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Immunocytochemical mapping of basic fibroblast growth factor in the developing and adult rat adrenal gland

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Summary

We studied the spatial and temporal pattern of basic fibroblast growth factor (bFGF) immunoreactivity in the rat adrenal gland during postnatal development. In the cortex the glomerulosa zone reveals a strong anti-bFGF immunoreactivity at all developmental ages studied. In the fasciculata zone the high number of anti-bFGF immunoreactive cells in the first week decreases during the second and third week. The late developing reticularis zone shows only few anti-bFGF labeled cells at all postnatal ages. This distributional pattern of bFGF immunoreactivity matches that of mitotic activity in the rat adrenal cortex strengthening the role of bFGF as an autocrine growth factor for adrenocortical cells. In the medulla anti-bFGF positive chromaffin cells become detectable at postnatal day (P) 8 and increase in number during the second and third week. In the adult rat the staining intensity of the chromaffin cells was higher than at P18. In the adult medulla bFGF colocalizes with noradrenaline suggesting its presence in a chromaffin cell subpopulation. In accordance with previous results the role of the chromaffin cell bFGF as a neurotrophic factor for preganglionic sympathetic neurons is discussed.

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References

  • Anderson KJ, Dan D, Lee A, Cotman CW (1988) Basic fibroblast growth factor prevents death of lesioned cholinergic neurons in vivo. Nature 332:360–361

    Article  PubMed  CAS  Google Scholar 

  • Baird A, Böhlen P (1990) Fibroblast growth factors. In: Sporn MB, Roberts AB (eds) Handbook of experimental pharmacology. Peptide growth factors and their receptors. Springer, Berlin Heidelberg, New York (in press)

    Google Scholar 

  • Baxter JS (1946) The growth cycle of the cells of the adrenal cortex in the adult rat. J Anat 80:139–146

    PubMed  CAS  Google Scholar 

  • Blottner D, Unsicker K (1989) Spatial and temporal patterns of neurotrophic activities in rat adrenal medulla and cortex. Dev Brain Res 48:243–253

    Article  CAS  Google Scholar 

  • Blottner D, Westermann R, Grothe C, Böhlen P, Unsicker K (1989) Basic fibroblast growth factor in the adrenal gland: possible trophic role for preganglionic neurons in vivo. Eur J Neurosci 1:471–478

    Article  PubMed  Google Scholar 

  • Böhlen P (1989) Fibroblast growth factor. In: Sorg C (ed) Macrophage-derived cell regulatory factors, vol 1. Karger Basel, pp 204–228

    Google Scholar 

  • Davies AM, Bantlow C, Heuman R, Korsching S, Rohrer H, Thoenen H (1987) The timing and site of nerve growth factor (NGF) synthesis in developing skin in relation to its innervation by sensory neurons and their expression of NGF receptors. Nature 326:353–358

    Article  PubMed  CAS  Google Scholar 

  • Gospodarowicz D, Neufeld G, Schweigerer L (1986a) Molecular and biological characterization of fibroblast growth factor, an angiogenic factor which controls the proliferation and differentiation of measoderm and neuroectodermal derived cells. Cell Differ 19:1–17

    Article  PubMed  CAS  Google Scholar 

  • Gospodarowicz D, Baird A, Cheng J, Lui GM, Esch F, Böhlen P (1986b) Isolation of fibroblast growth factor from bovine adrenal gland: physicochemical and biological characterization. Endocrinology 118:82–90

    PubMed  CAS  Google Scholar 

  • Gospodarowicz D, Neufeld G, Schweigerer L (1986c) Fibroblast growth factor. Mol Cell Endocrinol 46:187–204

    Article  PubMed  Google Scholar 

  • Grothe C, Hofmann H-D, Verhofstad AAJ, Unsicker K (1985) Nerve growth factor and dexamethasone specify the catecholaminergic phenotype of cultured rat chromaffin cells: dependence on developmental stage. Dev Brain Res 21:125–132

    Article  CAS  Google Scholar 

  • Grothe C, Otto D, Unsicker K (1989) Basic fibroblast growth factor promotes in vitro survival and cholinergic development of rat septal neurons: comparison with the effects of nerve growth factor. Neuroscience 31:649–661

    Article  PubMed  CAS  Google Scholar 

  • Grothe C, Zachmann K, Unsicker K, Westermann R (1990) High molecular weight forms of basic fibroblast growth factor recognized by a new anti-bFGF antibody. FEBS Lett 260:35–38

    Article  PubMed  CAS  Google Scholar 

  • Grothe C, Unsicker K (1989) Immunocytochemical localization of basic fibroblast growth factor in bovine adrenal gland, ovary, and pituitary. J Histochem Cytochem 37:1877–1883

    PubMed  CAS  Google Scholar 

  • Grynszpan-Winograd O (1974) Adrenaline and noradrenaline cells in the adrenal medulla of the hamster: a morphological study of their innervation. J Neurocytol 3:341–361

    Article  PubMed  CAS  Google Scholar 

  • Günther G (1972) Mitosen Zellvermehrung und Zellverschiebung in der Nebenniere. Endokrinologie 60: 356–378

    PubMed  Google Scholar 

  • Hirano T (1981) Characteristics and functions of two types of efferent fibers in the adrenal nerve. J Auton Nerv Syst 4:339–350

    Article  PubMed  CAS  Google Scholar 

  • Jurecka W, Lassmann H, Hörander H (1978) The proliferation of adrenal medullary cells in newborn and adult mice. Cell Tissue Res 189:305–312

    Article  PubMed  CAS  Google Scholar 

  • Kahri A (1966) Histochemical and electron microscopic studies on cells of the rat adrenal cortex in tissue culture. Acta Endocrinol [Suppl] Copenhagen 52: 108

    Google Scholar 

  • Kirby RF, McCarty R (1987) Ontogeny of functional sympathetic innervation to the heart and adrenal medulla in the preweanling rat. J Auton Nerv Syst 19:67–75

    Article  PubMed  CAS  Google Scholar 

  • Kondo H, Kuramoto H, Fujita T (1986) An immuno-electronmicroscopic study of the localization of VIP-like immunoreactivity in the adrenal gland of the rat. Cell Tissue Res 245:531–538

    Article  PubMed  CAS  Google Scholar 

  • Kuramoto H, Kondo H, Fujita T (1987) Calcitonin gene-related peptide (CGRP)-like immunoreactivity in scattered chromaffin cells and nerve fibers in the adrenal gland of rats. Cell Tissue Res 247:309–315

    Article  PubMed  CAS  Google Scholar 

  • Lewis PR, Shute CCD (1969) An electron microscopic study of cholinesterase distribution in the rat adreanal medulla. J Microsc 89:181–193

    PubMed  CAS  Google Scholar 

  • Lobb RR (1988) Clinical applications of heparin-binding growth factor. Eur J Clin Invest 18:321–336

    Article  PubMed  CAS  Google Scholar 

  • Long JA (1975) Zonation of the mammalian adrenal cortex. In: Geiger SR (ed) Handbook of physiology, sect 7, vol VI. American Physiological Society, Washington DC pp 13–24

    Google Scholar 

  • Lundberg JM, Hökfelt T, Hemsen A, Theodersson-Norheim E, Pernow J, Hamberger B, Goldstein M (1986) Neuropeptide Y-like immunoreactivity in adrenaline cells of adrenal medulla and in tumors and plasma of pheochromocytoma patients. Regul Pept 13:169–182

    Article  PubMed  CAS  Google Scholar 

  • Mikhail Y (1973) Early stages in postnatal development of the adrenal gland. Acta Anat (Basel) 84:138–149

    CAS  Google Scholar 

  • Mitchell RM (1948) Histological changes and mitotic activity in the rat adrenal during postnatal development. Anat Rec 101:161–185

    Article  PubMed  CAS  Google Scholar 

  • Morrison RS, Sharma A, de Vellis J, Bradshaw RA (1986) Basic fibroblast growth factor supports the survival of cerebral cortical neurons in primary culture. Proc Natl Acad Sci USA 83:7537–7541

    Article  PubMed  CAS  Google Scholar 

  • Otto D, Unsicker K, Grothe C (1987) Pharmacological effects of nerve growth factor and fibroblast growth factor applied to the transectioned sciatic nerve on neuron death in adult rat dorsal root ganglia. Neurosci Lett 83:156–160

    Article  PubMed  CAS  Google Scholar 

  • Otto D, Frotscher M, Unsicker K (1989) Basic fibroblast growth factor and nerve growth factor administered in gelfoam rescue medial septal neurons after fimbria formix transection. J Neurosci Res 22:83–91

    Article  PubMed  CAS  Google Scholar 

  • Schweigerer L, Neufeld G, Friedman J, Abraham JA, Fiddes JC, Gospodarowicz D (1987) Basic fibroblast growth factor: production and growth stimulation in cultured adrenal cortex cells. Endocinology 120:796–800

    Article  CAS  Google Scholar 

  • Sievers J, Hausmann B, Unsicker K, Berry M (1987) Fibroblast growth factors promote survival of adult retinal ganglion cells after transection of the optic nerve. Neurosci Lett 76:157–162

    Article  PubMed  CAS  Google Scholar 

  • Tischler AS, Ruzicka LA, Donahue SR, DeLellis RA (1989) Chromaffin cell proliferation in the adult rat adrenal medulla. Int J Dev Neurosci 7:439–448

    Article  PubMed  CAS  Google Scholar 

  • Unsicker K, Reichert-Preibsch H, Schmidt R, Pettmann B, Labourdette G, Sensenbrenner M (1987) Astroglial and fibroblast growth factors have neurotrophic functions for cultured peripheral and central nervous system neurons. Proc Natl Acad Sci USA 84:5459–5463

    Article  PubMed  CAS  Google Scholar 

  • Unsicker K, Blottner D, Gehrke D, Grothe C, Heymann D, Stögbauer F, Westermann R (1988a) Neuroectodermal cells: storage and release of growth factors. In: Gorio A, Perez-Polo J, deVellis J, Haber B (eds) NATO ASI Series, vol. H22. Springer, Berlin Heidelberg New York, pp 43–55

    Google Scholar 

  • Unsicker K, Westermann R, Grothe C, Gehrke D, Böhlen P (1988b) A possible autocrine role of basic FGF for mainternance and transmitter storage of chromaffin cells. Soc Neurosci Abstr 14:301

    Google Scholar 

  • Walicke P, Cowman WM, Ueno N, Baird A, Guillemin R (1986) Fibroblast growth factor promotes survival of dissociated hippocampal neurons and enhances neurite extension. Proc Natl Acad Sci USA 83:3012–3016

    Article  PubMed  CAS  Google Scholar 

  • Westermann R, Johannsen M, Unsicker K, Grothe C (1990) Basic fibroblast growth factor (bFGF) immunoreactivity is present in chromaffin granules. J Neurosci (in press)

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Grothe, C., Unsicker, K. Immunocytochemical mapping of basic fibroblast growth factor in the developing and adult rat adrenal gland. Histochemistry 94, 141–147 (1990). https://doi.org/10.1007/BF02440180

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