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Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration
The leukocyte recruitment and transmigration across the endothelial barrier into the vessel wall are crucial steps in atherosclerosis. Leukocyte trafficking on the endothelium is elicited by induction of endothelial adhesion molecules, and its transmigration is mediated by degradation of basement me...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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The Korean Nutrition Society and the Korean Society of Community Nutrition
2007
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2849036/ https://www.ncbi.nlm.nih.gov/pubmed/20368952 http://dx.doi.org/10.4162/nrp.2007.1.4.285 |
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author | Kim, Dong Shoo Kwon, Hyang-Mi Choi, Jung-Suk Kang, Sang-Wook Ji, Geun-Eog Kang, Young-Hee |
author_facet | Kim, Dong Shoo Kwon, Hyang-Mi Choi, Jung-Suk Kang, Sang-Wook Ji, Geun-Eog Kang, Young-Hee |
author_sort | Kim, Dong Shoo |
collection | PubMed |
description | The leukocyte recruitment and transmigration across the endothelial barrier into the vessel wall are crucial steps in atherosclerosis. Leukocyte trafficking on the endothelium is elicited by induction of endothelial adhesion molecules, and its transmigration is mediated by degradation of basement membrane proteins through enzymatic activity of matrix metalloproteinases (MMP). The current study investigated whether resveratrol, a polyphenol present in grapes and red wine, was capable of inhibiting leukocyte adhesion to tumor necrosis factor (TNF)-α-activated endothelium. It was found that resveratrol inhibited the TNF-α-activated endothelial expression of vascular cell adhesion molecule-1 in a dose-dependent manner. In addition, resveratrol hampered THP-1 monocyte adhesion to activated endothelial cells. This study further examined whether resveratrol interfered with transendothelial migration of leukocytes. The MMP-2 gelatinolytic activity of endothelial cells was enhanced by TNF-α, which was attenuated by an addition of ≥25 µM resveratrol. In addition, 25 µM resveratrol mitigated the MMP-9 activity of THP-1 cells, followed by a marked inhibition of transendothelial migration. These results demonstrated that resveratrol suppressed monocyte adhesion and migration induced by TNF-α through modulating expression of adhesion molecules and gelatinolytic activity of MMP. These findings suggest that dietary resveratrol may be therapeutic agent for inhibiting leukocyte recruitment into the subendothelium during inflammatory atherosclerosis. |
format | Text |
id | pubmed-2849036 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | The Korean Nutrition Society and the Korean Society of Community Nutrition |
record_format | MEDLINE/PubMed |
spelling | pubmed-28490362010-04-05 Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration Kim, Dong Shoo Kwon, Hyang-Mi Choi, Jung-Suk Kang, Sang-Wook Ji, Geun-Eog Kang, Young-Hee Nutr Res Pract Original Research The leukocyte recruitment and transmigration across the endothelial barrier into the vessel wall are crucial steps in atherosclerosis. Leukocyte trafficking on the endothelium is elicited by induction of endothelial adhesion molecules, and its transmigration is mediated by degradation of basement membrane proteins through enzymatic activity of matrix metalloproteinases (MMP). The current study investigated whether resveratrol, a polyphenol present in grapes and red wine, was capable of inhibiting leukocyte adhesion to tumor necrosis factor (TNF)-α-activated endothelium. It was found that resveratrol inhibited the TNF-α-activated endothelial expression of vascular cell adhesion molecule-1 in a dose-dependent manner. In addition, resveratrol hampered THP-1 monocyte adhesion to activated endothelial cells. This study further examined whether resveratrol interfered with transendothelial migration of leukocytes. The MMP-2 gelatinolytic activity of endothelial cells was enhanced by TNF-α, which was attenuated by an addition of ≥25 µM resveratrol. In addition, 25 µM resveratrol mitigated the MMP-9 activity of THP-1 cells, followed by a marked inhibition of transendothelial migration. These results demonstrated that resveratrol suppressed monocyte adhesion and migration induced by TNF-α through modulating expression of adhesion molecules and gelatinolytic activity of MMP. These findings suggest that dietary resveratrol may be therapeutic agent for inhibiting leukocyte recruitment into the subendothelium during inflammatory atherosclerosis. The Korean Nutrition Society and the Korean Society of Community Nutrition 2007 2007-12-31 /pmc/articles/PMC2849036/ /pubmed/20368952 http://dx.doi.org/10.4162/nrp.2007.1.4.285 Text en ©2007 The Korean Nutrition Society and the Korean Society of Community Nutrition http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Research Kim, Dong Shoo Kwon, Hyang-Mi Choi, Jung-Suk Kang, Sang-Wook Ji, Geun-Eog Kang, Young-Hee Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration |
title | Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration |
title_full | Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration |
title_fullStr | Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration |
title_full_unstemmed | Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration |
title_short | Resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration |
title_sort | resveratrol blunts tumor necrosis factor-α-induced monocyte adhesion and transmigration |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2849036/ https://www.ncbi.nlm.nih.gov/pubmed/20368952 http://dx.doi.org/10.4162/nrp.2007.1.4.285 |
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