Skip to main content
Log in

Immunocytochemical effects of thyroxine stimulation on the adenohypophysis of dwarf (dw) mutant mice

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

Abstract

The effects of dietary thyroxine on the immunoreactivity of cells in the pars distalis of the adenohypophysis in dwarf (dw/dw) mice were determined by ultrastructural immunocytochemistry. In nontreated dwarfs only adrenocorticotropic hormone (ACTH) cells and luteinizing hormone (LH) cells showed positive reactions to their respective antibodies, whereas no cells showed immunoreactivity to antibodies to growth hormone (GH), thyroid-stimulating hormone (TSH), or prolactin (Prl). In dwarfs supplemented postnatally with dietary thyroxine for 9 wks, the treatment failed to produced immunoreactive GH, TSH or Prl cells. However, LH cells became more prominent and fully developed, with denser concentrations of immunoreactive particles overlying the secretory granules than occurred in nontreated dwarfs. In thyroxine-treated dwarfs, ACTH cells were similar in ultrastructural features and immunoreactivity to those in nontreated dwarfs.

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

  • Allaerts W, Carmeliet P, Denef C (1990) New perspectives in the function of pituitary folliculo-stellate cells. Mol Cell Endocrinol 71:73–81

    Google Scholar 

  • Baker BL, Gross DS (1978) Cytology and distribution of secretory cell types in the mouse hypophysis as demonstrated with immunocytochemistry. Am J Anat 153:193–216

    Google Scholar 

  • Bartke A (1965) The response of two types of dwarf mice to growth hormone, thyrotropin, and thyroxine. Gen Comp Endocrinol 5:418–426

    Google Scholar 

  • Bartke A (1971) The maintenance of gestation and the initiation of lactation in the mouse in the absence of pituitary prolactin. J Reprod Fert 27:121–124

    Google Scholar 

  • Bartke A, Goldman BD, Bex F, Dalterio S (1977) Effects of prolactin (PRL) on pituitary and testicular function in mice with hereditary Prl deficiency. Endocrinology 101:1760–1766

    Google Scholar 

  • Bartke A, Parkening TA, Collins TJ, Amador AG (1987) Treatment with thyroxine induces persistent elevation of plasma gonadotropin levels in genetically hypthyroid Snell dwarf mice. Neuroendocrinology 9:85–92

    Google Scholar 

  • Cheng TC, Beamer WG, Phillips JA III, Bartke A, Mallonee RL (1983) Etiology of growth hormone deficiency in Little, Ames, and Snell dwarf mice. Endocrinology 113:1669–1678

    Google Scholar 

  • Eicher EM, Beamer WG (1980) New mouse dw allele: genetic location and effects on lifespan and growth hormone levels. J Hered 71:187–190

    Google Scholar 

  • Elftman H, Wegelius O (1959) Anterior pituitary cytology of the dwarf mouse. Anat Rec 135:43–47

    Google Scholar 

  • Evans RM, Birnberg NC, Rosenfeld MG (1982) Glucocorticoid and thyroid hormones transcriptionally regulate growth hormone gene expression. Proc Natl Acad Sci USA 79:7659–7663

    Google Scholar 

  • Lewis UJ (1967) Growth hormone of normal and dwarf mice. Endocrinol Memoirs 15:179–191

    Google Scholar 

  • Li S, III Crenshaw EB, Rawson EJ, Simmons DM, Swanson LW, Rosenfeld MG (1990) Dwarf locus mutants lacking three pituitary cell types result from mutations in the POU-domain gene pit-1. Nature 347:528–533

    Google Scholar 

  • Marshak A (1938) Gonadotropic hormones in the hereditary dwarf mouse. Proc Soc Exp Biol Med 38:226–228

    Google Scholar 

  • Martial JA, Seeburg PH, Guenzi D, Goodman HM, Baxter JD (1977a) Regulation of growth hormone gene expression: synergistic effects of thyroid and glucocorticoid hormones. Proc Natl Acad Sci USA 74:4293–4295

    Google Scholar 

  • Martial JA, Baxter JD, Goodman HM, Seeburg PH (1977b) Regulation of growth hormone messenger RNA by thyroid and glucocorticoid hormones. Proc Natl Acad Sci USA 74:1816–1820

    Google Scholar 

  • Nyborg JK, Nguyen AP, Spindler SR (1985) Cyclic regulation of growth hormone gene transcription in vivo and in vitro. Endocrinology 116:2361–2365

    Google Scholar 

  • Parks JS, Herd JE, Wurzel JM, Martial JA(1982) Structural analysis of rodent growth hormone genes: application to genetic forms of hypotituitarism. Endocrinology 110:1672–1675

    Google Scholar 

  • Phillips JA III, Beamer WG, Bartke A (1982) Analysis of growth hormone genes in mice with genetic defects of growth hormone expression. J Endocrinol 92:405–407

    Google Scholar 

  • Roti E, Christianson D, Harris ARC, Braverman LE, Vagenakis AG (1978) “Short” loop feedback regulation of hypothalamic and brain thyrotropin-releasing hormone content in the rat and dwarf mouse. Endocrinology 103:1662–1667

    Google Scholar 

  • Roux M, Bartke A, Dumont F, Dubois MP (1982) Immunohistological study of the anterior pituitary gland-pars distalis and pars intermedia-in dwarf mice. Cell Tissue Res 223:415–420

    Google Scholar 

  • Sinha YN, Salocks CB, Vanderlaan WP (1975) Pituitary and serum concentrations of prolactin and GH in Snell dwarf mice. Proc Soc Exp Biol Med 150:207–210

    Google Scholar 

  • Slabaugh MB, Lieberman ME, Rutledge JJ, Gorski J (1981) Growth hormone and prolactin synthesis in normal and homozygous Snell and Ames dwarf mice. Endocrinology 109:1040–1046

    Google Scholar 

  • Smith PE, MacDowell EC (1930) An hereditary anterior-pituitary deficiency in the mouse. Anat Rec 46:249–257

    Google Scholar 

  • Spindler SR, Mellon SH, Baxter JD (1982) Growth hormone gene transcription is regulated by thyroid and glucocorticoid hormones in cultured rat pituitary tumor cells. J Biol Chem 257:11627

    Google Scholar 

  • Vila-Porcile E, Olivier L (1984) The problem of the folliculo-stellate cells in the pituitary gland. In: Motta PM (ed) Ultrastructure of endocrine cells and tissues. Martinus Nijhoff, Boston, pp 64–76

    Google Scholar 

  • Wallis M, Dew JA (1973) The bioassay of growth hormone in Snell's dwarf mice: effects of thyroxine and prolactin on the dose-response curve. J Endocrinol 56:235–243

    Google Scholar 

  • Wilson DB (1986) Immunocytochemical analysis of somatotrophs and mammotrophs in the pars distalis of postnatal dwarf dw mutant mice. Cell Tissue Res 243:561–565

    Google Scholar 

  • Wilson DB, Wyatt DP (1986a) Ultrastructural immuno-cytochemistry of somatotrophs and mammotrophs in embryos of the dwarf mutant mouse. Anat Rec 215:282–287

    Google Scholar 

  • Wilson DB, Wyatt DP (1986b) Immunocytochemistry of TSH cells during development of the dwarf mutant mouse. Anat Embryol (Berl) 174:277–282

    Google Scholar 

  • Yashiro T, Arai M, Miyashita E, Yamashita K, Suzuki T (1988) Fine-structural and immunohistochemical study of anterior pituitary cells of Snell dwarf mice. Cell Tissue Res 251:249–255

    Google Scholar 

  • Yoshimura F, Soji T, Sato S, Yokoyama M (1977) Development and differentiation of rat pituitary follicular cells under normal and some experimental conditions with special reference to an interpretation of renewal cell system. Endocrinol Jpn 24:435–449

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Wilson, D.B., Wyatt, D.P. Immunocytochemical effects of thyroxine stimulation on the adenohypophysis of dwarf (dw) mutant mice. Cell Tissue Res 274, 579–585 (1993). https://doi.org/10.1007/BF00314556

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00314556

Key words

Navigation