Literature DB >> 1423511

Species differences in the immunoreactive patterns of calcitonin gene-related peptide in the pancreas.

C Sternini1, R De Giorgio, K Anderson, P C Watt, F C Brunicardi, A L Widdison, H Wong, H A Reber, J H Walsh, V L Go.   

Abstract

In the pancreas, calcitonin gene-related peptide (CGRP) immunoreactivity has been described in nerve fibers and in distinct types of islet cells. This unique, apparently species-specific cell-type expression prompted the present investigation to clarify further the pattern of CGRP immunoreactivity in different mammalian species (i.e., different strains of rats, mice, guinea pigs, rabbits, cats, dogs, pigs, and humans) commonly used for functional and anatomical studies of the pancreas by means of immunohistochemistry using three different CGRP antibodies. In each species, CGRP-immunoreactive neurites innervate the exocrine and endocrine compartments, the vasculature, and the intrapancreatic ganglia, where they form dense networks encircling unstained cell bodies. The only exception is the pig pancreas, where the islets appear to be devoid of immunoreactive fibers. The overall density of immunoreactive pancreatic axons in different species is as follows: rat, mouse, and rabbit greater than guinea pig greater than or equal to pig and cat much greater than dog and human. CGRP-immunoreactive endocrine cells appear to be restricted to the rat pancreas, where they form a subpopulation of somatostatin-containing D cells. In contrast, in mouse, guinea pig, cat, dog, and human pancreas, a homogeneous staining of the core of the islets, where insulin-producing B cells are located, was visualized in sections incubated with the rabbit CGRP antiserum at 4 degrees C, but not at 37 degrees C (an incubation temperature that does not affect the islet cell staining in the rat nor the fiber labeling in any species). Furthermore, the staining of islet B cells was not reproducible with all the CGRP antibodies used, all of which comparably stain nerve fibers in each species, and islet D cells in the rat. Immunoreactive islet cells were not visualized in pig and rabbit pancreas. These results are consistent with the hypothesis that the expression of CGRP in nerve fibers is a common feature of mammalian pancreas, whereas its expression in endocrine cells appears to be restricted to the D cells of the rat pancreas.

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Year:  1992        PMID: 1423511     DOI: 10.1007/bf00353900

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  50 in total

1.  Dual effects of calcitonin gene-related peptide on insulin secretion in the perfused dog pancreas.

Authors:  K Hermansen; B Ahrén
Journal:  Regul Pept       Date:  1990-01

Review 2.  Calcitonin gene-related peptide: novel neuropeptide.

Authors:  E C Goodman; L L Iversen
Journal:  Life Sci       Date:  1986-06-16       Impact factor: 5.037

3.  Purification and characterization of a peptide from amyloid-rich pancreases of type 2 diabetic patients.

Authors:  G J Cooper; A C Willis; A Clark; R C Turner; R B Sim; K B Reid
Journal:  Proc Natl Acad Sci U S A       Date:  1987-12       Impact factor: 11.205

4.  Calcitonin gene-related peptide inhibits exocrine secretion from the rat pancreas by a neurally mediated mechanism.

Authors:  N W Bunnett; S J Mulvihill; H T Debas
Journal:  Exp Physiol       Date:  1991-01       Impact factor: 2.969

5.  Guinea pig pancreatic ganglia: projections, transmitter content, and the type-specific localization of monoamine oxidase.

Authors:  A L Kirchgessner; J E Pintar
Journal:  J Comp Neurol       Date:  1991-03-22       Impact factor: 3.215

6.  Inhibition of gastric and pancreatic secretion in dogs by CGRP: role of somatostatin.

Authors:  W S Helton; M M Mulholland; N W Bunnett; H T Debas
Journal:  Am J Physiol       Date:  1989-04

7.  Calcitonin gene-related peptide: occurrence in pancreatic islets in the mouse and the rat and inhibition of insulin secretion in the mouse.

Authors:  M Pettersson; B Ahrén; G Böttcher; F Sundler
Journal:  Endocrinology       Date:  1986-08       Impact factor: 4.736

8.  Effect of calcitonin and calcitonin gene-related peptide on pancreatic functions in man.

Authors:  C Beglinger; E Koehler; W Born; J A Fischer; U Keller; L E Hanssen; K Gyr
Journal:  Gut       Date:  1988-02       Impact factor: 23.059

9.  Effect of calcitonin gene-related peptide on glucose and gastric inhibitory polypeptide-stimulated insulin release from cultured newborn and adult rat islet cells.

Authors:  J Ishizuka; G H Greeley; C W Cooper; J C Thompson
Journal:  Regul Pept       Date:  1988-01

10.  Human and rat alpha-CGRP but not calcitonin cause mesenteric vasodilatation in rats.

Authors:  I Marshall; S J Al-Kazwini; J J Holman; R K Craig
Journal:  Eur J Pharmacol       Date:  1986-04-16       Impact factor: 4.432

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  6 in total

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Authors:  F C Brunicardi; D M Shavelle; D K Andersen
Journal:  Int J Pancreatol       Date:  1995-12

2.  The role of CGRP and afferent nerves in the modulation of pancreatic enzyme secretion in the rat.

Authors:  J Jaworek; S J Konturek; A Szlachcic
Journal:  Int J Pancreatol       Date:  1997-10

3.  Endogenous opioids inhibit early-stage pancreatic pain in a mouse model of pancreatic cancer.

Authors:  Molly A Sevcik; Beth M Jonas; Theodore H Lindsay; Kyle G Halvorson; Joseph R Ghilardi; Michael A Kuskowski; Pinku Mukherjee; John E Maggio; Patrick W Mantyh
Journal:  Gastroenterology       Date:  2006-09       Impact factor: 22.682

4.  Monoclonal therapy against calcitonin gene-related peptide lowers hyperglycemia and adiposity in type 2 diabetes mouse models.

Authors:  Jonathan Halloran; Alexandre Lalande; Mandy Zang; Harshita Chodavarapu; Céline E Riera
Journal:  Metabol Open       Date:  2020-10-08

Review 5.  Pain and pain generation in pancreatic cancer.

Authors:  Fabio F di Mola; Pierluigi di Sebastiano
Journal:  Langenbecks Arch Surg       Date:  2008-01-12       Impact factor: 3.445

6.  Islet amyloid polypeptide gene expression in the endocrine pancreas of the rat: a combined in situ hybridization and immunocytochemical study.

Authors:  H Mulder; A C Lindh; F Sundler
Journal:  Cell Tissue Res       Date:  1993-12       Impact factor: 5.249

  6 in total

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