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The antileukemic agent asparaginase triggers the amino acid response (AAR) in the liver by activating the eukaryotic initiation factor 2 (eIF2) kinase general control nonderepressible 2 (GCN2). To explore the mechanism by which AAR induction is necessary to mitigate hepatic lipid accumulation and prevent liver dysfunction during continued asparaginase treatment, wild-type and Gcn2 null mice were injected once daily with asparaginase or phosphate buffered saline for up to 14 days. Asparaginase induced mRNA expression of multiple AAR genes and greatly increased circulating concentrations of the metabolic hormone fibroblast growth factor 21 (FGF21) independent of food intake. Loss of Gcn2 precluded mRNA expression and circulating levels of FGF21 and blocked mRNA expression of multiple genes regulating lipid synthesis and metabolism including Fas, Ppara, Pparg, Acadm, and Scd1 in both liver and white adipose tissue. Furthermore, rates of triglyceride export and protein expression of apolipoproteinB-100 were significantly reduced in the livers of Gcn2 null mice treated with asparaginase, providing a mechanistic basis for the increase in hepatic lipid content. Loss of AAR-regulated antioxidant defenses in Gcn2 null livers was signified by reduced Gpx1 gene expression alongside increased lipid peroxidation. Substantial reductions in antithrombin III hepatic expression and activity in the blood of asparaginase-treated Gcn2 null mice indicated liver dysfunction. These results suggest that the ability of the liver to adapt to prolonged asparaginase treatment is influenced by GCN2-directed regulation of FGF21 and oxidative defenses, which, when lost, corresponds with maladaptive effects on lipid metabolism and hemostasis.

Original publication

DOI

10.1152/ajpendo.00361.2014

Type

Journal article

Journal

Am J Physiol Endocrinol Metab

Publication Date

15/02/2015

Volume

308

Pages

E283 - E293

Keywords

adipose, amino acid response, antithrombin III, apolipoprotein B-100, eukaryotic initiation factor 2, fibroblast growth factor 21, general control nonderepressible 2, liver, mice, oxidative stress, steatosis, Adipose Tissue, White, Animals, Antineoplastic Agents, Asparaginase, Biomarkers, Chemical and Drug Induced Liver Injury, Escherichia coli Proteins, Female, Fibroblast Growth Factors, Gene Expression Regulation, Homeostasis, Injections, Intraperitoneal, Lipid Peroxidation, Liver, Male, Mice, Inbred C57BL, Mice, Knockout, Protein-Serine-Threonine Kinases, RNA, Messenger, Triglycerides