Relationships of endocrine cells to each other and to other cell types in the human gastric fundus and corpus.


Journal

Cell and tissue research
ISSN: 1432-0878
Titre abrégé: Cell Tissue Res
Pays: Germany
ID NLM: 0417625

Informations de publication

Date de publication:
Apr 2019
Historique:
received: 30 07 2018
accepted: 01 11 2018
pubmed: 24 11 2018
medline: 20 8 2019
entrez: 24 11 2018
Statut: ppublish

Résumé

Gastric endocrine cell hormones contribute to the control of the stomach and to signalling to the brain. In other gut regions, enteroendocrine cells (EECs) exhibit extensive patterns of colocalisation of hormones. In the current study, we characterise EECs in the human gastric fundus and corpus. We utilise immunohistochemistry to investigate EECs with antibodies to ghrelin, serotonin (5-HT), somatostatin, peptide YY (PYY), glucagon-like peptide 1, calbindin, gastrin and pancreastatin, the latter as a marker of enterochromaffin-like (ECL) cells. EECs were mainly located in regions of the gastric glands populated by parietal cells. Gastrin cells were absent and PYY cells were very rare. Except for about 25% of 5-HT cells being a subpopulation of ECL cells marked by pancreastatin, colocalisation of hormones in gastric EECs was infrequent. Ghrelin cells were distributed throughout the fundus and corpus; most were basally located in the glands, often very close to parietal cells and were closed cells i.e., not in contact with the lumen. A small proportion had long processes located close to the base of the mucosal epithelium. The 5-HT cells were of at least three types: small, round, closed cells; cells with multiple, often very long, processes; and a subgroup of ECL cells. Processes were in contact with their surrounding cells, including parietal cells. Mast cells had very weak or no 5-HT immunoreactivity. Somatostatin cells were a closed type with long processes. In conclusion, four major chemically defined EEC types occurred in the human oxyntic mucosa. Within each group were cells with distinct morphologies and relationships to other mucosal cells.

Identifiants

pubmed: 30467709
doi: 10.1007/s00441-018-2957-0
pii: 10.1007/s00441-018-2957-0
pmc: PMC6451671
mid: NIHMS1524846
doi:

Substances chimiques

Gastrointestinal Hormones 0

Types de publication

Journal Article

Langues

eng

Pagination

37-49

Subventions

Organisme : NIH HHS
ID : OT2 OD023847
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK057236
Pays : United States
Organisme : National Institutes of Health
ID : OT2OD023847

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Auteurs

Josiane Fakhry (J)

Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia.

Martin J Stebbing (MJ)

Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia.
Florey Institute of Neuroscience and Mental Health, Parkville, VIC, 3010, Australia.

Billie Hunne (B)

Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia.

Yulia Bayguinov (Y)

Department of Physiology and Cell Biology, Reno School of Medicine, University of Nevada, Reno, NV, 89557, USA.

Sean M Ward (SM)

Department of Physiology and Cell Biology, Reno School of Medicine, University of Nevada, Reno, NV, 89557, USA.

Kent C Sasse (KC)

School of Medicine, Universiity of Nevada, Reno, NV, 89557, USA.
Renown Regional Medical Center, Reno, NV, 89502, USA.

Brid Callaghan (B)

Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia.

Rachel M McQuade (RM)

Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia.
Florey Institute of Neuroscience and Mental Health, Parkville, VIC, 3010, Australia.

John B Furness (JB)

Department of Anatomy and Neuroscience, University of Melbourne, Parkville, VIC, 3010, Australia. j.furness@unimelb.edu.au.
Florey Institute of Neuroscience and Mental Health, Parkville, VIC, 3010, Australia. j.furness@unimelb.edu.au.

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