Gastric endocrine cells: gene expression, processing, and targeting of active products
G. J. Dockray, A. Varro and R. Dimaline Physiological Laboratory, University of Liverpool, United Kingdom. Endocrine cells of the gastric epithelium secrete biologically active peptides and small messenger molecules such as histamine, serotonin, and gamma-aminobutyric acid. The secretory products ma...
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Veröffentlicht in: | Physiological reviews 1996-07, Vol.76 (3), p.767-798 |
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Zusammenfassung: | G. J. Dockray, A. Varro and R. Dimaline
Physiological Laboratory, University of Liverpool, United Kingdom.
Endocrine cells of the gastric epithelium secrete biologically active
peptides and small messenger molecules such as histamine, serotonin, and
gamma-aminobutyric acid. The secretory products may act locally (paracrine
or autocrine effects) or at distant targets after delivery in the
circulation (hormonal effects). the contents of the gastric lumen control
both secretion of gastric endocrine cells and the expression of genes
involved in the synthesis of their active secretory products; in some
cases, gene regulation may occur over periods as short as that required for
digestion of a single meal. The conversion of inactive peptide precursors
to their active forms takes place during transit along the secretory
pathway and is only completed after sequestration in secretory granules.
the processing of the gastrin precursor provides a useful model for
studying prohormone processing. Generation of the well-known amidated
gastrins requires prohormone cleavage and COOH-terminal amidation; the
products stimulate acid secretion and mucosal growth. However, recent work
indicates that biosynthetic intermediates that do not stimulate acid
secretion may nevertheless act at a novel receptor to stimulate growth, so
that control of prohormone processing determines which of two alternative
types of biologically active peptide is released by gastrin cells. Gastric
endocrine cells also have the capacity to accumulate small messenger
molecules in secretory vesicles, via proton exchangers. Recent work
indicates physiological regulation of the expression of genes encoding
cytosolic enzymes such as histidine decarboxylase, which converts histidine
to histamine, and of secretory granule transporters such as vesicular
monoamine transporter type 2, which concentrates amines in secretory
vesicles. Together these findings suggest that modulation of regulatory
peptide and amine biosynthesis in gastric endocrine cells constitutes a
primary response of the stomach to the arrival of a meal. |
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ISSN: | 0031-9333 1522-1210 |
DOI: | 10.1152/physrev.1996.76.3.767 |