a protective role in hepatic steatosis. FST overexpression gene therapy alleviates hepatic steatosis via the mTOR pathway.Therefore, gene therapy for FST is a promising treatment in NAFLD. |
format | Online Article Text |
id | pubmed-9621035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-96210352022-11-01 Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway Tong, Junlu Cong, Li Jia, Yingbin He, Bai-Liang Guo, Yifan He, Jianzhong Li, Decheng Zou, Baojia Li, Jian Diabetes Metab Syndr Obes Original Research PURPOSE: In this study, we aimed to investigate the effect of follistatin (FST) on hepatic steatosis in NAFLD and the underlying mechanism, which has rarely been reported before. METHODS: Liver samples from NAFLD patients and normal liver samples (from liver donors) were collected to investigate hepatic FST expression in humans. Additionally, human liver cells (LO2) were treated with free fatty acid (FFA) to induce lipid accumulation. Furthermore, lentivirus with FST overexpression or knockdown vectors were used to generate stable cell lines, which were subsequently treated with FFA or FFA and rapamycin. In the animal experiments, male C57BL/6J mice were fed with a high-fat diet (HFD) to induce NAFLD, after which the adeno-associated virus (AAV) gene vectors for FST overexpression were administered. In both cell culture and mice, we evaluated morphological changes and the protein expression of sterol regulatory element-binding protein1 (SREBP1), acetyl-CoA carboxylase1 (ACC1), carbohydrate-responsive element-binding protein (ChREBP), fatty acid synthase (FASN), and Akt/mTOR signaling. The body weight and serum parameters of the mice were also measured. RESULTS: Hepatic FST expression level was higher in NAFLD patients compared to normal samples. In LO2 cells, FST overexpression alleviated lipid accumulation and lipogenesis, whereas FST knockdown aggravated hepatic steatosis. FST could regulate Akt/mTOR signaling, and the mTOR inhibitor rapamycin abolished the effect of FST knockdown on hepatic de novo lipogenesis (DNL). Furthermore, FST expression was increased in HFD mice compared to the corresponding controls. FST overexpression in mice reduced body weight gain, hyperlipidemia, hepatic DNL, and suppressed Akt/mTOR signaling. CONCLUSION: Hepatic FST expression increases in NAFLD and plays a protective role in hepatic steatosis. FST overexpression gene therapy alleviates hepatic steatosis via the mTOR pathway.Therefore, gene therapy for FST is a promising treatment in NAFLD. Dove 2022-10-27 /pmc/articles/PMC9621035/ /pubmed/36325432 http://dx.doi.org/10.2147/DMSO.S380053 Text en © 2022 Tong et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Tong, Junlu Cong, Li Jia, Yingbin He, Bai-Liang Guo, Yifan He, Jianzhong Li, Decheng Zou, Baojia Li, Jian Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway |
title | Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway |
title_full | Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway |
title_fullStr | Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway |
title_full_unstemmed | Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway |
title_short | Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway |
title_sort | follistatin alleviates hepatic steatosis in nafld via the mtor dependent pathway |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9621035/ https://www.ncbi.nlm.nih.gov/pubmed/36325432 http://dx.doi.org/10.2147/DMSO.S380053 |
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