Cytokeratin (CK) 20 is a low molecular-weight intermediate filament reporte
dly expressed only by benign and malignant gastrointestinal epithelium, uro
thelium and Merkel cells. The main aims here were to map its expression in
normal oral mucosa of humans and other mammals, and to determine whether it
was expressed by abnormal human oral epithelium. Salivary and odontogenic
epithelium were also analysed. An immunoperoxidase method was used on wax-e
mbedded and cryostat sections. In addition, double-labelling experiments we
re undertaken to determine the association between CK 20 expression and tha
t of CK 8/18 or S100 protein. Normal human oral mucosa from four sites, tog
ether with abdominal skin, was studied in autopsy samples from 32 individua
ls. CK 20-positive, basally situated, round or angular cells, consistent wi
th Merkel cells, were recorded in 24/32 (75.0%) samples of mandibular gingi
va, 25/32 (78.1%) samples of hard palate, 7/32 (21.9%) samples of buccal mu
cosa, 0/32 samples of lateral border of tongue, and 2/32 (6.3%) samples of
abdominal skin. Double-labelling showed that all CK 20-positive Merkel cell
s also expressed CK 8/18 and S100. The only other cells to express CK 20 we
re human taste buds. There was no expression by dysplastic or invasive oral
epithelium from biopsy samples. Colonic mucosa showed luminal-cell positiv
ity in man, marmoset, ferret, rabbit and guinea-pig, but oral mucosa was un
iversally negative in non-human species. It is concluded that in oral mucos
a CK 20 is a specific marker of Merkel cells and taste buds, that Merkel ce
lls are more frequently present in keratinized than non-keratinized oral mu
cosa, that CK 20-positive Merkel cells are also S100-positive, that there m
ay be interspecies variations in CK 20 polypeptide composition and that, by
contrast to urothelium, CK 20 has no value in the diagnosis of oral epithe
lial dysplasia. (C) 2000 Elsevier Science Ltd. All rights reserved.