Double bonds of unsaturated fatty acids differentially regulate mitochondrial cardiolipin remodeling

Lipids Health Dis. 2019 Feb 14;18(1):53. doi: 10.1186/s12944-019-0990-y.

Abstract

Background: Supplemented fatty acids can incorporate into cardiolipin (CL) and affect its remodeling. The change in CL species may alter the mitochondrial membrane composition, potentially disturbing the mitochondrial structure and function during inflammation.

Method: To investigate the effect of the unsaturation of fatty acids on CL, we supplemented macrophage-like RAW264.7 cells with 18-carbon unsaturated fatty acids including oleic acid (OA, 18:1), linoleic acid (LA, 18:2), α-linolenic acid (ALA, 18:3), γ-linolenic acid (GLA, 18:3), and stearidonic acid (SDA, 18:4). Mitochondrial changes in CL were measured through mass spectrometry.

Result: Our data indicated that OA(18:1) was the most efficient fatty acid that incorporated into CL, forming symmetrical CL without fatty acid elongation and desaturation. In addition, LA(18:2) and ALA(18:3) were further elongated before incorporation, significantly increasing the number of double bonds and the chain length of CL. GLA and SDA were not optimal substrates for remodeling enzymes. The findings of RT-qPCR experiments revealed that none of these changes in CL occurred through the regulation of CL remodeling- or synthesis-related genes. The fatty acid desaturase and transportation genes-Fads2 and Cpt1a, respectively-were differentially regulated by the supplementation of five unsaturated 18-carbon fatty acids.

Conclusions: The process of fatty acid incorporation to CL was regulated by the fatty acid desaturation and transportation into mitochondria in macrophage. The double bonds of fatty acids significantly affect the incorporation process and preference. Intact OA(18:1) was incorporated to CL; LA(18:2) and ALA(18:3) were desaturated and elongated to long chain fatty acid before the incorporation; GLA(18:3) and SDA(18:4) were unfavorable for the CL incorporation.

Keywords: 18-carbon unsaturated fatty acids; Cardiolipin; Mass spectrometry; Mitochondrial membrane composition.

MeSH terms

  • Animals
  • Biological Transport
  • Cardiolipins / biosynthesis*
  • Carnitine O-Palmitoyltransferase / genetics
  • Carnitine O-Palmitoyltransferase / metabolism
  • Fatty Acid Desaturases / genetics
  • Fatty Acid Desaturases / metabolism
  • Fatty Acids, Omega-3 / chemistry
  • Fatty Acids, Omega-3 / metabolism
  • Fatty Acids, Omega-3 / pharmacology*
  • Gene Expression Profiling
  • Gene Expression Regulation
  • Linoleic Acid / chemistry
  • Linoleic Acid / metabolism
  • Linoleic Acid / pharmacology*
  • Mice
  • Mitochondria / chemistry
  • Mitochondria / drug effects
  • Mitochondria / metabolism
  • Mitochondrial Membranes / chemistry
  • Mitochondrial Membranes / drug effects*
  • Mitochondrial Membranes / metabolism
  • Oleic Acid / chemistry
  • Oleic Acid / metabolism
  • Oleic Acid / pharmacology*
  • RAW 264.7 Cells
  • Structure-Activity Relationship
  • alpha-Linolenic Acid / chemistry
  • alpha-Linolenic Acid / metabolism
  • alpha-Linolenic Acid / pharmacology*
  • gamma-Linolenic Acid / chemistry
  • gamma-Linolenic Acid / metabolism
  • gamma-Linolenic Acid / pharmacology*

Substances

  • Cardiolipins
  • Fatty Acids, Omega-3
  • alpha-Linolenic Acid
  • Oleic Acid
  • gamma-Linolenic Acid
  • Linoleic Acid
  • Fatty Acid Desaturases
  • FADS2 protein, mouse
  • CPT1B protein, mouse
  • Carnitine O-Palmitoyltransferase
  • stearidonic acid