Defective bacterial phagocytosis is associated with dysfunctional mitochondria in COPD macrophages

• Published in: The European respiratory journal Vol. 54; no. 4; p. 1802244
• Main Authors: Belchamber, Kylie B.R., Singh, Richa, Batista, Craig M., Whyte, Moira K., Dockrell, David H., Kilty, Iain, Robinson, Matthew J., Wedzicha, Jadwiga A., Barnes, Peter J., Donnelly, Louise E.
• Format: Journal Article
• Language: English
• Published: England 01.10.2019
• Subjects: Aged; Bacteria; Cell Survival; Female; Haemophilus influenzae; Humans; In Vitro Techniques; Macrophages - immunology; Macrophages - metabolism; Macrophages - pathology; Macrophages, Alveolar - immunology; Macrophages, Alveolar - metabolism; Macrophages, Alveolar - pathology; Male; Membrane Potential, Mitochondrial; Microscopy, Confocal; Middle Aged; Mitochondria - metabolism; Phagocytosis - immunology; Pulmonary Disease, Chronic Obstructive - immunology; Pulmonary Disease, Chronic Obstructive - metabolism; Reactive Oxygen Species - metabolism; Streptococcus pneumoniae
• ISSN: 0903-1936; 1399-3003; 1399-3003
• DOI: 10.1183/13993003.02244-2018

Increased reactive oxygen species (ROS) have been implicated in the pathophysiology of chronic obstructive pulmonary disease (COPD). This study examined the effect of exogenous and endogenous oxidative stress on macrophage phagocytosis in patients with COPD. Monocyte-derived macrophages (MDMs) were generated from non-smoker, smoker and COPD subjects, differentiated in either granulocyte macrophage-colony stimulating factor (G-Mφ) or macrophage-colony stimulating factor (M-Mφ). Alveolar macrophages were isolated from lung tissue or bronchoalveolar lavage fluid. Macrophages were incubated in ±200 µM H 2 O 2 for 24 h, then exposed to fluorescently labelled Haemophilus influenzae or Streptococcus pneumoniae for 4 h, after which phagocytosis, mitochondrial ROS (mROS) and mitochondrial membrane potential (ΔΨm) were measured. Phagocytosis of bacteria was significantly decreased in both G-Mφ and M-Mφ from COPD patients compared with from non-smoker controls. In non-smokers and smokers, bacterial phagocytosis did not alter mROS or ΔΨm; however, in COPD, phagocytosis increased early mROS and decreased ΔΨm in both G-Mφ and M-Mφ. Exogenous oxidative stress reduced phagocytosis in non-smoker and COPD alveolar macrophages and non-smoker MDMs, associated with reduced mROS production. COPD macrophages show defective phagocytosis, which is associated with altered mitochondrial function and an inability to regulate mROS production. Targeting mitochondrial dysfunction may restore the phagocytic defect in COPD.