Postprandial VLDL lipolysis products increase monocyte adhesion and lipid droplet formation via activation of ERK2 and NFκB

Laura J. den Hartigh, Robin Altman, Jennifer E. Norman, John C Rutledge

Research output: Contribution to journalArticle

20 Citations (Scopus)

Abstract

Postprandial lipemia is characterized by a transient increase in circulating triglyceride-rich lipoproteins such as very low-density lipoprotein (VLDL) and has been shown to activate monocytes in vivo. Lipolysis of VLDL releases remnant particles, phospholipids, monoglycerides, diglycerides, and fatty acids in close proximity to endothelial cells and monocytes. We hypothesized that postprandial VLDL lipolysis products could activate and recruit monocytes by increasing monocyte expression of proinflammatory cytokines and adhesion molecules, and that such activation is related to the development of lipid droplets. Freshly isolated human monocytes were treated with VLDL lipolysis products (2.28 mmol/l triglycerides + 2 U/ml lipoprotein lipase), and monocyte adhesion to a primed endothelial monolayer was observed using a parallel plate flow chamber coupled with a CCD camera. Treated monocytes showed more rolling and adhesion than controls, and an increase in transmigration between endothelial cells. The increased adhesive events were related to elevated expression of key integrin complexes including Mac-1 [αm-integrin (CD11b)/β2-integrin (CD18)], CR4 [αx-integrin (CD11c)/CD18] and VLA-4 [α4-integrin (CD49d)/β1-integrin (CD29)] on treated monocytes. Treatment of peripheral blood mononuclear cells (PBMCs) and THP-1 monocytes with VLDL lipolysis products increased expression of TNFα, IL-1β, and IL-8 over controls, with concurrent activation of NFkB and AP-1. NFκB and AP-1-induced cytokine and integrin expression was dependent on ERK and Akt phosphorylation. Additionally, fatty acids from VLDL lipolysis products induced ERK2-dependent lipid droplet formation in monocytes, suggesting a link to inflammatory signaling pathways. These results provide novel mechanisms for postprandial monocyte activation by VLDL lipolysis products, suggesting new pathways and biomarkers for chronic, intermittent vascular injury.

Original languageEnglish (US)
JournalAmerican Journal of Physiology - Heart and Circulatory Physiology
Volume306
Issue number1
DOIs
StatePublished - Jan 1 2014

Fingerprint

VLDL Lipoproteins
Lipolysis
Monocytes
Integrins
Transcription Factor AP-1
Triglycerides
Lipid Droplets
Fatty Acids
Endothelial Cells
Cytokines
Integrin alpha4beta1
Monoglycerides
Lipoprotein Lipase
Vascular System Injuries
Diglycerides
Hyperlipidemias
Interleukin-8
Interleukin-1
Adhesives
Lipoproteins

Keywords

  • Adhesion molecules
  • Fatty acids
  • Inflammation
  • Lipoprotein lipase

ASJC Scopus subject areas

  • Physiology
  • Physiology (medical)
  • Cardiology and Cardiovascular Medicine

Cite this

Postprandial VLDL lipolysis products increase monocyte adhesion and lipid droplet formation via activation of ERK2 and NFκB. / den Hartigh, Laura J.; Altman, Robin; Norman, Jennifer E.; Rutledge, John C.

In: American Journal of Physiology - Heart and Circulatory Physiology, Vol. 306, No. 1, 01.01.2014.

Research output: Contribution to journalArticle

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