Triglyceride-rich lipoproteins prime aortic endothelium for an enhanced inflammatory response to tumor necrosis factor-α

Harold J. Ting, James P. Stice, Ulrich Y. Schaff, David Y. Hui, John C Rutledge, Anne A Knowlton, Anthony G. Passerini, Scott I. Simon

Research output: Contribution to journalArticlepeer-review

117 Scopus citations


High levels of triglyceride-rich lipoproteins (TGRLs) in blood are linked to development of atherosclerosis, yet the mechanisms by which these particles initiate inflammation of endothelium are unknown. TGRL isolated from human plasma during the postprandial state was examined for its capacity to bind to cultured human aortic endothelial cells (HAECs) and alter the acute inflammatory response to tumor necrosis factor-α. HAECs were repetitively incubated with dietary levels of freshly isolated TGRL for 2 hours per day for 1 to 3 days to mimic postprandial lipidemia. TGRL induced membrane upregulation of the low-density lipoprotein family receptors LRP and LR11, which was inhibited by the low-density lipoprotein receptor-associated protein-1. TGRLs alone did not elicit inflammation in HAECs but enhanced the inflammatory response via a 10-fold increase in sensitivity to cytokine stimulation. This was reflected by increased mitogen-activated protein kinase activation, nuclear translocation of NF-κB, amplified expression of endothelial selectin and VCAM-1, and a subsequent increase in monocyte-specific recruitment under shear flow as quantified in a microfabricated vascular mimetic device.

Original languageEnglish (US)
Pages (from-to)381-390
Number of pages10
JournalCirculation Research
Issue number3
StatePublished - Feb 2007


  • Atherosclerosis
  • Endothelium
  • Monocyte
  • NFκB
  • Triglyceride-rich lipoprotein
  • Vascular adhesion molecule-1

ASJC Scopus subject areas

  • Physiology
  • Cardiology and Cardiovascular Medicine


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