The structure of the oral mucosa has been extensively studied but its cell
physiology has been less well characterised. This study aimed to show the r
ange in variation in fluid phase endocytic capability in biopsies from diff
erent oral sites. Oral epithelial cells were obtained from both biopsies an
d single-cell suspensions obtained by brushing the oral cavity. Biopsies in
organ culture and single cells in suspension were incubated with fluoresce
nt microspheres of 0.02, 0.1 or 1.0 mu m diameter. Endocytosis of fluoresce
nt microspheres was quantitated by flow cytometry and visualised by confoca
l microscopy. Epithelial cells from all oral sites that were sampled intern
alised 0.02 mu m and 0.1 mu m but not 1.0 mu m microspheres, with no signif
icant differences observed between oral regions. Single cells from non-canc
er patients endocytosed significantly more 0.02 mu m microspheres than cell
s removed from patients with oral cancer. This model may be used to study i
ntegrated oral cell function both in health and disease.