Structures & functions in the gas exchange system table

Describe the cause of cystic fibrosis and explain how cystic fibrosis affects the function of the lungs
Cystic fibrosis is caused by a recessive allele of the CFTR gene. Cystic fibrosis affects the lungs by goblet cells producing thick, sticky and dehydrated mucus. This mucus is much harder for cilia to sweep up the trachea and to the mouth and so mucus accumulates in the airways. As the mucus traps bacteria but the mucus can’t be removed, this leads to frequent infections and eventually scar tissue in the lungs. The fact that mucus obstructs the airways means that gas exchange is less efficient as it is harder for oxygen to reach the lungs and harder for carbon dioxide to be exhaled, causing breathing problems.
Make sure that you don’t confuse the cilia in the respiratory system for microvilli in the small intestine. At first glance they appear similar, but they have very different functions! Cilia are for sweeping mucus while microvilli are for the absorption of nutrients.
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