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Lactation-associated redistribution of the glial fibrillary acidic protein within the supraoptic nucleus

An immunocytochemical study

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Summary

Electron-microscopic evidence indicates that during conditions of high hormone demand such as lactation there is a dramatic reduction in the number of fine glial processes which are normally interposed between magnocellular neuroendocrine cell somata in the supraoptic nucleus (SON). The purpose of this study was to corroborate these data at the light-microscopic level and to gain some insight into what underlying events might accompany these apparent morphological changes. The distribution of the glial fibrillary acidic protein (GFAP), an intermediate filament component of the astrocytic cytoskeleton, was visualized in lactating or estrous rats using peroxidase-antiperoxidae immunocytochemistry. Computerized image analysis was employed to determine and compare the staining distributions of this protein for the two groups of rats. Statistical analysis revealed a redistribution of GFAP immunostaining in the SONs of lactating animals as compared to controls. No differences in staining were found in a control area dorsolateral to SON. The pattern of change was to a less dense, more homogeneous distribution of GFAP in lactating rats, a change which could be interpreted as reflective of a reduction in the number of densely staining glial processes.

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References

  • Benno RH, Tucker LW, Joh TH, Reis DJ (1982) Quantitative immunocytochemistry of tyrosine hydroxylase in rat brain I. Development of a computer assisted method using the peroxidase-antiperoxidase technique. Brain Res 246:225–236

    Google Scholar 

  • Ciesielski-Treska J, Guerold B, Aunis D (1982a) Immunofluorescence study on the organization of actin in astroglial cells in primary cultures. Neuroscience 7:509–522

    Google Scholar 

  • Ciesielski-Treska J, Bader M-F, Aunis D (1982b) Microtubular organization in flat epitheloid and stellate process bearing astrocytes in culture. Neurochem Res 7:275–285

    Google Scholar 

  • Cowen T, Burnstock G (1982) Image analysis of catecholamine fluorescence. Brain Res Bull 9:81–86

    Google Scholar 

  • Dahl D (1981) The vimentin-GFA protein transition occurs at the time of myelination. J Neurosci Methods 6:741–748

    Google Scholar 

  • Dahl D, Bignami A (1975) Glial fibrillary acidic protein from normal and gliosed human brain. Demonstration of multiple related polypeptides. Biochim Biophys Acta 386:41–51

    Google Scholar 

  • Dahl D, Bignami A (1977) Effect of sodium dodecyl sulfate on the immunogenic properties of the glial fibrillary acidic protein. J Immunol Methods 17:201–209

    Google Scholar 

  • Dahl D, Bignami A, Weber K, Osborn M (1981a) Filament proteins in rat optic nerves undergoing Wallerian degeneration: localization of vimentin, the fibroblastic 100-A filament protein, in normal and reactive astrocytes. Exp Neurol 73:496–506

    Google Scholar 

  • Dahl D, Reuger DC, Bignami A (1981b) Vimentin, the 57,000 molecular weight protein of fibroblast filaments is the major cytoskeletal component in immature glia. Eur J Cell Biol 24:191–196

    Google Scholar 

  • Duffy PE (1982) Glial fibrillary acidic protein and induced differentiation of glia in vitro. J Neurological Sciences, 53:443–460

    Google Scholar 

  • Duffy PE (1983) Astrocytes: normal, reactive, and neoplastic. Raven Press, New York

    Google Scholar 

  • Duffy PE, Rapport MM, Graf L (1980) Glial fibrillary acidic protein and Alzheimer-type senile dementia. Neurology 30:778–782

    Google Scholar 

  • Duffy PE, Huang Y-Y, Rapport MM (1982) The relationship of glial fibrillary acidic protein to the shape, motility, and differentiation of human astrocytoma cells. Exp Cell Res 139:145–157

    Google Scholar 

  • Eng LF, DeArmond SJ (1981) Glial fibrillary acidic (GFA) protein immunocytochemistry in development and neuropathology. In: Acosta Vidrio E, Federoff S (eds) Progress in clinical and biological research, vol 59A, Glial and neuronal cell biology. Alan R Liss, Inc New York

    Google Scholar 

  • Fedoroff S, White R, Subrahmanyan L, Kalnins VI (1981) Properties of putative astrocytes in colony cultures of mouse neopallium. In: Acosta Vidrio E, Federoff S (eds) Progress in clinical and biological research, vol 59A, Glial and neuronal cell biology. Alan R Liss, Inc New York, pp 1–19

    Google Scholar 

  • Gill JL (1978) Design and analysis of experiments. Vol 2. The Iowa State University Press, Ames

    Google Scholar 

  • Glass GV, Stanley JC (1970) Statistical methods in education and psychology, Prentice-Hall, Inc, Englewood Cliffs

    Google Scholar 

  • Gregory WA, Tweedle CD, Hatton GI (1980) Ultrastructure of neurons in the paraventricular nucleus of normal, dehydrated, and rehydrated rats. Brain Res Bull 5:301–306

    Google Scholar 

  • Hatton GI (1976) Nucleus circularis: Is it an osmoreceptor in the brain? Brain Res Bull 1:123–131

    Google Scholar 

  • Hatton GI, Tweedle CD (1982) Magnocellular neuropeptidergic neurons in hypothalamus: increases in membrane apposition and number of specialized synapses from pregnancy to lactation. Brain Res Bull 8:197–204

    Google Scholar 

  • Hatton GI, Walters JK (1973) Induced multiple nucleoli, nucleolar margination, and cell size changes in supraoptic neurons during dehydration and rehydration in the rat. Brain Res 59:137–157

    Google Scholar 

  • Hatton GI, Hutton UE, Hoblitzell ER, Armstrong WE (1976) Morphological evidence for two populations of magnocellular elements in the rat paraventricular nucleus. Brain Res 108:187–193

    Google Scholar 

  • Itoh K, Konishi A, Nomura S, Mizuno N, Nakamura Y, Sugimoto T (1979) Application of a coupled oxidation reaction to electron microscopic demonstration of horseradish peroxidase: cobaltglucose oxidase method. Brain Res 175:341–346

    Google Scholar 

  • Khachaturian H, Sladek JR Jr (1980) Simultaneous monoamine histofluorescence and neuropeptide immunocytochemistry: III. Ontogeny of catecholamine varicosities and neurophysin neurons in the rat supraoptic and paraventricular nuclei. Peptides 1:77–95

    Google Scholar 

  • Latov N, Nilaver G, Zimmerman EA, Johnson WG, Silverman A-J, Defendini R, Cote L (1979) Fibrillary astrocytes proliferate in response to brain injury. Dev Biol 72:381–384

    Google Scholar 

  • Narumi S, Kimelberg HK, Bourke RS (1978) Effects of norepinephrine on the morphology and some enzyme activities of primary monolayer cultures from rat brain. J Neurochem 31:1479–1490

    Google Scholar 

  • Perlmutter LS, Tweedle CD, Hatton GI (1984) Neuronal-glial plasticity in the supraoptic dendritic zone: dendritic bundling and double synapse formation at parturition. Neuroscience 13:769–779

    Google Scholar 

  • Peters A, Palay SL, Webster H (1976) The fine structure of the nervous system: The neurons and supporting cells. WB Saunders Company, Philadelphia, p 246, frontispiece

    Google Scholar 

  • Rueger DC, Huston JS, Bignami A (1979) Formation of 100 Å filaments from purified glial fibrillary acidic protein in vitro. J Mol Biol 135:53–68

    Google Scholar 

  • Salm AK, Hatton GI (1980) An immunocytochemical study of astrocytes associated with the rat supraoptic nucleus. Soc Neurosci Absts 6:547

    Google Scholar 

  • Schachner M, Hedley-Whyte ET, Hsu DW, Schoonmaker G, Bignami A (1977) Ultrastructural localization of glial fibrillary acidic protein in mouse cerebellum by immunoperoxidase labelling. J Cell Biol 75:67–73

    Google Scholar 

  • Schechter R, Yen S-H C, Terry RD (1981) Fibrous astrocytes in senile dementia of the Alzheimer type. J Neuropathol Exp Neurol 40:95–101

    Google Scholar 

  • Schlaepfer WW, Zimmerman U-J P (1981) Calcium-mediated breakdown of glial filaments and neurofilaments in rat optic nerve and spinal cord. Neurochem Res 6:243–255

    Google Scholar 

  • Smithson KG, MacVicar BA, Hatton GI (1983) Polyethylene glycol embedding: A technique compatible with immunocytochemistry, enzyme histochemistry, histofluorescence and intracellular staining. J Neurosci Methods 7:27–41

    Google Scholar 

  • Sternberger LA (1974) Immunocytochemistry. Foundations of immunology series. Prentice Hall, Inc New Jersey, pp 129–171

    Google Scholar 

  • Swaab DF, Pool CW, Nijveldt F (1975) Immunofluorescence of vasopressin and oxytocin in the rat hypothalamo-neurohypophyseal system. J Neural Trans 36:195–215

    Google Scholar 

  • Theodosis DT, Poulain DA (1984) Evidence for structural plasticity in the supraoptic nucleus of the rat hypothalamus in relation to gestation and lactation. Neuroscience (in press)

  • Theodosis DT, Poulain DA, Vincent J-D (1981) Possible morphological basis for synchronisation of neuronal firing in the rat supraoptic nucleus during lactation. Neuroscience 6:919–929

    Google Scholar 

  • Trimmer P, Reier P, Oh T (1980) Morphological studies of normal and induced astrocytic differentiation in vitro. Soc Neurosci Absts 6:291

    Google Scholar 

  • Tweedle CD, Hatton GI (1976) Ultrastructure comparisons of neurons of supraoptic and circularis nuclei in normal and dehydrated rats. Brain Res Bull 1:103–121

    Google Scholar 

  • Tweedle CD, Hatton GI (1977) Ultrastructural changes in rat hypothalamic neurosecretory cells and their associated glia during minimal dehydration and rehydration. Cell Tissue Res 181:59–72

    Google Scholar 

  • Tweedle CD, Hatton GI (1980) Evidence for dynamic interactions between pituicytes and neurosecretory axons in the rat. Neuroscience 5:661–667

    Google Scholar 

  • Tweedle CD, Hatton GI (1982) Magnocellular neuropeptidergic terminals in neurohypophysis: Rapid glial release of enclosed axons during parturition. Brain Res Bull 8:205–209

    Google Scholar 

  • Tweedle CD, Hatton GI (1984) Ultrastructure of catecholaminergic synapses in the rat supraoptic nucleus. Soc Neurosci Absts 10:209

    Google Scholar 

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This work was supported by NIH grant NS09140. We thank Dr. R. Dubes for the use of the Pattern Recognition and Image Analysis Laboratory, Michigan State University, and Dr. W.M. Bukowski for execution of the BMDP statistical program. Special thanks to Drs. G. Nilaver and E.A. Zimmerman for the gift of the anti-GFAP and preimmune sera. Also, thanks go to K.M. Grant for excellent technical assistance. The comments on an earlier draft of the manuscript by Drs. P. Cobbett, A.A. Nunez, R.P. Skoff, and C.D. Tweedle are greatly appreciated.

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Salm, A.K., Smithson, K.G. & Hatton, G.I. Lactation-associated redistribution of the glial fibrillary acidic protein within the supraoptic nucleus. Cell Tissue Res. 242, 9–15 (1985). https://doi.org/10.1007/BF00225557

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