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Deletion of ELOVL5 leads to fatty liver through activation of SREBP-1c in mice.

Journal of lipid research | Mar 17, 2009

Elongation of very long chain fatty acids (ELOVL)5 is one of seven mammalian fatty acid condensing enzymes involved in microsomal fatty acid elongation. To determine the in vivo substrates and function of ELOVL5, we generated Elovl5(-/-) mice. Studies using liver microsomal protein from wild-type and knockout mice demonstrated that the elongation of gamma-linolenic (C18:3, n-6) to dihomo-gamma-linolenic (C20:3, n-6) and stearidonic (C18:4, n-3) to omega3-arachidonic acid (C20:4, n-3) required ELOVL5 activity. Tissues of Elovl5(-/-) mice accumulated the C18 substrates of ELOVL5 and the levels of the downstream products, arachidonic acid (C20:4, n-6) and docosahexaenoic acid (DHA, C22:6, n-3), were decreased. A consequence of decreased cellular arachidonic acid and DHA concentrations was the activation of sterol regulatory element-binding protein (SREBP)-1c and its target genes involved in fatty acid and triglyceride synthesis, which culminated in the development of hepatic steatosis in Elovl5(-/-) mice. The molecular and metabolic changes in fatty acid metabolism in Elovl5(-/-) mice were reversed by dietary supplementation with arachidonic acid and DHA. These studies demonstrate that reduced ELOVL5 activity leads to hepatic steatosis, and endogenously synthesized PUFAs are key regulators of SREBP-1c activation and fatty acid synthesis in livers of mice.

Pubmed ID: 18838740 RIS Download

Mesh terms: Acetyltransferases | Animals | Base Sequence | Cells, Cultured | Cholesterol | DNA Probes | Fatty Acids | Fatty Liver | Female | Hepatocytes | Liver | Male | Mice | Mice, Inbred C57BL | Mice, Knockout | Models, Biological | RNA, Messenger | Sterol Regulatory Element Binding Protein 1

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Associated grants

  • Agency: NIDDK NIH HHS, Id: PL1 DK081182
  • Agency: NHLBI NIH HHS, Id: R01 HL038049
  • Agency: NIDDK NIH HHS, Id: DK-081182
  • Agency: NHLBI NIH HHS, Id: HL-38049

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