4.7 Article

Obesity resistance and deregulation of lipogenesis in Δ6-fatty acid desaturase (FADS2) deficiency

Journal

EMBO REPORTS
Volume 15, Issue 1, Pages 110-120

Publisher

WILEY
DOI: 10.1002/embr.201338041

Keywords

AA- and DHA-fads2(-/-) mouse mutants; abnormal DAG-structures of PL; deregulated lipogenesis; FADS2-deficiency; hepatic steatosis

Funding

  1. Center of Molecular Medicine, University of Cologne
  2. CECAD (Cluster of Excellence, Cellular Stress Response in Aging Related Diseases), University of Cologne
  3. Fritz-Thyssen-Stiftung

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Delta-6-fatty acid desaturase (FADS2) is the key enzyme in the biosynthesis of polyunsaturated fatty acids (PUFAs), the essential structural determinants of mammalian membrane lipid-bilayers. We developed the auxotrophic fads2(-/-) mouse mutant to assess the enigmatic role of omega 3- and omega 6-PUFAs in lipid homeostasis, membrane structure and function. Obesity resistance is another major phenotype of the fads2(-/-) mutant, the molecular basis of which is unknown. Phospholipidomic profiling of membrane systems of fads2(-/-) mice revealed diacylglycerol-structures, deprived of PUFAs but substituted with surrogate eicosa-5,11,14-trienoic acid. omega 6-Arachidonic (AA) and omega 3-docosahexaenoic acid (DHA) supplemented diets transformed fads2(-/-) into AA-fads2(-/-) and DHA-fads2(-/-) mutants. Severely altered phospholipid-bilayer structures of subcellular membranes of fads2(-/-) liver specifically interfered with maturation of transcription factor sterol-regulatory-element-binding protein, the key regulator of lipogenesis and lipid homeostasis. This study strengthens the concept that specific PUFA-substituted membrane phospholipid species are critical constituents of the structural platform operative in lipid homeostasis in normal and disease conditions.

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