Skip to main content
Log in

Regulation of secretory granule formation in chronically hypersecretory melanotrophs in the rat pituitary

  • Published:
Cell and Tissue Research Aims and scope Submit manuscript

Abstract

The formation of secretory granules in chronically hypersecretory melanotrophs in the rat pituitary was studied. Hypersecretion was induced by treatment with the dopamine antagonist haloperidol (1.5 mg/kg daily for 7 days), which releases the normal neural dopaminergic inhibition of secretion from the melanotroph. Morphometric analysis showed a 100% increase in the volume fraction of granular endoplasmic reticulum after haloperidol treatment, while the volume fractions of electron-dense granules, electron-lucent granules and the Golgi apparatus were unaltered. The mean diameter of the mature secretory granules was increased by 10%, indicating a 30% increase in mean granule volume. A similar increase in diameter was observed in condensing granules within the Golgi area. With earlier results on the effect of chronic inhibition the study shows that a main adaptive response of the melanotroph to altered secretory conditions is a change in the volume of the secretory granules, regulated by a mechanism that operates at an early stage of granule formation.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Bäck N (1989) The effect of bromocriptine on the intermediate lobe of the rat pituitary: an electron-microscopic, morphometric study. Cell Tissue Res 255:405–410

    Google Scholar 

  • Bäck N (1990) Effect of isoproterenol stimulation on the peripheral zone of intermediate lobe cells of the rat pituitary — preferential release of electron-lucent granules. Neuroendocrinology 52:328–331

    Google Scholar 

  • Bäck N, Rechardt L (1985) The effect of reserpine on the pars intermedia of the rat pituitary. An electron-microscopic, fluorescence-histochemical and immunohistochemical study. Cell Tissue Res 241:1–8

    Google Scholar 

  • Bertini LT, Kiss JZ (1991) Hypophysiotrophic neurons are capable of altering the ratio of co-packaged neurohormones. Neurosci 42:237–244

    Google Scholar 

  • Burgess TL, Kelly RB (1987) Constitutive and regulated secretion of proteins. Ann Rev Cell Biol 3:243–293

    Google Scholar 

  • Carr JA, Saland LC, Samora A, Benavidez S, Krobert K (1991) In vivo effects of serotonergic agents on alpha-melanocyte-stimulating hormone secretion. Neuroendocrinology 54:616–622

    Google Scholar 

  • Chanat E, Huttner WB (1991) Milieu-induced, selective aggregation of regulated secretory proteins in the trans-Golgi network. J Cell Biol 115:1505–1519

    Google Scholar 

  • Chen CLC, Dionne FT, Roberts JL (1983) Regulation of the proopiomelanocortin mRNA levels in rat pituitary by dopaminergic compounds. Proc Natl Acad Sci USA 80:2211–2215

    Google Scholar 

  • Childs GV, Unabia G, Ellison D (1986) Immunocytochemical studies on pituitary hormones with PAP, ABC, and immunogold techniques: evolution of technology to best fit the antigen. Am J Anat 175:307–330

    Google Scholar 

  • Chronwall BM, Hook GR, Millington WR (1988) Dopaminergic regulation of the biosynthetic activity of individual melanotropes in the rat pituitary intermediate lobe: a morphometric analysis by light and electron microscopy and in situ hybridization. Endocrinology 123:1992–2002

    Google Scholar 

  • Cote TE, Eskay RL, Frey EA, Grewe CW, Munemura M, Stoof JC, Tsuruta K, Kebabian JW (1982) Biochemical and physiological studies of the beta-adrenoreceptor and the D-2 dopamine receptor in the intermediate lobe of the rat pituitary gland: a review. Neuroendocrinology 35:217–224

    Google Scholar 

  • Eipper BA, Mains RE, Herbert E (1986) Peptides in the nervous system. Trends Neurosci 9:463–468

    Google Scholar 

  • Farquhar MG, Reid JJ, Daniell LW (1978) Intracellular transport and packaging of prolactin: a quantitative electron microscope autoradiographic study of mammotrophs dissociated from rat pituitaries. Endocrinology 102:296–311

    Google Scholar 

  • Gertz BJ, Contreras LN, McComb DJ, Kovacs K, Tyrrell JB, Dallman MF (1987) Chronic administration of corticotropin-releasing factor increases pituitary corticotroph number. Endocrinology 120:381–388

    Google Scholar 

  • Ham J, Smyth DG (1985) β-Endorphin processing in pituitary and brain is sensitive to haloperidol stimulation. Neuropeptides 5:497–500

    Google Scholar 

  • Höllt V, Haarmann I, Seizinger BR, Herz A (1982) Chronic haloperidol treatment increases the level of in vitro translatable messenger ribonucleic acid coding for the β-endorphin/adrenocorticotropin precursor proopiomelanocortin in the pars intermedia of the rat pituitary. Endocrinology 110:1885–1891

    Google Scholar 

  • Kelly RB (1991) Secretory granule and synaptic vesicle formation. Curr Opin Cell Biol 3:654–660

    Google Scholar 

  • Malagón MM, Garcia-Navarro S, Ruiz-Navarro A, Gracia-Navarro F (1989) Morphometric evaluation of subcellular changes induced by in vivo TRH treatment in the pituitary gland of Rana perezi: effects on prolactin and thyrotropic cells. Cell Tissue Res 256:391–398

    Google Scholar 

  • Milner GR, de Gasparo M, Kay R, Milner RDG (1979) Effects of glucose and amino acids on insulin, glucagon and zymogen granule size of foetal rat pancreas grown in organ culture. J Endocrinol 82:179–189

    Google Scholar 

  • Millington WR, Maiewski S, O'Donohue TL, Mueller GP (1985) Long-term haloperidol treatment elevates β-endorphin levels in the intermediate pituitary but not in rat brain. Neuropeptides 6:365–372

    Google Scholar 

  • Moriarty GC, Halmi NS (1972) Electron microscopic study of the adrenocorticotropin-producing cell with the use of unlabeled antibody and the soluble peroxidase-antiperoxidase complex. J Histochem Cytochem 20:590–603

    Google Scholar 

  • Orci L (1986) The morphology of proinsulin processing. Ann N Y Acad Sci 488:292–316

    Google Scholar 

  • Rambourg A, Clermont Y (1990) Three-dimensional electron microscopy: structure of the Golgi apparatus. Eur J Cell Biol 51:189–200

    Google Scholar 

  • Rambourg A, Clermont Y, Chrétien M, Olivier L (1992) Formation of secretory granules in the Golgi apparatus of prolactin cells in the rat pituitary gland: a stereoscopic study. Anat Rec 232:169–179

    Google Scholar 

  • Saland LC (1978) Effects of reserpine administration on the fine structure of the rat pars intermedia. Cell Tissue Res 194:115–123

    Google Scholar 

  • Saland LC, Ortiz E, Munger AT (1982) Effects of acute opiate-peptide administration on pro-opiomelanocortin cells of the intermediate lobe of the rat pituitary. Cell Tissue Res 225:217–222

    Google Scholar 

  • Saland LC, Reyes E, Ortiz E (1984) Naltrexone effects on pituitary intermediate lobe and median eminence. Neurochem Res 9:207–217

    Google Scholar 

  • Scammell JG, Burrage TG, Dannies PS (1986) Hormonal induction of secretory granules in a pituitary tumor cell line. Endocrinology 119:1543–1548

    Google Scholar 

  • Scmitt G, Stoeckel ME, Klein MJ, Porte A (1982) Effects of experimental hypo- or hyponatremia on the fine structure of the pars intermedia of the murine pituitary. A morphometric study. Cell Tissue Res 223:641–657

    Google Scholar 

  • Schnabel E, Mains RE, Farquhar MG (1989) Proteolytic processing of pro-ACTH/endorphin begins in the Golgi complex of pituitary corticotropes and AtT-20 cells. Mol Endocrinol 3:1223–1235

    Google Scholar 

  • Tanaka S, Nomizu M, Kurosumi K (1991) Intracellular site of proteolytic processing of pro-opiomelanocortin in melanotrophs and corticotrophs in rat pituitary. J Histochem Cytochem 39:809–821

    Google Scholar 

  • Tilders FJH, Berkenbosch F, Smelik PG (1985) Control of secretion of peptides related to adrenocorticotropin, melanocyte-stimulating hormone and endorphin. Front Horm Res 14:161–196

    Google Scholar 

  • Tixier-Vidal A, Farquhar MG (eds) (1975) The anterior pituitary. Academic Press, New York

    Google Scholar 

  • Tooze SA (1991) Biogenesis of secretory granules. Implications arising from the immature secretory granule in the regulated pathway of secretion. FEBS Lett 285:220–224

    Google Scholar 

  • Tooze SA, Huttner WB (1990) Cell-free protein sorting to the regulated and constitutive secretory pathways. Cell 60:837–847

    Google Scholar 

  • Tooze SA, Flatmark T, Tooze J, Huttner WB (1991) Characterization of the immature secretory granule, an intermediate in granule biogenesis. J Cell Biol 115:1491–1503

    Google Scholar 

  • Uylings HBM, Eden CG van, Hofman MA (1986) Morphometry of size/volume variables and comparison of their bivariate relations in the nervous system under different conditions. J Neurosci Meth 18:19–37

    Google Scholar 

  • Weibel ER (1979) Stereological methods, vol 1. Practical methods for biological morphometry. Academic Press, London

    Google Scholar 

  • Weintraub H, Abramovici A, Amichai D, Eldar T, Ben-Dor L, Pentchev PG, Hammel I (1992) Morphometric studies of pancreatic acinar granule formation in NCTR-Balb/c mice. J Cell Sci 102:141–147

    Google Scholar 

  • Ziegler B (1963) Licht- und elektronenmikroskopische Untersuchungen an Pars intermedia und Neurohypophyse der Ratte. Z Zellforsch 59:486–506

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Bäck, N., Soinila, S. Regulation of secretory granule formation in chronically hypersecretory melanotrophs in the rat pituitary. Cell Tissue Res 275, 339–344 (1994). https://doi.org/10.1007/BF00319432

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00319432

Key words

Navigation