Prof Michael Crooks m.g.crooks@hull.ac.uk
Professor of Respiratory Medicine
Increased platelet binding to circulating monocytes in idiopathic pulmonary fibrosis.
Crooks, Michael; Fahim, Ahmed; Hart, Simon; Crooks, Michael G.; Morice, Alyn; Morice, Alyn H.; Hart, Simon P.
Authors
Ahmed Fahim
Professor Simon Hart S.Hart@hull.ac.uk
Professor in Respiratory Medicine
Prof Michael Crooks m.g.crooks@hull.ac.uk
Professor of Respiratory Medicine
Professor Alyn Morice A.H.Morice@hull.ac.uk
Foundation Chair and Professor of Respiratory Medicine
Professor Alyn Morice A.H.Morice@hull.ac.uk
Foundation Chair and Professor of Respiratory Medicine
Professor Simon Hart S.Hart@hull.ac.uk
Professor in Respiratory Medicine
Abstract
Purpose Idiopathic pulmonary fibrosis (IPF) is the most common idiopathic interstitial pneumonia and its prognosis is poor. Epidemiological evidence suggests an association of IPF with vascular disease and thrombotic tendency, which may be related to platelet activation. Methods Platelet–monocyte adhesion in peripheral blood was examined by flow cytometry in patients with IPF (n = 19), interstitial lung disease (ILD) other than IPF (n = 9), and control subjects without pulmonary fibrosis (n = 14). Expression of platelet activation markers P-selectin (CD62P), PSGL-1 (CD162), and CD40 ligand (CD40L) on leukocytes and platelets were studied. Plasma concentrations of soluble P-selectin and CD40L were measured by ELISA. Results Significantly elevated levels of platelet–monocyte binding were found in patients with IPF (35.6 ± 4.34 % [mean ± SEM]) compared with patients with non-IPF ILD (23.5 ± 3.68 %) and non-ILD control subjects (16.5 ± 2.26 %; P < 0.01). There was a trend towards increased divalent cation-independent platelet–monocyte binding in IPF (6.0 ± 0.77 % [mean ± SEM]) compared with non-IPF ILD (4.3 ± 1.38 %) and control subjects without ILD (3.1 ± 1.75 %; P = 0.058). There was no differential surface expression of platelet activation markers on subsets of leukocytes or platelets. Plasma concentrations of CD40L and soluble P-selectin did not differ between IPF and control subjects. Platelet–monocyte binding had no significant correlation with percent predicted TLco or FVC. Conclusions Platelet–monocyte binding is increased in IPF, suggesting increased platelet activation. This conjugation is predominantly calcium-dependent, but there may be more calcium-independent adhesion in IPF. These findings support further research into the role of platelet activation in IPF.
Citation
Fahim, A., Crooks, M. G., Morice, A. H., & Hart, S. P. (2014). Increased platelet binding to circulating monocytes in idiopathic pulmonary fibrosis. Lung, 192(2), 277-284. https://doi.org/10.1007/s00408-013-9546-5
Journal Article Type | Article |
---|---|
Acceptance Date | Dec 14, 2013 |
Online Publication Date | Jan 7, 2014 |
Publication Date | 2014-04 |
Deposit Date | Mar 16, 2017 |
Journal | Lung |
Print ISSN | 0341-2040 |
Publisher | Springer Verlag |
Peer Reviewed | Peer Reviewed |
Volume | 192 |
Issue | 2 |
Pages | 277-284 |
DOI | https://doi.org/10.1007/s00408-013-9546-5 |
Keywords | Idiopathic pulmonary fibrosis, Interstitial lung disease, Monocytes, Platelets, Platelet-monocyte complexes |
Public URL | https://hull-repository.worktribe.com/output/449719 |
Publisher URL | https://link.springer.com/article/10.1007/s00408-013-9546-5 |
Additional Information | This is a description of an article published in Lung, 2014, v.192 issue 2. It is not available in this repository. |
Contract Date | Mar 16, 2017 |
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