Human Lung Macrophages Challenged to Oxidants ex vivo: Lysosomal Membrane Sensitization is Associated with Inflammation and Chronic Airflow Limitation

• Published in: Journal of inflammation research Vol. 13; pp. 925 - 932
• Main Authors: Persson, Hans Lennart, Sioutas, Apostolos, Jacobson, Petra, Vainikka, Linda K
• Format: Journal Article
• Language: English
• Published: New Zealand Dove Medical Press Limited 01.01.2020; Taylor & Francis Ltd; Dove; Dove Medical Press
• Subjects: Acridine orange; Alveoli; Asthma; Autophagy; bal; Bronchoscopy; Cellular stress response; Chronic obstructive pulmonary disease; copd; Experiments; Fibroblasts; Fibrosis; Fluorescence; Inflammation; Inflammatory diseases; lmp; Lung diseases; Lung diseases, Obstructive; lung macrophages; Lungs; Lysosomes; Macrophages; Original Research; Oxidants; Oxidative stress; pulmonary fibrosis; Respiratory tract; Respiratory tract diseases; Sarcoidosis; Smoking; Spirometry; Tobacco; Wound healing; Sweden; United Kingdom > UK; BAL; LMP; acridine orange; lung macrophages; pulmonary fibrosis; COPD
• ISSN: 1178-7031; 1178-7031
• DOI: 10.2147/JIR.S280419

The lung macrophage (LM) is involved in most inflammatory processes of the human lung by clearance of dying cells and by wound repair. Upon cellular stress by oxidant challenge in vivo lysosomes may rupture in LMs and leakage of cellular content and cell debris may trigger airway inflammation and fibrosis, which may lead to chronic airflow limitation (CAL). The aim of this study was to determine whether lysosomal membrane permeabilization (LMP) in LMs challenged to oxidants ex vivo is associated with airway inflammation and CAL, the latter assessed as the reduced forced expiratory volume in one second (FEV ) expressed as % of predicted. Twenty-eight subjects were investigated; 13 lung-healthy subjects and 15 subjects with a variety of inflammatory disorders, demonstrating CAL on dynamic spirometry (defined as an FEV /FVC ratio < 0.70). LMs were harvested by broncho-alveolar lavage (BAL) and challenged ex vivo by oxidants. LMP in oxidant-exposed LMs was assessed as the emitted acridine orange (AO) green fluorescence from oxidant-exposed LMs (using macrophage-like murine J774 cells as positive controls). Inflammatory cells in BAL were counted and lung volumes were recorded. Oxidant-induced LMP in LMs was significantly greater among subjects with CAL and particularly among those with ongoing inflammation. Previous tobacco history did not influence LMP. Among subjects with CAL, oxidant-induced LMP correlated negatively with FEV % of predicted. Lysosomes of LMs harvested from patients with CAL demonstrate an increased sensitivity to oxidants, which may trigger mechanisms behind CAL, eg, chronic airway inflammation and fibrotic re-modelling. The study suggests a mechanistic role for LMP in LMs on airway inflammation, suggesting an anti-inflammatory effect by drugs that prevent increased LMP.