Abstract
In the North American opossum, heat-stable specific binding sites for E. coli enterotoxin are observed (i) in epithelial cells lining the small intestine, colon, gall bladder, cystic duct, common bile duct and trachea, and (ii) in epithelial cells forming the duodenal (Brunner's) glands, liver, kidneys (metanephros, mesonephros) and testis, as demonstrated by autoradiography. Enterotoxin-specific binding sites in the intestinal tract are only found in intestinal epithelial cells with the highest concentration in the microvillus border. Enterotoxin-specific binding sites also occur in epithelial cells comprising the secretory tubules and ducts of the duodenal glands. In the kidneys (metanephros and mesonephros), enterotoxin-specific binding sites are confirmed primarily to the proximal tubules, whereas in the testis they are localized in seminiferous tubules. In the liver, enterotoxin-specific binding sites are confined primarily to hepatocytes. E. coli enterotoxin caused a 7-fold increase of cGMP in the liver and a 30-fold increase in the duodenal glands. The liver responded in about half of the animals studied, whereas the duodenal glands gave a consistent response in each case. Likewise, the duodenal glands consistently showed strong labelling for 125I-enterotoxin, whereas receptor labelling of hepatocytes was inconsistent in nearly half the incubations and corresponds to the observed cGMP measurements.
MeSH Terms
Animals
Autoradiography
Enterotoxins/metabolism
Epithelial Cells
Epithelium/metabolism,ultrastructure
Escherichia coli
Guanylate Cyclase
Iodine Radioisotopes
Male
Opossums/metabolism
Receptors, Cell Surface/metabolism
Receptors, Enterotoxin
Receptors, Guanylate Cyclase-Coupled
Receptors, Peptide
Tissue Distribution
Chemicals
Enterotoxins
Iodine Radioisotopes
Receptors, Cell Surface
Receptors, Peptide
Guanylate Cyclase
Receptors, Enterotoxin
Receptors, Guanylate Cyclase-Coupled
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Krause W J
Department of Anatomy, University of Missouri School of Medicine, Columbia 65212.
Freeman R H
Fort L R
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