The diagram below shows a typical epithelial cell from the lining of the airways. The stickiness of mucus in the airways is controlled by CFTR chloride ion channels.
When there is too little water in the mucus the CFTR channel opens, allowing Cl- ions to move into the mucus. When active, the CFTR channel also inhibits the activity of sodium channels and limits movement of Na+ ions into the cells. The resulting high concentration of salt in the mucus draws water out of the cells, making the mucus less sticky.
Cystic fibrosis is a genetic disorder characterised by a build-up of thick, sticky mucus that damages the function of the airways and digestive system. People with class I cystic fibrosis have inherited two faulty versions of the gene that codes for CFTR, resulting in non-functioning CFTR channels.
(i)
Suggest how a lack of functioning CFTR channel impacts the movement of Na+ and Cl- ions across epithelial cells.
[3]
(ii)
Explain why the mucus of cystic fibrosis sufferers is thick and sticky.
[1]