Professor Ethan Goddard-Borger.
A discovery about how mucus thickness is regulated could help to improve airway-clearing treatment options for people with chronic respiratory conditions such as asthma, cystic fibrosis and chronic obstructive pulmonary disease (COPD).
New insights into the molecular mechanisms driving mucus viscosity were discovered by a Melbourne research team led by Associate Professor Ethan Goddard-Borger from the Walter and Eliza Hall Institute. The study was published in the journal Nature Communications.
At a glance
- Researchers have discovered the reason why the excessive amounts of mucus produced by patients with respiratory illnesses is thicker than usual.
- Mucus viscosity is driven by proteins called ‘trefoil factors’ that bind to ‘mucin glycoproteins’, long protein strands coated with unique sugar molecules.
- Understanding these mechanisms could help to significantly improve airway-clearing treatments for patients with chronic respiratory diseases.
Worldwide, hundreds of millions of people are impacted by chronic respiratory disease. COPD alone affects more than 250 million people, causing 3 million deaths each year. People with chronic respiratory diseases typically produce an excessive amount of thick mucus in the lungs which obstructs their airways, making it difficult to breathe.
Significant leap in mucus biology
Mucus is mostly comprised of water and mucin glycoproteins which are very long protein strands coated with glycans – a type of sugar molecule.
Associate Professor Goddard-Borger said the study’s findings revealed that proteins called ‘trefoil factors’ interact with mucins by recognising and binding to the unique glycan signatures on their surface.
“Trefoil factors have long been known to make mucus more viscous (thicker), and it has been postulated that this thickening occurs in respiratory diseases. However, until now we did not completely understand how the trefoil factor proteins achieved this.”
Associate Professor Goddard-Borger said the research showed trefoil factors had two glycan-binding sites and could cross-link mucins strands to make the mucus gel more rigid.
“Within mucus, trefoil factors essentially ‘staple’ the mucin strands into a mesh: the more staples, the denser the mesh and the thicker the mucus becomes.”
Understanding what trefoil factors bind to and how they do this represents a significant leap forward in understanding mucus and how it functions in the respiratory, gastrointestinal and reproductive tracts.
Improving therapies for blocked airways
Associate Professor Goddard-Borger said that going forward the aim was to inhibit the bonds created between trefoil factors and mucin strands, and that the development of such a technology could lead to new therapeutics for the treatment of respiratory diseases.
“A healthy amount of mucus is very important for capturing and clearing potential threats to the lung, such as dust particles, dead cells and bacteria, so we’re not looking to remove mucus altogether.
“We are seeking to develop innovative approaches for reducing the viscosity of the mucus to aid in clearing excess mucus from the lungs of patients with chronic respiratory disease.”
“The next step is to work with commercial collaborators to progress our vision to develop new mucolytic drugs that can more effectively clear mucus from the airways. Achieving this could make a significant impact on the quality of life and life expectancy of people struggling with debilitating respiratory conditions,” Associate Professor Goddard-Borger said.
The study was supported by the National Health and Medical Research Council of Australia (NHMRC) and the Victorian Government.