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Updated: Apr 30, 2026

Utilizing the Precision-Cut Lung Slice to Study the Contractile Regulation of Airway and Intrapulmonary Arterial Smooth Muscle
Published on: May 5, 2022
The contractile response of isolated small pulmonary arteries induced by activated macrophages
M Zaloudíková1, J Herget, M Vízek
1Department of Pathophysiology, Second Faculty of Medicine, Charles University, Prague, Czech Republic. marie.zaloudikova@lfmotol.cuni.cz.
Abstract:
To test whether macrophages can play any role in hypoxic pulmonary vasoconstriction, we tested the in vitro response of rings from small pulmonary arteries to the activation of macrophages by FMLP, a substance stimulating predominantly membrane-bound NADPH oxidase. A small vessel myograph was used to measure the responses of rings from small pulmonary arteries (300-400 microm) isolated from rat lungs. Rings from 5 rats were placed into both chambers of the myograph. The vessels were stabilized for 40 min and then normalized by automatic stretching to a wall tension equivalent to the intravascular pressure 30 mm Hg. At the start of each experiment, vessels were exposed to 80 mM K+ to obtain maximal contractile response, which was used to normalize subsequent contractile responses. 2x10(6) viable macrophages, obtained by peritoneal lavage, were added into one chamber, then 5 microM FMLP was administrated to both chambers and the tension measurement was started. The hydrogen peroxide concentration produced by stimulated macrophages was measured luminometrically. The concentrations of H2O2 in specimens from chambers containing activated macrophages rose from 3.5+/-1.5 nM to 110+/-28 nM within 25 min of stimulation, while FMLP itself didn't increase the H2O2 concentration from the baseline value (4.5+/-3 nM) in samples from control chambers. After FMLP administration, the tension of the vessel rings in the presence of macrophages reached 0.23+/-0.07 of maximal contractile response, it did not change in controls. The addition of ROS scavenger 4-hydroxy-TEMPO blocked the contractile response to the activation of macrophages. We conclude that the activation of macrophages stimulates the contraction of small pulmonary arteries and that this contraction is probably mediated by reactive oxygen species.
Insights
Activated macrophages stimulate pulmonary artery contraction via reactive oxygen species (ROS). This finding suggests a new pathway in hypoxic pulmonary vasoconstriction, involving macrophage-derived ROS.
Area of Science:
- Pulmonary Physiology
- Immunology
- Vascular Biology
Background:
- Hypoxic pulmonary vasoconstriction (HPV) is a critical physiological response.
- The role of immune cells, specifically macrophages, in HPV remains incompletely understood.
Purpose of the Study:
- To investigate the potential role of macrophages in mediating pulmonary artery contraction.
- To determine if macrophage activation can influence the contractile state of small pulmonary arteries.
Main Methods:
- Isolated rat small pulmonary artery rings (300-400 µm) were studied using a small vessel myograph.
- Macrophages were activated using N-formyl-methionyl-leucyl-phenylalanine (FMLP), stimulating NADPH oxidase.
- Hydrogen peroxide (H2O2) production and vessel tension were measured; reactive oxygen species (ROS) scavenger was used to confirm mediation.
Main Results:
- FMLP-activated macrophages significantly increased H2O2 production.
- Pulmonary artery rings in the presence of activated macrophages exhibited significant contraction (0.23±0.07 of maximal response).
- The contraction was abolished by a ROS scavenger, implicating ROS in the response.
Conclusions:
- Macrophage activation induces contraction in small pulmonary arteries.
- This contraction is likely mediated by reactive oxygen species produced by activated macrophages.
- Macrophages may play a significant role in the mechanisms of hypoxic pulmonary vasoconstriction.

