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. 1972 Jun 1;53(3):642–653. doi: 10.1083/jcb.53.3.642

THE BIOSYNTHESIS, INTRACELLULAR TRANSPORT, AND PACKAGING OF MELANOCYTE-STIMULATING PEPTIDES IN THE AMPHIBIAN PARS INTERMEDIA

C R Hopkins 1
PMCID: PMC2108773  PMID: 5028257

Abstract

Experiments in which glycine-3H has been introduced into excised neurointermediate lobes of Xenopus laevis incubated in a modified Krebs-Ringer bicarbonate medium have shown that ∼ 50% of the incorporated radioactivity is present in small peptides which have an electrophoretic mobility characteristic of the melanocyte-stimulating (MSH) peptides shown to be elaborated within the tissue. Based on these results and the demonstration that a discrete ∼ 7 min pulse of the label can be introduced into the tissue, electron microscope radioautography has been employed to follow the subcellular events concerned with the synthesis, intracellular transport, and packaging of the labeled secretory product. Together, these studies indicate that the newly synthesized material arises in peptide form, rather than as part of a larger prohormone molecule, on the ribosomes of the rough endoplasmic reticulum within the parenchymal cells of the intermediate portion of the lobe. A proportion is then incorporated into and remains for an extended period within the intracisternal granules which are a feature of the rough endoplasmic reticulum within these cells in vitro Most (∼ 60%) of the labeled secretory product, however, is transferred to the Golgi complex within 30 min and, within a further 10 min, becomes packaged into small (∼ 200 mµ) electron-opaque secretory granules. It is probable that under the conditions employed these granules represent the final intracellular location of secretory product before it is released

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Selected References

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  1. BARGMANN W., KNOOP A. [On the morphological relationships of the neurosecretory diencephalon system to the intermediate lobes of the hypophysis (light- and electron microscopic studies)]. Z Zellforsch Mikrosk Anat. 1960;52:256–277. [PubMed] [Google Scholar]
  2. BURGERS A. C. Melanophore-stimulating hormones in vertebrates. Ann N Y Acad Sci. 1963 Feb 15;100:669–677. doi: 10.1111/j.1749-6632.1963.tb42923.x. [DOI] [PubMed] [Google Scholar]
  3. CONTOPOULOS A. N., SIMPSON M. E., KONEFF A. A. Pituitary function in the thyroidectomized rat. Endocrinology. 1958 Nov;63(5):642–653. doi: 10.1210/endo-63-5-642. [DOI] [PubMed] [Google Scholar]
  4. ENNIS H. L., LUBIN M. CYCLOHEXIMIDE: ASPECTS OF INHIBITION OF PROTEIN SYNTHESIS IN MAMMALIAN CELLS. Science. 1964 Dec 11;146(3650):1474–1476. doi: 10.1126/science.146.3650.1474. [DOI] [PubMed] [Google Scholar]
  5. ETKIN W. Neurosecretory control of the pars intermedia. Gen Comp Endocrinol. 1962 Feb;2:161–169. doi: 10.1016/0016-6480(62)90036-9. [DOI] [PubMed] [Google Scholar]
  6. Hall T. C., Cocking E. C. High-efficiency liquid-scintillation counting of 14C-labelled material in aqueous solution and determination of specific activity of labelled proteins. Biochem J. 1965 Sep;96(3):626–633. doi: 10.1042/bj0960626. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Howell S. L., Kostianovsky M., Lacy P. E. Beta granule formation in isolated islets of langerhans: a study by electron microscopic radioautography. J Cell Biol. 1969 Sep;42(3):695–705. doi: 10.1083/jcb.42.3.695. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Jamieson J. D., Palade G. E. Intracellular transport of secretory proteins in the pancreatic exocrine cell. 3. Dissociation of intracellular transport from protein synthesis. J Cell Biol. 1968 Dec;39(3):580–588. doi: 10.1083/jcb.39.3.580. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Jamieson J. D., Palade G. E. Intracellular transport of secretory proteins in the pancreatic exocrine cell. I. Role of the peripheral elements of the Golgi complex. J Cell Biol. 1967 Aug;34(2):577–596. doi: 10.1083/jcb.34.2.577. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Jamieson J. D., Palade G. E. Synthesis, intracellular transport, and discharge of secretory proteins in stimulated pancreatic exocrine cells. J Cell Biol. 1971 Jul;50(1):135–158. doi: 10.1083/jcb.50.1.135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. McCann S. M., Porter J. C. Hypothalamic pituitary stimulating and inhibiting hormones. Physiol Rev. 1969 Apr;49(2):240–284. doi: 10.1152/physrev.1969.49.2.240. [DOI] [PubMed] [Google Scholar]
  12. Orci L., Lambert A. E., Kanazawa Y., Amherdt M., Rouiller C., Renold A. E. Morphological and biochemical studies of B cells of fetal rat endocrine pancreas in organ culture. Evidence for (pro) insulin biosynthesis. J Cell Biol. 1971 Sep;50(3):565–582. doi: 10.1083/jcb.50.3.565. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Palade G. E. Structure and function at the cellular level. JAMA. 1966 Nov 21;198(8):815–825. [PubMed] [Google Scholar]
  14. SALPETER M. M., BACHMANN L. AUTORADIOGRAPHY WITH THE ELECTRON MICROSCOPE. A PROCEDURE FOR IMPROVING RESOLUTION, SENSITIVITY, AND CONTRAST. J Cell Biol. 1964 Aug;22:469–477. doi: 10.1083/jcb.22.2.469. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Tixier-Vidal A., Gourdji D. Synthesis and renewal of proteins in duck anterior hypophysis in organ culture. J Cell Biol. 1970 Jul;46(1):130–136. doi: 10.1083/jcb.46.1.130. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. YOUNG B. A., FOSTER C. L., CAMERON E. SOME OBSERVATIONS ON THE ULTRASTRUCTURE OF THE ADENOHYPOPHYSIS OF THE RABBIT. J Endocrinol. 1965 Feb;31:279–287. doi: 10.1677/joe.0.0310279. [DOI] [PubMed] [Google Scholar]

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