Wound-healing peptides curb bacterial colonization in cystic fibrosis airway models
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Cystic fibrosis, one of the most common genetic diseases in Switzerland, promotes chronic bacterial infections by impairing the protective barrier of the airways. Scientists at the University of Geneva (UNIGE) have discovered that this dysfunction is caused by the abnormal activation of a protein, connexin 43, which disrupts cellular organization and compromises the integrity of the airways.
The team has not only shed light on this molecular mechanism using 3D models of cells derived from human lungs but has also succeeded in correcting the defect using molecules already undergoing clinical trials in dermatology and oncology. Preventing pathogenic bacteria from attaching to the airways of people with cystic fibrosis could therefore help limit serious complications.
These findings are published in the journal Communications Biology.
Despite significant therapeutic advances, chronic pulmonary infections persist in many patients with cystic fibrosis. Eradicating respiratory pathogens therefore remains a major challenge.
In previous work, Marc Chanson's team—led by Chanson, a full professor at the Department of Cell Physiology and Metabolism, the Department of Paediatrics, Gynaecology and Obstetrics, and the Geneva Centre for Inflammation Research at the UNIGE Faculty of Medicine—discovered that this vulnerability to infection stemmed from abnormal adhesion sites on the surface of respiratory cells—true "anchor points" to which bacteria attach firmly.
"But to develop treatments, we first needed to understand the underlying mechanisms," explains Chanson.
A protein behind bacterial anchor points
Connexin 43 is a protein known for its role in communication between cells, a process essential to the functioning of tissues and organs. In the airways, it is normally active only when cells need to regenerate. In people with cystic fibrosis, however, it remains abnormally active, triggering a cascade of dysfunctions.
"Using 3D models of cells derived from human lungs, we discovered that prolonged connexin 43 activity alters cell communication, disrupts cell orientation and progressively disorganizes tissue integrity," says Mehdi Badaoui, senior lecturer in the Department of Cell Physiology and Metabolism at the UNIGE Faculty of Medicine and first author of the study.
"It then promotes the formation of the anchor points to which the bacteria responsible for respiratory infections attach."
Restoring the integrity of the airways
By blocking connexin 43 activity in their 3D models, the research team was able to restore cell orientation, re-establish the spatial organization of cells and prevent the formation of anchor points.
"Mimetic peptides—short synthetic molecules already used to promote wound healing—drastically reduced the ability of bacteria to colonize respiratory cells," explains Badaoui.
"These findings demonstrate that the regulation of cell communication by connexin 43 is a fundamental element in maintaining pulmonary defense," concludes Chanson.
"By targeting the deep mechanisms underlying airway dysfunction, our results could offer an additional treatment approach."
Publication details
Mehdi Badaoui et al, Cx43 levels guide apicobasal polarity in regenerating airway epithelial cells, Communications Biology (2026). DOI: 10.1038/s42003-026-10413-7
Journal information: Communications Biology
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Pulmonary medicinePediatrics Provided by University of Geneva Who's behind this story?
Swati Mestri
Swati Mestri holds a bachelor's degree in Electronics Engineering and has worked as a content editor since 2019. She has experience editing research documents across technology, health care, and materials science, and has a particular interest in technology and space. Full profile →
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