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. 1975 Mar 1;64(3):724–733. doi: 10.1083/jcb.64.3.724

Caerulein secretion by dermal glands in xenopus laevis

GJ Dockray, CR Hopkins
PMCID: PMC2109542  PMID: 1150750

Abstract

Since gastrin and its related peptides are secreted by a minority population of widely dispersed cells in mamamalian tissues it has, in the past, been difficult to study the subcellular aspects of their secretion. From published reports (1, 2) it seemed possible that a satisfactory system for such studies might be provided by the skin of certain amphibians such as Xenopus laevis since in these tissues high concentrations of peptides such as caerulein exist, and there is some indication (3) that this, or a similar gastrin-like peptide, may be a dermal gland secretory product. We have therefore explored this possibility by studying the structure, secretory process, and secretory product of the most prominent non mucous type of gland in the skin of X. laevis. These studies clearly demonstrate that most, if not all, of the caerulein in which the skin is contained in secretion granules within the dermal glands and that its release can be specifically evoked by adrenergic stimulation. The release process by a holocrine mechanism expels all of the stored secretion onto the skin surface and thus for biosynthetic studies it should now be possible to synchronize the processes which lead to the replenishment of the peptide.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Anastasi A., Bertaccini G., Cei J. M., De Caro G., Erspamer V., Impicciatore M., Roseghini M. Presence of caerulein in extracts of the skin of Leptodactylus pentadactylus labyrinthicus and of Xenopus laevis. Br J Pharmacol. 1970 Jan;38(1):221–228. doi: 10.1111/j.1476-5381.1970.tb10351.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Anastasi A., Erspamer V., Endean R. Isolation and amino acid sequence of caerulein, the active decapeptide of the skin of hyla caerulea. Arch Biochem Biophys. 1968 Apr;125(1):57–68. doi: 10.1016/0003-9861(68)90638-3. [DOI] [PubMed] [Google Scholar]
  3. BASTIAN J. W., ZARROW M. X. Stimulation of the secretory glands of the skin of the South African frog (Xenopus laevis). Endocrinology. 1954 Jan;54(1):116–117. doi: 10.1210/endo-54-1-116. [DOI] [PubMed] [Google Scholar]
  4. Bertaccini G., De Caro G., Endean R., Erspamer V., Impicciatore M. The actions of caerulein on the smooth muscle of the gastrointestinal tract and the gall bladder. Br J Pharmacol. 1968 Oct;34(2):291–310. doi: 10.1111/j.1476-5381.1968.tb07052.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Dockray G. J. The action of gastrin and cholecystokinin-related peptides on pancreatic secretion in the rat. Q J Exp Physiol Cogn Med Sci. 1973 Apr;58(2):163–169. [PubMed] [Google Scholar]
  6. Dockray G. J. The action of scretin, cholecystokinin-pancreozymin and caerulein on pancreatic secretion in the rat. J Physiol. 1972 Sep;225(3):679–692. doi: 10.1113/jphysiol.1972.sp009963. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Farquhar M. G., Palade G. E. Cell junctions in amphibian skin. J Cell Biol. 1965 Jul;26(1):263–291. doi: 10.1083/jcb.26.1.263. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Ireland M. P. Effects of arginine vasotocin on sodium and potassium metabolism in Xenopus laevis after skin gland stimulation and sympathetic blockade. Comp Biochem Physiol A Comp Physiol. 1973 Feb 1;44(2):487–493. doi: 10.1016/0300-9629(73)90501-x. [DOI] [PubMed] [Google Scholar]
  9. LANGER E., HUHN S. Der submikroskopische Bau der Myoepithelzelle. Z Zellforsch Mikrosk Anat. 1958;47(5):507–516. [PubMed] [Google Scholar]
  10. LUFT J. H. Improvements in epoxy resin embedding methods. J Biophys Biochem Cytol. 1961 Feb;9:409–414. doi: 10.1083/jcb.9.2.409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ljungberg S. Biological assay of cholecystokinin in guinea-pig gall-bladder in situ. Acta Pharm Suec. 1969 Dec;6(6):599–606. [PubMed] [Google Scholar]
  12. Ondetti M. A., Rubin B., Engel S. L., Pluscec J., Sheehan J. T. Cholecystokinin-pancreozymin: recent developments. Am J Dig Dis. 1970 Feb;15(2):149–156. doi: 10.1007/BF02235646. [DOI] [PubMed] [Google Scholar]
  13. Polak J. M., Pearse A. G. Anti-gastrin immunofluorescence in the skin of Hyla crepitans and the cytochemistry of the cells involved. Experientia. 1970 Mar 15;26(3):288–289. doi: 10.1007/BF01900100. [DOI] [PubMed] [Google Scholar]

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