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Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4

Porphyromonas gingivalis (P. gingivalis) is an important pathogen that contributes to periodontal disease and causes infections that promote the progression of atherosclerosis. Our previous studies showed that macrophage migration inhibitory factor (MIF) facilitates monocyte adhesion to endothelial...

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Autores principales: Wu, Yun, Xu, Wanyue, Hou, Jingya, Liu, Yanqing, Li, Rong, Liu, Jingbo, Li, Chen, Tang, Xiaolin, Lin, Li, Pan, Yaping, Zhang, Dongmei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527533/
https://www.ncbi.nlm.nih.gov/pubmed/30506423
http://dx.doi.org/10.1007/s10753-018-0942-0
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author Wu, Yun
Xu, Wanyue
Hou, Jingya
Liu, Yanqing
Li, Rong
Liu, Jingbo
Li, Chen
Tang, Xiaolin
Lin, Li
Pan, Yaping
Zhang, Dongmei
author_facet Wu, Yun
Xu, Wanyue
Hou, Jingya
Liu, Yanqing
Li, Rong
Liu, Jingbo
Li, Chen
Tang, Xiaolin
Lin, Li
Pan, Yaping
Zhang, Dongmei
author_sort Wu, Yun
collection PubMed
description Porphyromonas gingivalis (P. gingivalis) is an important pathogen that contributes to periodontal disease and causes infections that promote the progression of atherosclerosis. Our previous studies showed that macrophage migration inhibitory factor (MIF) facilitates monocyte adhesion to endothelial cells by regulating the expression of intercellular adhesion molecule-1 (ICAM-1) inP. gingivalis-infected endothelial cells. However, the detailed pathological role of MIF has yet to be elucidated in this context. To explore the functional receptor(s) of MIF that underlie its participation in the pathogenesis of atherosclerosis, we investigated the expression of the chemokine receptors CD74 and CXCR4 in endothelial cells, both of which were shown to be involved in the adhesion of monocytes to endothelial cells pretreated with P. gingivalis. Furthermore, the formation of a MIF, CD74, and CXCR4 ligand-receptor complex was revealed by our immunofluorescence staining and coimmunoprecipitation results. By interacting with the CD74/CXCR4 receptor complex, MIF may act as a crucial regulator of monocyte-endothelial cell adhesion and promote the atherosclerotic plaque formation induced by P. gingivalis.
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spelling pubmed-65275332019-06-07 Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4 Wu, Yun Xu, Wanyue Hou, Jingya Liu, Yanqing Li, Rong Liu, Jingbo Li, Chen Tang, Xiaolin Lin, Li Pan, Yaping Zhang, Dongmei Inflammation Original Article Porphyromonas gingivalis (P. gingivalis) is an important pathogen that contributes to periodontal disease and causes infections that promote the progression of atherosclerosis. Our previous studies showed that macrophage migration inhibitory factor (MIF) facilitates monocyte adhesion to endothelial cells by regulating the expression of intercellular adhesion molecule-1 (ICAM-1) inP. gingivalis-infected endothelial cells. However, the detailed pathological role of MIF has yet to be elucidated in this context. To explore the functional receptor(s) of MIF that underlie its participation in the pathogenesis of atherosclerosis, we investigated the expression of the chemokine receptors CD74 and CXCR4 in endothelial cells, both of which were shown to be involved in the adhesion of monocytes to endothelial cells pretreated with P. gingivalis. Furthermore, the formation of a MIF, CD74, and CXCR4 ligand-receptor complex was revealed by our immunofluorescence staining and coimmunoprecipitation results. By interacting with the CD74/CXCR4 receptor complex, MIF may act as a crucial regulator of monocyte-endothelial cell adhesion and promote the atherosclerotic plaque formation induced by P. gingivalis. Springer US 2018-12-03 2019 /pmc/articles/PMC6527533/ /pubmed/30506423 http://dx.doi.org/10.1007/s10753-018-0942-0 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Wu, Yun
Xu, Wanyue
Hou, Jingya
Liu, Yanqing
Li, Rong
Liu, Jingbo
Li, Chen
Tang, Xiaolin
Lin, Li
Pan, Yaping
Zhang, Dongmei
Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4
title Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4
title_full Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4
title_fullStr Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4
title_full_unstemmed Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4
title_short Porphyromonas gingivalis-Induced MIF Regulates Intercellular Adhesion Molecule-1 Expression in EA.hy926 Cells and Monocyte-Endothelial Cell Adhesion Through the Receptors CD74 and CXCR4
title_sort porphyromonas gingivalis-induced mif regulates intercellular adhesion molecule-1 expression in ea.hy926 cells and monocyte-endothelial cell adhesion through the receptors cd74 and cxcr4
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6527533/
https://www.ncbi.nlm.nih.gov/pubmed/30506423
http://dx.doi.org/10.1007/s10753-018-0942-0
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