Hepatic stellate cell activation: A source for bioactive lipids

Biochim Biophys Acta Mol Cell Biol Lipids. 2019 May;1864(5):629-642. doi: 10.1016/j.bbalip.2019.02.004. Epub 2019 Feb 5.

Abstract

Hepatic stellate cells (HSCs) are non-parenchymal liver cells that characteristically contain multiple retinoid (vitamin A)-containing lipid droplets. In this study, we addressed the metabolic fate of non-retinoid lipids originating from lipid droplet loss during HSCs activation. UPLC/MS/MS and qRT-PCR were used to monitor the lipid composition and mRNA expression of selected genes regulating lipid metabolism in freshly isolated, overnight-, 3- and 7-day cultures or primary mouse HSCs. A preferential accumulation of specific C20-C24 fatty acid species, especially arachidonic (C20:4) and docosahexaenoic acids (C22:6), was revealed in culture-activated HSCs along with an upregulation of transcription of fatty acid desaturases (Scd1, Scd2) and elongases (Elovl5, Elovl6). This was accompanied with an enrichment of activated HSCs with 36:4 and 38:4 phosphatidylcholine species containing polyunsaturated fatty acids and associated accumulation of selective lipid mediators, including endocannabinoids and related N-acylethanolamides, as well as ceramides. An increase in 2-arachidonoylglycerol and N-arachydonoylethanolamide concentrations was observed along with an upregulation of Daglα mRNA expression in HSCs during culture activation. N-palmitoylethanolamide was identified as the most abundant endocannabinoid-like species in activated HSCs. An increase in total ceramide levels and enrichment with N-palmitoyl (C16:0), N-tetracosenoyl (C24:1), N-tetracosanoyl (C24:0) and N-docosanoyl (C22:0) ceramides was detected in activated HSC cultures and was preceded by increased mRNA expression of ceramide synthesizing enzymes (CerS2, CerS5 and Smpd1). Our data suggest an active redistribution of non-retinoid lipids in HSCs underlying the formation of low abundance, highly bioactive lipid species that may affect signaling during HSC activation, as well as extracellularly within the liver.

Keywords: Ceramides; Endocannabinoids; Lipid droplets; Lipidomics; Phosphatidylcholine; Polyunsaturated fatty acids.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cells, Cultured
  • Ceramides / metabolism
  • Endocannabinoids / metabolism
  • Fatty Acids, Unsaturated / metabolism
  • Hepatic Stellate Cells / metabolism*
  • Lipid Droplets / metabolism*
  • Male
  • Metabolome
  • Mice, Inbred C57BL
  • Phosphatidylcholines / metabolism

Substances

  • Ceramides
  • Endocannabinoids
  • Fatty Acids, Unsaturated
  • Phosphatidylcholines