CFTR is an apically resident ion channel whose activity is regulated by the
activation of the cAMP mediated second messenger cascade. As depicted in t
extbooks, the cAMP mediated signaling cascade appears deceptively simple, y
et, our growing understanding of this pathway shows it to be much more comp
licated and finely tuned than originally thought. The intent of this review
is to evaluate our current understanding of the cAMP mediated signaling as
it relates to the secretion of mucin and chloride, two compounds whose reg
ulated secretion is altered in cystic fibrosis.