There is considerable debate about whether the mucous neck cell (MNC) in th
e mucosa of the gastric corpus is merely a transit cell population, interme
diate between gastric stem cells and the differentiated zymogenic (chief or
peptic) cell lineages, or has distinct functions of its own. To cast light
on these possibilities, the secretory phenotype of the MNC has been examin
ed. Archival gastric body samples from non-ulcer dyspepsia biopsies and gas
trectomies performed for peptic ulcer disease were stained with antibodies
to the trefoil peptides TFF1/pS2 and TFF2/SP, pancreatic secretory trypsin
inhibitor (PSTI), epidermal growth factor (EGF) and its receptor (EGFR), an
d to the MUC1 gene product-HMFG2, Human MNCs express PSTI, TFF1/pS2, TFF2/S
P, and EGF proteins, while rat MNCs express TFF2/SP; the mucin contained in
the MNCs is diastase/periodic acid Schiff (D/PAS)-positive and stains with
human milk fat globulin (HMFG2), The canaliculi but not the cytoplasm of a
djacent parietal cells were also decorated focally by D/PAS, by HMFG2, and
by antibodies to TFF2/SP and TFF1/pS2, These findings favour the hypothesis
that MNCs have a defined phenotype and are thus a separate and distinct ce
ll lineage, secreting a number of luminally-active peptides which protect t
he gastric mucosa, and in particular the adjacent parietal cells, from the
effects of secreted gastric acid. Moreover, a considerable degree of simila
rity in secretory profile is noted between MNCs and the so-called 'reparati
ve lineages' in the gut-the ulcer-associated cell lineage (UACL) and hyperp
lastic polyp epithelium. If, on the other hand, the MNCs are indeed a trans
it population differentiating into zymogenic or peptic cells, then it is cl
ear that having differentiated into one secretory phenotype producing a ran
ge of peptides, the MNC then proceeds to differentiate into a cell with a t
otally different secretory phenotype, a phenomenon unique in gastrointestin
al cell lineage relationships. Copyright (C) 1999 John Wiley & Sons, Ltd.