The mucous neck cell in the human gastric corpus: A distinctive, functional cell lineage

Citation
Am. Hanby et al., The mucous neck cell in the human gastric corpus: A distinctive, functional cell lineage, J PATHOLOGY, 187(3), 1999, pp. 331-337
Citations number
36
Categorie Soggetti
Research/Laboratory Medicine & Medical Tecnology","Medical Research Diagnosis & Treatment
Journal title
JOURNAL OF PATHOLOGY
ISSN journal
00223417 → ACNP
Volume
187
Issue
3
Year of publication
1999
Pages
331 - 337
Database
ISI
SICI code
0022-3417(199902)187:3<331:TMNCIT>2.0.ZU;2-Z
Abstract
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.