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Updated: Apr 27, 2026

Alveolar Macrophage Phagocytosis and Bacteria Clearance in Mice
Published on: March 2, 2019
Impact of alginate-producing Pseudomonas aeruginosa on alveolar macrophage apoptotic cell clearance
Charlie A McCaslin1, Daniela N Petrusca2, Christophe Poirier2
1Department of Pediatrics, Pediatric Pulmonology, Indiana University Purdue University Indianapolis, Indianapolis, IN.
Abstract:
Pseudomonas aeruginosa infection is a hallmark of lung disease in cystic fibrosis. Acute infection with P. aeruginosa profoundly inhibits alveolar macrophage clearance of apoptotic cells (efferocytosis) via direct effect of virulence factors. During chronic infection, P. aeruginosa evades host defense by decreased virulence, which includes the production or, in the case of mucoidy, overproduction of alginate. The impact of alginate on innate immunity, in particular on macrophage clearance of apoptotic cells is not known. We hypothesized that P. aeruginosa strains that exhibit reduced virulence impair macrophage clearance of apoptotic cells and we investigated if the polysaccharide alginate produced by mucoid P. aeruginosa is sufficient to inhibit alveolar macrophage efferocytosis. Rat alveolar or human peripheral blood monocyte (THP-1)-derived macrophage cell lines were exposed in vitro to exogenous alginate or to wild type or alginate-overproducing mucoid P. aeruginosa prior to challenge with apoptotic human Jurkat T-lymphocytes. The importance of LPS contamination and that of structural integrity of alginate polymers was tested using alginate of different purities and alginate lyase, respectively. Alginate inhibited alveolar macrophage efferocytosis in a dose- and time-dependent manner. This effect was augmented but not exclusively attributed to lipopolysaccharide (LPS) present in alginates. Alginate-producing P. aeruginosa inhibited macrophage efferocytosis by more than 50%. A mannuronic-specific alginate lyase did not restore efferocytosis inhibited by exogenous guluronic-rich marine alginate, but had a marked beneficial effect on efferocytosis of alveolar macrophages exposed to mucoid P. aeruginosa. Despite decreased virulence, mucoid P. aeruginosa may contribute to chronic airway inflammation through significant inhibition of alveolar clearance of apoptotic cells and debris. The mechanism by which mucoid bacteria inhibit efferocytosis may involve alginate production and synergy with LPS, suggesting that alginate lyase may be an attractive therapeutic approach to airway inflammation in cystic fibrosis and other chronic obstructive pulmonary diseases characterized by P. aeruginosa colonization.
Insights
Pseudomonas aeruginosa alginate inhibits macrophage clearance of apoptotic cells, contributing to cystic fibrosis lung inflammation. Alginate lyase may offer a therapeutic approach.
Area of Science:
- Immunology
- Microbiology
- Pulmonary Medicine
Background:
- Pseudomonas aeruginosa infection is central to cystic fibrosis lung disease.
- During chronic infection, P. aeruginosa reduces virulence, often overproducing alginate.
- The effect of alginate on macrophage efferocytosis (clearance of apoptotic cells) is unknown.
Purpose of the Study:
- To investigate if alginate produced by mucoid P. aeruginosa inhibits macrophage efferocytosis.
- To determine if alginate alone is sufficient to impair efferocytosis.
- To explore alginate lyase as a potential therapeutic.
Main Methods:
- In vitro exposure of rat alveolar or human THP-1 derived macrophages to alginate or mucoid P. aeruginosa.
- Challenge with apoptotic human Jurkat T-lymphocytes.
- Testing alginate purity and alginate lyase activity.
Main Results:
- Alginate dose- and time-dependently inhibited macrophage efferocytosis.
- Lipopolysaccharide (LPS) contamination augmented this inhibition.
- Mucoid P. aeruginosa significantly inhibited efferocytosis; alginate lyase partially restored it.
Conclusions:
- Alginate contributes to P. aeruginosa's immune evasion by inhibiting efferocytosis.
- Alginate's synergy with LPS may drive chronic airway inflammation in cystic fibrosis.
- Alginate lyase presents a potential therapeutic strategy for P. aeruginosa-related lung diseases.

