Primed polymorphonuclear leukocytes from hemodialysis patients enhance monocyte transendothelial migration
- PMID: 28778910
- DOI: 10.1152/ajpheart.00122.2017
Primed polymorphonuclear leukocytes from hemodialysis patients enhance monocyte transendothelial migration
Abstract
Increased counts and priming of peripheral polymorphonuclear leukocytes (PMNLs) are associated with future or ongoing atherosclerosis; however, the role of PMNLs in enhancing monocyte transendothelial migration is still unclear. Our aims were to examine endothelial and monocyte activation, transmigration, and posttransmigration activation induced ex vivo by in vivo primed PMNLs and the effect of antioxidants on the activation. A unique ex vivo coculture system of three cell types was developed in this study, enabling interactions among the following: primary human umbilical vein endothelial cells (HUVECs), monocytes (THP-1 cell line), and in vivo primed PMNLs from hemodialysis (HD) patients and healthy control (HC) subjects. The interactions among these cells were examined, and an intervention with superoxide dismutase and catalase was performed. Preexposed HUVECs to HD/HC PMNLs showed a significant monocyte transmigration yield, 120-170% above HCs. Monocyte exposure to HD PMNLs induced pre- and posttransmigration activation. When the three cell types were cocultivated at the same time, monocyte chemoattractant protein-1 protein levels released from HUVECs, and activation markers on HUVECs [CD54 and chemokine (C-X3-C motif) ligand 1] and monocytes [chemokine (C-X3-C) receptor 1 and chemokine (C-C motif) receptor 2] were increased. Monocyte transmigration yield decreased to 70% (compared with HC subjects) due to adherence and accumulation of monocytes to HUVECs. When superoxide dismutase and catalase were used, reduced HUVEC and monocyte activation markers brought the transmigration yields to control levels and abolished accumulation of monocytes, emphasizing the role of superoxide in this process. We conclude that peripheral primed PMNLs play a pivotal role in enhancing monocyte transendotelial migration, the hallmark of the atherosclerotic process. Primed PMNLs can be used as a mediator and a biomarker of atherosclerosis even before plaque formation.NEW & NOTEWORTHY Primed polymorphonuclear leukocytes are key mediators in monocyte transendothelial migration, a new understanding of the initiation of endothelial dysfunction and monocyte activation, transmigration, and accumulation in the subendothelial layer.
Keywords: PMNL priming; atherosclerosis risk factors; endothelial dysfunction; monocyte transmigration.
Copyright © 2017 the American Physiological Society.
Similar articles
-
Are primed polymorphonuclear leukocytes contributors to the high heparanase levels in hemodialysis patients?Am J Physiol Heart Circ Physiol. 2008 Feb;294(2):H651-8. doi: 10.1152/ajpheart.00952.2007. Epub 2007 Nov 21. Am J Physiol Heart Circ Physiol. 2008. PMID: 18032524
-
Blockade of monocyte-endothelial trafficking by transduced Tat-superoxide dismutase protein.Int J Mol Med. 2016 Feb;37(2):387-97. doi: 10.3892/ijmm.2015.2444. Epub 2015 Dec 23. Int J Mol Med. 2016. PMID: 26707483 Free PMC article.
-
CD11/CD18-independent transendothelial migration of human polymorphonuclear leukocytes and monocytes: involvement of distinct and unique mechanisms.J Leukoc Biol. 1995 Apr;57(4):553-61. doi: 10.1002/jlb.57.4.553. J Leukoc Biol. 1995. PMID: 7722414
-
Adhesion molecules mediating neutrophil migration to arthritis in vivo and across endothelium and connective tissue barriers in vitro.Inflamm Res. 1998 Oct;47 Suppl 3:S123-32. doi: 10.1007/s000110050300. Inflamm Res. 1998. PMID: 9831314 Review.
-
Dysregulated iron metabolism in patients on hemodialysis.Contrib Nephrol. 2015;185:22-31. doi: 10.1159/000380967. Epub 2015 May 19. Contrib Nephrol. 2015. PMID: 26023012 Review.
Cited by
-
The Regulation of Neutrophil Migration in Patients with Sepsis: The Complexity of the Molecular Mechanisms and Their Modulation in Sepsis and the Heterogeneity of Sepsis Patients.Cells. 2023 Mar 24;12(7):1003. doi: 10.3390/cells12071003. Cells. 2023. PMID: 37048076 Free PMC article. Review.
-
Monocytes in Uremia.Toxins (Basel). 2020 May 21;12(5):340. doi: 10.3390/toxins12050340. Toxins (Basel). 2020. PMID: 32455723 Free PMC article. Review.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials
Miscellaneous