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A9.6 Effect of mPGES-1 targeting on lipid metabolism in human cells
  1. Helena Idborg1,
  2. Joan Raouf1,
  3. Elena Ossipova1,
  4. Antonio Checa2,
  5. Petter Olsson3,
  6. Patrick Leclerc1,
  7. Ganna Oliynik1,
  8. Craig Wheelock2,
  9. Per-Johan Jakobsson1,
  10. Marina Korotkova1
  1. 1Rheumatology Unit, Department of Medicine, Karolinska Institutet, Sweden
  2. 2Department of Medical Biochemistry and Biophysics, Bioanalytical Chemistry Research Laboratory in Inflammatory Metabolomics, Karolinska Institutet, Sweden
  3. 3Department of Analytical Chemistry, Stockholm University, Sweden


Background Microsomal prostaglandin E synthase-1 (mPGES-1) is the terminal enzyme in the induced PGE2 production and well-recognised target for the development of novel anti-inflammatory drugs. Genetic deletion and inhibition of mPGES-1 appears to be protective in experimental models of arthritis. Targeting mPGES-1 alters eicosanoid profiles and may potentially affect the metabolism of other lipids. Fatty acids (FA) play essential roles as energy substrates, membrane structural components, second messengers and precursors of lipid mediators. Genetic deletion of mPGES-1 resulted in reduced levels of MUFA in the spleen suggesting a decreased activity/expression of stearoyl-CoA-desaturase (SCD). SCD has been implicated in modulation of inflammation. However whether mPGES-1 inhibition affects lipid metabolism in human cells is not known.

Objective To investigate the effect of mPGES-1 deletion/inhibition on lipid metabolism in human cells.

Methods  A549 cells were induced with IL-1b and treated with mPGES-1 inhibitor (compound III) or COX-2 inhibitor (NS398). Eicosanoid profiles were analysed using LC-MS/MS and protein profiles were analysed using mass spectrometry based proteomics. FA composition of total lipids was determined using gas chromatography with flame ionization detector and sphingolipids were analysed by LC-MS/MS.

Results Proteomic analysis of A549 cells identified the reduction of SCD levels in response to treatment with mPGES-1 or COX-2 inhibitors, as well as the suppression of the levels of a number of proteins involved in metabolism of fatty acids and sphingolipids.

Conclusion Data reveals that down-regulation of COX-2/mPGES-1/ PGE2 axis affects the lipid metabolism in A549 cells. These effects have important implications regarding potential consequences of pharmacologic mPGES-1 inhibition.

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