An integrative approach to assessing effects of a short-term Western diet on gene expression in rat liver

被引:1
作者
Welles, Jaclyn E. [1 ]
Lacko, Holly [1 ]
Kawasawa, Yuka Imamura [2 ]
Dennis, Michael D. [1 ]
Jefferson, Leonard S. [1 ]
Kimball, Scot R. [1 ]
机构
[1] Penn State Coll Med, Dept Cellular & Mol Physiol, Hershey, PA 17033 USA
[2] Penn State Coll Med, Dept Pharmacol, Hershey, PA USA
来源
FRONTIERS IN ENDOCRINOLOGY | 2022年 / 13卷
关键词
diet-induced obesity; nonalcoholic fatty liver disease (NAFLD); mRNA translation; mTORC1; gene regulation; liver; metabolism; DE-NOVO LIPOGENESIS; RAPAMYCIN COMPLEX 1; MAMMALIAN TARGET; MESSENGER-RNA; INSULIN-RESISTANCE; TRANSLATIONAL REGULATION; INDUCED OBESITY; ACTIVATION; MTORC1; PATHWAY;
D O I
10.3389/fendo.2022.1032293
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Consumption of a diet rich in saturated fatty acids and carbohydrates contributes to the accumulation of fat in the liver and development of non-alcoholic steatohepatitis (NASH). Herein we investigated the hypothesis that short-term consumption of a high fat/sucrose Western diet (WD) alters the genomic and translatomic profile of the liver in association with changes in signaling through the protein kinase mTORC1, and that such alterations contribute to development of NAFLD. The results identify a plethora of mRNAs that exhibit altered expression and/or translation in the liver of rats consuming a WD compared to a CD. In particular, consumption of a WD altered the abundance and ribosome association of mRNAs involved in lipid and fatty acid metabolism, as well as those involved in glucose metabolism and insulin signaling. Hepatic mTORC1 signaling was enhanced when rats were fasted overnight and then refed in the morning; however, this effect was blunted in rats fed a WD as compared to a CD. Despite similar plasma insulin concentrations, fatty acid content was elevated in the liver of rats fed a WD as compared to a CD. We found that feeding had a significant positive effect on ribosome occupancy of 49 mRNAs associated with hepatic steatosis (e.g., LIPE, LPL), but this effect was blunted in the liver of rats fed a WD. In many cases, changes in ribosome association were independent of alterations in mRNA abundance, suggesting a critical role for diet-induced changes in mRNA translation in the expression of proteins encoded by those mRNAs. Overall, the findings demonstrate that short-term consumption of a WD impacts hepatic gene expression by altering the abundance of many mRNAs, but also causes wide-spread variation in mRNA translation that potentially contribute to development of hepatic steatosis.
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页数:14
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共 82 条
  • [1] Non-alcoholic fatty liver disease: The diagnosis and management
    Abd El-Kader, Shehab M.
    El-Den Ashmawy, Eman M. Salah
    [J]. WORLD JOURNAL OF HEPATOLOGY, 2015, 7 (06) : 846 - 858
  • [2] Too Little mTORC1 Activity Injures the Liver
    Abraham, Robert T.
    [J]. CELL METABOLISM, 2014, 20 (01) : 4 - 6
  • [3] The regulation of hepatic protein synthesis during fasting in the rat
    Anand, P
    Gruppuso, PA
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (16) : 16427 - 16436
  • [4] Deficiency of dietary EAA preferentially inhibits mRNA translation of ribosomal proteins in liver of meal-fed rats
    Anthony, TG
    Reiter, AK
    Anthony, JC
    Kimball, SR
    Jefferson, LS
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 281 (03): : E430 - E439
  • [5] Fructose supplementation impairs rat liver autophagy through mTORC activation without inducing endoplasmic reticulum stress
    Baena, Miguel
    Sangueesa, Gemma
    Hutter, Natalia
    Sanchez, Rosa M.
    Roglans, Nuria
    Laguna, Juan C.
    Alegret, Marta
    [J]. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2015, 1851 (02): : 107 - 116
  • [6] Characterization of the Murine SIRT3 Mitochondrial Localization Sequence and Comparison of Mitochondrial Enrichment and Deacetylase Activity of Long and Short SIRT3 Isoforms
    Bao, Jianjun
    Lu, Zhongping
    Joseph, Joshua J.
    Carabenciov, Darin
    Dimond, Christopher C.
    Pang, Liyan
    Samsel, Leigh
    Mccoy, J. Philip, Jr.
    Leclerc, Jaime
    Nguyen, PhuongMai
    Gius, David
    Sack, Michael N.
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 2010, 110 (01) : 238 - 247
  • [7] RETRACTED: Hepatic Glucagon Action Is Essential for Exercise-Induced Reversal of Mouse Fatty Liver (Retracted article. See vol. 65, pg. 2463, 2016)
    Berglund, Eric D.
    Lustig, Daniel G.
    Baheza, Richard A.
    Hasenour, Clinton M.
    Lee-Young, Robert S.
    Donahue, E. Patrick
    Lynes, Sara E.
    Swift, Larry L.
    Charron, Maureen J.
    Damon, Bruce M.
    Wasserman, David H.
    [J]. DIABETES, 2011, 60 (11) : 2720 - 2729
  • [8] The mammalian target of rapamycin regulates lipid metabolism in primary cultures of rat hepatocytes
    Brown, Nicholas F.
    Stefanovic-Racic, Maja
    Sipula, Ian J.
    Perdomo, German
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 2007, 56 (11): : 1500 - 1507
  • [9] mRNAs, proteins and the emerging principles of gene expression control
    Buccitelli, Christopher
    Selbach, Matthias
    [J]. NATURE REVIEWS GENETICS, 2020, 21 (10) : 630 - 644
  • [10] Mammalian Target of Rapamycin Complex 1 Suppresses Lipolysis, Stimulates Lipogenesis, and Promotes Fat Storage
    Chakrabarti, Partha
    English, Taylor
    Shi, Jun
    Smas, Cynthia M.
    Kandror, Konstantin V.
    [J]. DIABETES, 2010, 59 (04) : 775 - 781