ISSN:
0002-9106
Schlagwort(e):
Life and Medical Sciences
;
Cell & Developmental Biology
Quelle:
Wiley InterScience Backfile Collection 1832-2000
Thema:
Medizin
Notizen:
The distribution of cells displaying glucagonlike or gastric inhibitory polypeptide (GIP)-like immunoreactivity was examined in the pancreatic islets and gastrointestinal tracts of rats, dogs, and humans. A-cells in the pancreatic islets in all three species were stained by antisera having regional specificity for pancreatic-type glucagon, gut-type glucagon (glicentin), or GIP. Oxyntic A-cells of the gastric mucosa in dogs and humans also were stained comparably by these three antisera. In contrast, the K- and L-cells in the intestinal mucosa of those species were stained only by antisera capable of reacting with GIP or gut-type glucagon, respectively. Tests of antibody specificity showed that the GIP antiserum did not cross-react with either pancreaticor gut-type glucagon. Likewise, the glucagon antisera showed no cross-reactivity with GIP. Hence, these findings suggest that pancreatic and gastric A-cells contain a peptide with GIP-like immunoreactivity distinct from glucagon or glicentin per se. Although the exact basis of the GIP-like immunostaining of A-cells is unknown, it may be due to the presence of a glucagon precursor sharing certain amino-acid sequences with GIP. This hypothesis is consistent with several recent investigations showing that the processing of proglucagon molecules differs between the A- and L-cells.
Zusätzliches Material:
10 Ill.
Materialart:
Digitale Medien
URL:
http://dx.doi.org/10.1002/aja.1001680111
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