Regulation of hepatic fatty acid elongase and desaturase expression in diabetes and obesity

• Published in: Journal of lipid research Vol. 47; no. 9; pp. 2028 - 2041
• Main Authors: Wang, Yun, Botolin, Daniela, Xu, Jinghua, Christian, Barbara, Mitchell, Ernestine, Jayaprakasam, Bolleddula, Nair, Muraleedharan, Peters, Jeffery M., Busik, Julia, Olson, L. Karl, Jump, Donald B.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.09.2006; American Society for Biochemistry and Molecular Biology; Elsevier
• Subjects: Acetyltransferases - genetics; Acetyltransferases - metabolism; Adult; Animals; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - genetics; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors - metabolism; carbohydrate-regulatory element binding protein; Diabetes Mellitus - genetics; Diabetes Mellitus - metabolism; Diabetes Mellitus - pathology; Fatty Acid Desaturases - genetics; Fatty Acid Desaturases - metabolism; Fatty Acid Elongases; Female; Glucose - pharmacology; Humans; Hydrocarbons, Fluorinated; Insulin - pharmacology; Leptin - deficiency; Leptin - genetics; lipid metabolism; liver; Liver - cytology; Liver - drug effects; Liver - metabolism; liver X receptor; Male; MAX-like factor X; Mice; Mice, Inbred C57BL; Mice, Obese; Middle Aged; Obesity - chemically induced; Obesity - genetics; Obesity - metabolism; peroxisome proliferator-activated receptor; peroxisome proliferator-activated receptor α; PPAR alpha - antagonists & inhibitors; PPAR alpha - metabolism; Pyrimidines - pharmacology; Rats; Rats, Sprague-Dawley; receptors; Sterol Regulatory Element Binding Protein 1 - genetics; Sterol Regulatory Element Binding Protein 1 - metabolism; sterol-regulatory element binding protein; sterol-regulatory element binding protein-1; Sulfonamides - pharmacology; MAX-like factor X; carbohydrate-regulatory element binding protein; liver X receptor; sterol-regulatory element binding protein-1; peroxisome proliferator-activated receptor α
• ISSN: 0022-2275; 1539-7262
• DOI: 10.1194/jlr.M600177-JLR200

Fatty acid elongases and desaturases play an important role in hepatic and whole body lipid composition. We examined the role that key transcription factors played in the control of hepatic elongase and desaturase expression. Studies with peroxisome proliferator-activated receptor α (PPARα)-deficient mice establish that PPARα was required for WY14643-mediated induction of fatty acid elongase-5 (Elovl-5), Elovl-6, and all three desaturases [Δ5 desaturase (Δ5D), Δ6D, and Δ9D]. Increased nuclear sterol-regulatory element binding protein-1 (SREBP-1) correlated with enhanced expression of Elovl-6, Δ5D, Δ6D, and Δ9D. Only Δ9D was also regulated independently by liver X receptor (LXR) agonist. Glucose induction of l-type pyruvate kinase, Δ9D, and Elovl-6 expression required the carbohydrate-regulatory element binding protein/MAX-like factor X (ChREBP/MLX) heterodimer. Suppression of Elovl-6 and Δ9D expression in livers of streptozotocin-induced diabetic rats and high fat-fed glucose-intolerant mice correlated with low levels of nuclear SREBP-1. In leptin-deficient obese mice (Lepob/ob), increased SREBP-1 and MLX nuclear content correlated with the induction of Elovl-5, Elovl-6, and Δ9D expression and the massive accumulation of monounsaturated fatty acids (18:1,n-7 and 18:1,n-9) in neutral lipids. Diabetes- and obesity-induced changes in hepatic lipid composition correlated with changes in elongase and desaturase expression. In conclusion, these studies establish a role for PPARα, LXR, SREBP-1, ChREBP, and MLX in the control of hepatic fatty acid elongase and desaturase expression and lipid composition.