Evolution of hepatic steatosis to fibrosis and adenoma formation in liver-specific growth hormone receptor knockout mice

被引:41
|
作者
Fan, Yong [1 ,2 ]
Fang, Xin [1 ,3 ]
Tajima, Asako [1 ,2 ]
Geng, Xuehui [2 ]
Ranganathan, Sarangarajan [4 ]
Dong, Henry [2 ]
Trucco, Massimo [1 ,2 ]
Sperling, Mark A. [5 ]
机构
[1] Allegheny Hlth Network, Inst Cellular Therapeut, 11th Floor,South Tower,320 E North Ave, Pittsburgh, PA 15212 USA
[2] Univ Pittsburgh, Sch Med, Dept Pediat, Div Immunogenet, Pittsburgh, PA 15261 USA
[3] Fujian Med Univ, Union Hosp, Dept Pediat, Fuzhou, Peoples R China
[4] UPMC, Childrens Hosp Pittsburgh, Dept Pathol, Pittsburgh, PA USA
[5] Univ Pittsburgh, Sch Med, Dept Pediat, Div Endocrinol, Pittsburgh, PA 15261 USA
来源
关键词
growth hormone receptor; hepatic steatosis; hepatocellular adenoma; NAFLD;
D O I
10.3389/fendo.2014.00218
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Non-alcoholic fatty liver disease (NAFLD) is one of the most common forms of chronic liver diseases closely associated with obesity and insulin resistance; deficient growth hormone (GH) action in liver has been implicated as a mechanism. Here, we investigated the evolution of NAFLD in aged mice with liver-specific GHR deletion. Methods: We examined glucose tolerance, insulin responsiveness, and lipid profiles in aged male mice (44-50 weeks) with GHRLD. We performed proteomics analysis, pathway based Superarray assay, as well as quantitative RT-PCR to gain molecular insight into the mechanism(s) of GHR-deficiency-mediated NAFLD. In addition, we examined the pathological changes of livers of aged GHRLD male mice. Results: The biochemical profile was consistent with that of the metabolic syndrome: abnormal glucose tolerance, impaired insulin secretion, and hyperlipidemia. RT-qPCR analysis of key markers of inflammation revealed a three- to fivefold increase in TNF alpha and CCL3, confirming the presence of inflammation. Expression of fibrotic markers (e.g., CoI1A2 and Col3A1) was significantly increased, together with a two- to threefold increase in TGF1 transcripts. Proteomics analyses showed a marked decrease of Mup1 and Selenbp2. In addition, pathway-analysis showed that the expression of cell cycle and growth relevant genes (i.e., Ccndl, Socs2, Socs3, and Egfr) were markedly affected in GHRLD liver. Microscopic analyses (H&E) of GHRLD livers revealed the presence of hepatic adenomas of different stages of malignancy. Conclusion: Abrogation of GH signaling in male liver leads to metabolic syndrome, hepatic steatosis, increased inflammation and fibrosis, and development of hepatic tumor. Since obesity, a common precursor of NAFLD, is a state of deficient GH secretion and action, the GHRLD model could be used to unravel the contribution of compromised hepatic GH signaling in these pathological processes, and help to identify potential targets for intervention.
引用
收藏
页数:10
相关论文
共 50 条
  • [41] Expression of Apoptosis-Related Genes in Liver-Specific Growth Hormone Receptor Gene-Disrupted Mice Is Sex Dependent
    Gesing, Adam
    Wang, Feiya
    List, Edward O.
    Berryman, Darlene E.
    Masternak, Michal M.
    Lewinski, Andrzej
    Karbownik-Lewinska, Malgorzata
    Kopchick, John J.
    Bartke, Andrzej
    JOURNALS OF GERONTOLOGY SERIES A-BIOLOGICAL SCIENCES AND MEDICAL SCIENCES, 2015, 70 (01): : 44 - 52
  • [42] Compensatory alterations of insulin signal transduction in liver of growth hormone receptor knockout mice
    Dominici, FP
    Diaz, GA
    Bartke, A
    Kopchick, JJ
    Turyn, D
    JOURNAL OF ENDOCRINOLOGY, 2000, 166 (03) : 579 - 590
  • [43] Impaired lipid metabolism in liver-specific phosphoenolpyruvate carboxykinase (PEPCK) knockout mice
    She, PX
    Shelton, KD
    Magnuson, MA
    DIABETES, 2000, 49 : A6 - A6
  • [44] Effects of rapamycin on growth hormone receptor knockout mice
    Fang, Yimin
    Hill, Cristal M.
    Darcy, Justin
    Reyes-Ordonez, Adriana
    Arauz, Edwin
    McFadden, Samuel
    Zhang, Chi
    Osland, Jared
    Gao, John
    Zhang, Tian
    Frank, Stuart J.
    Javors, Martin A.
    Yuan, Rong
    Kopchick, John J.
    Sun, Liou Y.
    Chen, Jie
    Bartke, Andrzej
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2018, 115 (07) : E1495 - E1503
  • [45] A Lipid Nanoparticle-Based Method for the Generation of Liver-Specific Knockout Mice
    Morita, Sumiyo
    Horii, Takuro
    Kimura, Mika
    Kobayashi, Ryosuke
    Tanaka, Hiroki
    Akita, Hidetaka
    Hatada, Izuho
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2023, 24 (18)
  • [46] DEFECTIVE FASTED-FED TRANSITION IN LIVER-SPECIFIC β-CATENIN KNOCKOUT MICE
    Yeh, Tzu-Hsuan
    Krauland, Lindsay K.
    Liu, Shiguang
    Stefanovic-Racic, Maja
    Shiva, Sruti
    Ritov, Vladimir B.
    Menchikova, Elizaveta V.
    Alonso, Laura C.
    Behari, Jaideep
    HEPATOLOGY, 2010, 52 (04) : 602A - 602A
  • [47] Stability and reproducibility assessment of liver-specific GK gene knockout mice and the role of hepatic GK in the pathogenesis of diabetes mellitus
    Mao, Yiqing
    Xiao, Meifang
    Zhang, Yali
    Zhang, Xuemei
    Zhao, Shuyong
    Li, Hui
    Niu, Gang
    Tan, Huanran
    ACTA PHARMACOLOGICA SINICA, 2006, 27 : 302 - 302
  • [48] Generation and characterisation of liver-specific Jagged2 knockout mice for liver cancer research
    Nguyen, Romario
    Bae, Sarah
    Qiao, Liang
    George, Jacob
    ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2021, 17 : 50 - 50
  • [49] Short Term Feeding of a High Fat Diet Exerts an Additive Effect on Hepatocellular Damage and Steatosis in Liver-Specific PTEN Knockout Mice
    Shearn, Colin T.
    Mercer, Kelly E.
    Orlicky, David J.
    Hennings, Leah
    Smathers-McCullough, Rebecca L.
    Stiles, Bangyan L.
    Ronis, Martin J. J.
    Petersen, Dennis R.
    PLOS ONE, 2014, 9 (05):
  • [50] Liver-specific deletion of TSHR inhibits hepatic lipid accumulation in mice
    Zhou, Lingyan
    Wu, Kunpeng
    Zhang, Liya
    Gao, Ling
    Chen, Shihong
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2018, 497 (01) : 39 - 45