1. Academic Validation
  2. 7-Ketocholesterol enhances leukocyte adhesion to endothelial cells via p38MAPK pathway

7-Ketocholesterol enhances leukocyte adhesion to endothelial cells via p38MAPK pathway

  • PLoS One. 2018 Jul 31;13(7):e0200499. doi: 10.1371/journal.pone.0200499.
Mariko Tani 1 Yuko Kamata 2 Michiyo Deushi 2 Mizuko Osaka 1 2 Masayuki Yoshida 2
Affiliations

Affiliations

  • 1 Department of Nutrition in Cardiovascular Disease, Tokyo Medical and Dental University, Yushima, Bunkyo-ku, Tokyo, Japan.
  • 2 Department of Life sciences and Bioethics, Tokyo Medical and Dental University, Yushima, Bunkyo-ku, Tokyo, Japan.
Abstract

7-Ketocholesterol is a major dietary Cholesterol oxidation product found in high concentrations in atherosclerotic plaques, which contribute to the development of atherosclerosis. This study aimed to investigate the effects of 7-ketocholesterol on endothelial inflammation, as well as the underlying mechanisms. Pretreatment of human umbilical vein endothelial cells (HUVEC) with 7-ketocholesterol significantly enhanced the total interactions between human monocytic cells (THP-1 cell line) and TNFα-activated HUVECs under physiological flow conditions, compared to pretreatment with Cholesterol (TNFα+50 μM cholesterol: 13.1 ± 0.54 cells/CPF, TNFα+50 μM 7-ketocholesterol: 18.9 ± 0.35 cells/CPF, p < 0.01). 7-Ketocholesterol enhanced the expression of E-Selectin, ICAM-1, and VCAM-1 proteins. It also activated p38 mitogen-activated protein kinase (MAPK), and treatment with a p38 MAPK Inhibitor inhibited both E-Selectin expression via ATF-2 activation and 7-ketocholesterol-induced THP-1 adhesion to HUVECs. These findings suggest that 7-ketocholesterol enhances leukocyte-endothelial interactions by upregulating the expression of adhesion molecules, presumably via the p38 MAPK-dependent pathway.

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