P. Webster et al., SUBCELLULAR-LOCALIZATION OF CFTR TO ENDOSOMES IN A DUCTAL EPITHELIUM, The American journal of physiology, 267(2), 1994, pp. 30000340-30000348
Plasma membrane chloride transport by the cystic fibrosis transmembran
e conductance regulator (CFTR) may be regulated by cellular processes
that affect the cycling of CFTR with the plasma membrane. Testing this
hypothesis requires cytochemical evidence for the presence of a subce
llular compartment of CFTR. In this study, the subcellular distributio
n of CFTR in a normal epithelial cell population was characterized usi
ng immunofluorescence and immunoelectron microscopy. Two anti-CFTR ant
ibodies, raised against different epitopes of the CFTR molecule, speci
fically labeled the apical pole of striated duct epithelial cells in t
issue sections of rat submandibular gland. By use of electron microsco
py, the CFTR immunoreactivity was associated with the apical plasma me
mbrane and the membranes of many subapical vesicles. In this preparati
on, some of the CFTR-labeled vesicles were also labeled with antibodie
s against transferrin receptor and rab4, two markers of early endosome
s and receptor-mediated endocytosis. These observations provide direct
cytochemical evidence for the existence of peripherally located CFTR-
expressing endosomes and support the hypothesis that membrane recyclin
g may contribute to CFTR function.