Distribution of heat-stable enterotoxin/guanylin receptors in the intestinal tract of man and other mammals
- PMID: 8014132
- PMCID: PMC1260001
Distribution of heat-stable enterotoxin/guanylin receptors in the intestinal tract of man and other mammals
Abstract
The human intestinal tract, as well as that of several eutherian and metatherian mammals, was examined for the distribution of heat-stable enterotoxin (ST)/guanylin receptors. These receptors were confined to the intestinal epithelium lining the lumen and forming the intestinal glands throughout the length of both the small intestine and colon of all species examined. In man and most other mammalian species, there appeared to be a decrease in receptor density distally along the longitudinal axis of the small intestine. ST/guanylin receptors were not observed in other strata forming the gut wall. Along the vertical axis of the human small intestine (villus/crypt unit), as well as that of most other mammals, receptor density was greatest in enterocytes located near the base of villi and in those forming the proximal portion of the intestinal glands. ST/guanylin receptors were for the most part confined to the region of the plasmalemma forming the microvillus border. In the colon of man and the other species examined, receptor density was greatest in enterocytes forming the proximal region of the intestinal glands. Receptors were present in the intestinal epithelium lining the lumen of the colon, but generally were fewer in number. The distribution of cellular cGMP accumulation responses to E. coli ST and guanylin in the opossum (Didelphis virginiana) and raccoon (Procyon lotor) revealed that proximal small intestine had greater magnitudes of cGMP responses than did the distal small intestine. Proximal colon had greater cGMP responses than distal colon, which had no significant cGMP responses to either ST or guanylin.
Similar articles
-
Distribution of Escherichia coli heat-stable enterotoxin/guanylin/uroguanylin receptors in the avian intestinal tract.Acta Anat (Basel). 1995;153(3):210-9. doi: 10.1159/000147735. Acta Anat (Basel). 1995. PMID: 8984830
-
Guanylyl cyclase receptors and guanylin-like peptides in reptilian intestine.Gen Comp Endocrinol. 1997 Aug;107(2):229-39. doi: 10.1006/gcen.1997.6921. Gen Comp Endocrinol. 1997. PMID: 9245531
-
Signal transduction pathways via guanylin and uroguanylin in stomach and intestine.Am J Physiol. 1997 Jul;273(1 Pt 1):G93-105. doi: 10.1152/ajpgi.1997.273.1.G93. Am J Physiol. 1997. PMID: 9252514
-
Enterotoxin/guanylin receptor type guanylyl cyclases in non-mammalian vertebrates.Zoolog Sci. 2005 May;22(5):501-9. doi: 10.2108/zsj.22.501. Zoolog Sci. 2005. PMID: 15930822 Review.
-
Uroguanylin and guanylin peptides: pharmacology and experimental therapeutics.Pharmacol Ther. 2004 Nov;104(2):137-62. doi: 10.1016/j.pharmthera.2004.08.007. Pharmacol Ther. 2004. PMID: 15518884 Review.
Cited by
-
Mechanisms of actions of guanylin peptides in the kidney.Pflugers Arch. 2005 Aug;450(5):283-91. doi: 10.1007/s00424-005-1464-9. Epub 2005 Jun 11. Pflugers Arch. 2005. PMID: 15952032 Review.
-
Enteric bacterial toxins: mechanisms of action and linkage to intestinal secretion.Microbiol Rev. 1996 Mar;60(1):167-215. doi: 10.1128/mr.60.1.167-215.1996. Microbiol Rev. 1996. PMID: 8852900 Free PMC article. Review. No abstract available.
-
Regulation of intestinal uroguanylin/guanylin receptor-mediated responses by mucosal acidity.Proc Natl Acad Sci U S A. 1997 Mar 18;94(6):2705-10. doi: 10.1073/pnas.94.6.2705. Proc Natl Acad Sci U S A. 1997. PMID: 9122260 Free PMC article.
-
Guanylyl cyclase C agonists regulate progression through the cell cycle of human colon carcinoma cells.Proc Natl Acad Sci U S A. 2001 Jul 3;98(14):7846-51. doi: 10.1073/pnas.141124698. Proc Natl Acad Sci U S A. 2001. PMID: 11438734 Free PMC article.
-
Novel GUCY2C variant causing familial diarrhea in a Mennonite kindred and a potential therapeutic approach.Am J Med Genet A. 2021 Jul;185(7):2046-2055. doi: 10.1002/ajmg.a.62207. Epub 2021 May 5. Am J Med Genet A. 2021. PMID: 33949097 Free PMC article.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources