The role of lipolysis in mediating the proinflammatory effects of very low density lipoproteins in mouse peritoneal macrophages

Viswanathan Saraswathi, Alyssa H. Hasty

Research output: Contribution to journalArticle

62 Citations (Scopus)

Abstract

Hypertriglyceridemia is an important risk factor for atherosclerosis, especially in obesity. Macrophages are one of the primary cell types involved in atherogenesis and are thought to contribute to lesion formation through both lipid accumulation and proinflammatory gene expression. In this study, we sought to determine the direct impact of triglyceride (TG)-rich VLDL-induced lipid accumulation on macrophage proinflammatory processes. Incubation of mouse peritoneal macrophages with 100 mg/ml VLDL for 6 h led to 2.8- and 3.7-fold increases in intracellular TGs and FFAs, respectively (P < 0.05). The inflammatory proteins tumor necrosis factor-α, interleukin-1β, monocyte chemoattractant protein-1, intercellular adhesion molecule-1, matrix metalloproteinase 3 (MMP3), and macrophage inflammatory protein-1α (MIP-1α) were all upregulated by at least 2-fold (P < 0.05) in a dose-dependent manner in VLDL-treated macrophages. The increase in inflammatory gene expression coincided with the phosphorylation of the mitogen-activated protein kinase (MAPK) pathway members extracellular signal-regulated kinase (ERK) 1/2, stress-activated protein kinase/c-Jun NH2-terminal kinase, and p38 MAPK and was ameliorated by U0126, an inhibitor of ERK1/2. Inhibition of extracellular TG hydrolysis with tetrahydrolipstatin (Orlistat) resulted in the absence of intracellular TG and FFA accumulation and was accompanied by the amelioration of ERK1/2 phosphorylation and MIP-1α gene expression. These data indicate that VLDL hydrolysis, and the subsequent accumulation of intracellular FFAs and TGs, plays a substantive role in mediating the proinflammatory effects of VLDL. These data have important implications for the direct proatherogenic effects of VLDL onmacrophage-driven atherosclerosis.

Original languageEnglish (US)
Pages (from-to)1406-1415
Number of pages10
JournalJournal of Lipid Research
Volume47
Issue number7
DOIs
StatePublished - Jul 24 2006

Fingerprint

VLDL Lipoproteins
Macrophages
Lipolysis
Peritoneal Macrophages
Macrophage Inflammatory Proteins
Atherosclerosis
Gene expression
Gene Expression
Phosphorylation
Triglycerides
Hydrolysis
Lipids
Mitogen-Activated Protein Kinase 11
Matrix Metalloproteinase 3
Mitogen-Activated Protein Kinase 3
JNK Mitogen-Activated Protein Kinases
Chemokine CCL2
Hypertriglyceridemia
Mitogen-Activated Protein Kinase 1
p38 Mitogen-Activated Protein Kinases

Keywords

  • Gene expression
  • Inflammation
  • Mitogen-activated protein kinases

ASJC Scopus subject areas

  • Biochemistry
  • Endocrinology
  • Cell Biology

Cite this

The role of lipolysis in mediating the proinflammatory effects of very low density lipoproteins in mouse peritoneal macrophages. / Saraswathi, Viswanathan; Hasty, Alyssa H.

In: Journal of Lipid Research, Vol. 47, No. 7, 24.07.2006, p. 1406-1415.

Research output: Contribution to journalArticle

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