Follistatin Alleviates Hepatic Steatosis in NAFLD via the mTOR Dependent Pathway

被引:11
作者
Tong, Junlu [1 ,2 ]
Cong, Li [1 ]
Jia, Yingbin [3 ]
He, Bai-Liang [4 ]
Guo, Yifan [1 ]
He, Jianzhong [5 ]
Li, Decheng [3 ]
Zou, Baojia [2 ,3 ]
Li, Jian [2 ,3 ]
机构
[1] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Endocrinol, Zhuhai, Peoples R China
[2] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Cent Lab, Zhuhai, Peoples R China
[3] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Hepatobiliary Surg, Zhuhai, Peoples R China
[4] Sun Yat Sen Univ, Affiliated Hosp 5, Guangdong Prov Engn Res Ctr Mol Imaging, Guangdong Prov Key Lab Biomed Imaging, Zhuhai, Peoples R China
[5] Sun Yat Sen Univ, Affiliated Hosp 5, Dept Pathol, Zhuhai, Peoples R China
来源
DIABETES METABOLIC SYNDROME AND OBESITY | 2022年 / 15卷
基金
中国国家自然科学基金;
关键词
follistatin; non-alcoholic fatty liver disease; free fatty acid; lipid synthesis; DE-NOVO LIPOGENESIS; FATTY LIVER-DISEASE; CIRCULATING FOLLISTATIN; INSULIN-RESISTANCE; ACTIVIN-A;
D O I
10.2147/DMSO.S380053
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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 subse-quently 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.
引用
收藏
页码:3285 / 3301
页数:17
相关论文
共 49 条
[1]   Follistatin promotes adipocyte differentiation, browning, and energy metabolism [J].
Braga, Melissa ;
Reddy, Srinivasa T. ;
Vergnes, Laurent ;
Pervin, Shehla ;
Grijalva, Victor ;
Stout, David ;
David, John ;
Li, Xinmin ;
Tomasian, Venina ;
Reid, Christopher B. ;
Norris, Keith C. ;
Devaskar, Sherin U. ;
Reue, Karen ;
Singh, Rajan .
JOURNAL OF LIPID RESEARCH, 2014, 55 (03) :375-384
[2]   Insulin resistance in non-diabetic patients with non-alcoholic fatty liver disease: sites and mechanisms [J].
Bugianesi, E ;
Gastaldelli, A ;
Vanni, E ;
Gambino, R ;
Cassader, M ;
Baldi, S ;
Ponti, V ;
Pagano, G ;
Ferrannini, E ;
Rizzetto, M .
DIABETOLOGIA, 2005, 48 (04) :634-642
[3]   NAFLD: A multisystem disease [J].
Byrne, Christopher D. ;
Targher, Giovanni .
JOURNAL OF HEPATOLOGY, 2015, 62 :S47-S64
[4]   The Roles of mTOR Complexes in Lipid Metabolism [J].
Caron, Alexandre ;
Richard, Denis ;
Laplante, Mathieu .
ANNUAL REVIEW OF NUTRITION, VOL 35, 2015, 35 :321-348
[5]   Combination therapy for non-alcoholic steatohepatitis: rationale, opportunities and challenges [J].
Dufour, Jean-Francois ;
Caussy, Cyrielle ;
Loomba, Rohit .
GUT, 2020, 69 (10) :1877-1884
[6]   A new definition for metabolic dysfunction-associated fatty liver disease: An international expert consensus statement [J].
Eslam, Mohammed ;
Newsome, Philip N. ;
Sarin, Shiv K. ;
Anstee, Quentin M. ;
Targher, Giovanni ;
Romero-Gomez, Manuel ;
Zelber-Sagi, Shira ;
Wong, Vincent Wai-Sun ;
Dufour, Jean-Francois ;
Schattenberg, Joern M. ;
Kawaguchi, Takumi ;
Arrese, Marco ;
Valenti, Luca ;
Shiha, Gamal ;
Tiribelli, Claudio ;
Yki-Jarvinen, Hannele ;
Fan, Jian-Gao ;
Gronbaek, Henning ;
Yilmaz, Yusuf ;
Cortez-Pinto, Helena ;
Oliveira, Claudia P. ;
Bedossa, Pierre ;
Adams, Leon A. ;
Zheng, Ming-Hua ;
Fouad, Yasser ;
Chan, Wah-Kheong ;
Mendez-Sanchez, Nahum ;
Ahn, Sang Hoon ;
Castera, Laurent ;
Bugianesi, Elisabetta ;
Ratziu, Vlad ;
George, Jacob .
JOURNAL OF HEPATOLOGY, 2020, 73 (01) :202-209
[7]   Mechanisms of NAFLD development and therapeutic strategies [J].
Friedman, Scott L. ;
Neuschwander-Tetri, Brent A. ;
Rinella, Mary ;
Sanyal, Arun J. .
NATURE MEDICINE, 2018, 24 (07) :908-922
[8]   Plasma follistatin is elevated in patients with type 2 diabetes: relationship to hyperglycemia, hyperinsulinemia, and systemic low-grade inflammation [J].
Hansen, J. ;
Rinnov, A. ;
Krogh-Madsen, R. ;
Fischer, C. P. ;
Andreasen, A. S. ;
Berg, R. M. G. ;
Moller, K. ;
Pedersen, B. K. ;
Plomgaard, P. .
DIABETES-METABOLISM RESEARCH AND REVIEWS, 2013, 29 (06) :463-472
[9]   Exercise Induces a Marked Increase in Plasma Follistatin: Evidence That Follistatin Is a Contraction-Induced Hepatokine [J].
Hansen, Jakob ;
Brandt, Claus ;
Nielsen, Anders R. ;
Hojman, Pernille ;
Whitham, Martin ;
Febbraio, Mark A. ;
Pedersen, Bente K. ;
Plomgaard, Peter .
ENDOCRINOLOGY, 2011, 152 (01) :164-171
[10]   Circulating follistatin in relation to energy metabolism [J].
Hansen, Jakob Schioler ;
Plomgaard, Peter .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2016, 433 (0C) :87-93