Scientists have developed a new virtual model of mouse lung function that illuminates the relative importance of different factors that contribute to lung changes accompanying chronic inflammation. Christopher Massa and his colleagues at Rutgers University, New Jersey, present the work in PLOS Computational Biology.
Chronic inflammation, which is often found in people with chronic obstructive pulmonary disease (COPD), and aging both alter lung structure and function. Respiratory impedance--a measure of air flow and pressure in the throat--can be used to model and assess general lung function. However, this approach cannot distinguish the relative impact of specific changes, such as destruction of air sacs and altered airway size.
In pursuit of a more detailed approach, Massa and colleagues examined lung tissue and function in healthy mice, as well as in mice that had been genetically engineered to mimic conditions seen in people with emphysema, a type of COPD. Then, they used this experimental data to build a new model that simulates changes in mouse lung function, as indicated by respiratory impedance.
The researchers used the model to compare the relative influence on lung function of several factors associated with chronic inflammatory disease. These included lung tissue destruction, changes in density of elastic fiber structures that aid in stretching and contraction of lung walls during breathing, and changes in lung recruitment, in which elevated pressure keeps open lung regions that might otherwise collapse.
Modeling results suggested that changes in lung recruitment and elastic fiber density were mainly responsible for the observed decrease in lung function associated with chronic inflammatory disease in the mice. This contracts with previous proposals that tissue damage and loss of structure have the greatest impact.
The new model provides a fresh approach for examining how pathological changes alter lung function. "The most exciting aspect of this research is that by conducting these analyses we can determine what has happened to the lung tissue simply by measuring air flow and pressure at the throat," says study co-author Andrew Gow.
Further work will be needed to refine the new model and determine how the results might apply to humans. Nonetheless, it opens up new pathways for research. "The next steps for this research are to directly test how well the model can predict the effects of a therapeutic intervention, such as budesonide, upon lung function," Gow says.
In your coverage please use this URL to provide access to the freely available article in PLOS Computational Biology: http://journals.plos.org/ploscompbiol/article?id=10.1371/journal.pcbi.1005570
Citation: Massa CB, Groves AM, Jaggernauth SU, Laskin DL, Gow AJ (2017) Histologic and biochemical alterations predict pulmonary mechanical dysfunction in aging mice with chronic lung inflammation. PLoS Comput Biol 13(8): e1005570. https://doi.org/10.1371/journal.pcbi.1005570
Funding: All funding is from the National Institutes of Health, https://grants.nih.gov/funding/index.htm: National Institute of Environmental Health Sciences: ES004738, ES005022, ES007148; National Institute of Arthritis and Musculoskeletal and Skin Diseases: AR055073; National Heart Lung and Blood Institute: HL086621. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing Interests: The authors have declared that no competing interests exist.
PLoS Computational Biology