Author:

Keywords:

Science & Technology, Life Sciences & Biomedicine, Respiratory System, C-reactive protein, chronic thromboembolic pulmonary hypertension, endothelial cells, inflammation, smooth muscle cells, PLASMINOGEN-ACTIVATOR INHIBITOR, AORTIC ENDOTHELIAL-CELLS, INNOCENT BYSTANDER, HIGH PREVALENCE, RISK-FACTORS, DYSFUNCTION, EXPRESSION, RELEASE, PLASMA, PLAQUE, Adult, Aged, C-Reactive Protein, Case-Control Studies, Cell Adhesion, Cell Proliferation, Cells, Cultured, Endothelial Cells, Endothelin-1, Endothelium, Vascular, Female, Humans, Hypertension, Pulmonary, Inflammation, Intercellular Adhesion Molecule-1, Male, Middle Aged, Muscle, Smooth, Vascular, Myocytes, Smooth Muscle, Pulmonary Artery, Receptors, Immunologic, Scavenger Receptors, Class E, Thromboembolism, von Willebrand Factor, 11 Medical and Health Sciences, 3201 Cardiovascular medicine and haematology

Abstract:

Chronic thromboembolic pulmonary hypertension (CTEPH) is characterised by proximal pulmonary vascular obstruction by thrombo-fibrotic material, the origin of which has not been elucidated. Enhanced inflammation could contribute to persistent obstruction by impairing pulmonary vascular cell function in CTEPH. We investigated C-reactive protein (CRP) effects on pulmonary vascular cell function in vitro. Primary cultures of proximal pulmonary endothelial cells (ECs) and smooth muscle cells (SMCs) from CTEPH and nonthromboembolic pulmonary hypertension (PH) patients were established. Recombinant CRP effects on mitogenic activity, adhesion capacity, endothelin-1 and von Willebrand factor (vWF) secretion and intercellular adhesion molecule (ICAM)-1 and vascular cell adhesion molecule-1 expression were investigated in ECs and/or SMCs. Expression of the CRP receptor, lectin-like oxidised low-density lipoprotein receptor (LOX)-1, was evaluated in proximal pulmonary arterial tissue and cells by Western blotting and immunofluorescence. CRP increased CTEPH-SMC proliferation by 250%. CRP increased adhesion capacity, endothelin-1 and vWF secretion by CTEPH-ECs by 37%, 129% and 694%, respectively. CRP-induced adhesion of CTEPH-ECs to monocytes was mediated by ICAM-1. CRP had no effect on cells from nonthromboembolic PH patients, probably because of overexpression of LOX-1 in CTEPH. Local expression of CRP was detected in ECs and SMCs within pulmonary arterial tissue. CRP may contribute to persistent obstruction of proximal pulmonary arteries in CTEPH by promoting vascular remodelling, endothelial dysfunction and in situ thrombosis.