Skip to main content
Log in

Electron-microscopic cytochemistry of alkaline-phosphatase activity in endothelium, pericytes and oligodendrocytes in the rat brain

  • Published:
Histochemistry Aims and scope Submit manuscript

Summary

The fine structural localization of alkaline-phosphatase (ALP) activity was investigated in the endothelial cells and pericytes of blood vessels and in the oligodendrocytes of rat cerebral cortex and corpus callosum by means of electron-microscopic (EM) cytochemistry using the leadcitrate method. ALP activity was associated with both the luminal and abluminal plasma membranes of some endothelial cells, but in other endothelial cells, this activity was found inside the cytoplasm. In some pericytes, ALP activity was associated with the plasma membrane but in others, strong activity was exhibited within both the cytoplasm and nucleus. Light, medium and dark oligodendrocytes showed ALP activity on their plasma membranes; on the other hand, immature oligodendrocytes exhibited activity within the cytoplasma and on the part of their plasma membrane. Within the cytoplasm of these reacted immature cells, the rough endoplasmic reticulum, nuclear membrane and outer membrane of the mitochondria were the main sites of ALP reaction. Endothelial cells, pericytes and oligodendrocytes demonstrated ALP activity along their plasma membrane or within their cytoplasm, and pericytes showed it within their nuclei. In particular, oligodendrocytes retained ALP activity throughout their cell life, and the intracellular distribution of this activity altered as they matured.

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

  • Benham F, Cottell DC, Franks LM, Wilson PD (1977) Alkaline phosphatase activity in human bladder tumor cell lines. J Histochem Cytochem 25:266–274

    Google Scholar 

  • Brightinan MW, Reese TS (1969) Junctions between intimately apposed cell membranes in the vertebrate brain. J Cell Biol 40:648–677

    Google Scholar 

  • Brightman MW, Klatzo L, Olsson Y, Reese TS (1970) The blood-brain barrier to proteins under normal and pathological conditions. J Neurol Sci 10:215–239

    Google Scholar 

  • Ciani F, Contestabile A, Minelli G, Quaglia A (1973) Ultrastructural localization of alkaline phosphatase in cultures of nervous tissue in vitro. J Neurocytol 2:105–116

    Google Scholar 

  • Clark SL (1961) The localization of alkaline phosphatase in tissues of mice, using the electron microscope. Am J Anat 109:57–83

    Google Scholar 

  • Friede RL (1966) A quantitative mapping of alkaline phosphatase in the brain of the rhesus monkey. J Neurochem 13:197–203

    Google Scholar 

  • Hugon J, Borgers M (1968) Fine structural localization of acid and alkaline phosphatase activities in the absorbing cells of the duodenum of rodents. Histochemie 12:42–66

    Google Scholar 

  • Iijima K, Shantha TR, Bourne GH (1967) Enzyme-histochemical studies on the hypothalamus with special reference to the supraoptic and paraventicular nuclei of squirrel monkey. Z Zellforsch 79:76–91

    Google Scholar 

  • Izquierdo L, Marticorena P (1975) Alkaline phosphatase in preimplantation mouse embryos. Exp Cell Res 92:399–402

    Google Scholar 

  • Kaiya H, Moriuchi I, Mikami T, Weikert M, Kreutzberg GW (1976) Increase of alkaline phosphatase in the blood vessel walls as a parameter for axon reaction and its blocking by actinomycin D. Adv Neurol Sci (Tokyo) 20:131–139

    Google Scholar 

  • Karasaki S (1975) Cell proliferation and subcellular localization of alkaline phosphatase activity in rat liver parenchyma during azo dye carcinogenesis. Cancer Res 35:482–491

    Google Scholar 

  • Landow H, Kabat EA, Newman W (1942) Distribution of alkaline phosphatase in normal and in neoplastic tissues of the nervous system. A histochemical study. Arch Neurol Psychiat 48:518–530

    Google Scholar 

  • Leduc EH, Wislocki GB (1952) The histochemical localization of acid and alkaline phosphatases, non-specific esterase and succinic dehydrogenase in the structures comprising the hematoencephalic barrier of the rat. J Comp Neurol 97:242–279

    Google Scholar 

  • Lewinson D, Toister Z, Silbermann M (1982) Quantitative and distributional changes in the activity of alkaline phosphatase during the maturation of cartilage. J Histochem Cytochem 30:261–269

    Google Scholar 

  • Lin C, Sasaki M, Orcutt ML, Miyayama H, Singer RM (1976) Plasma membrane localization of alkaline phosphatase in HeLa cells. J Histochem Cytochem 24:659–667

    Google Scholar 

  • Maekawa H, Yamana K (1975) Alkaline phosphatase isozymes of xenopus laevis embryos and tissues. J Exp Zool 192:155–164

    Google Scholar 

  • Makita T, Sandborn EB (1970) The ultrastructural localization of adenosinetriphosphatase and alkaline phosphatase activity in eosinophyl leukocytes. Histochemie 24:99–105

    Google Scholar 

  • Matsuura H, Hirose I, Fujita K (1970) Electron microscopic localization of alkaline phosphatase in the trigeminal ganglion of the rat. Histochemie 23:91–97

    Google Scholar 

  • Mayahara H, Hirano H, Saito T, Ogawa K (1967) The new lead citrate method for the ultracytochemical demonstration of activity of non-specific alkaline phosphatase (Orthophosphoric monoester phosphohydrolase). Histochemie 11:88–96

    Google Scholar 

  • Melnykovych G, Bishop CF, Swayze MA (1967) Fluctuation of alkaline phosphatase activity in synchronized heteroploid cell cultures: Effects of prednisolone. J Cell Physiol 70:231–236

    Google Scholar 

  • Mizutani A, Barrnett RJ (1965) Fine structural demonstration of phosphatase activity at pH 9. Nature 206:1001–1003

    Google Scholar 

  • Mölbert RG, Duspiva F, von Deimling OH (1960) The demonstration of alkaline phosphatase in the electron microscope. J Biophys Biochem Cytol 7:387–390

    Google Scholar 

  • Mori, S, Leblond CP (1969a) Identification of microglia in light and electron microscopy. J Comp Neurol 135:57–80

    Google Scholar 

  • Mori S, Leblond CP (1969b) Electron microscopic features and proliferation of astrocytes in the corpus callosum of the rat. J Comp Neurol 137:197–226

    Google Scholar 

  • Mori S, Leblond CP (1970) Electron microscopic identification of three classes of oligodendrocytes and a preliminary study of their proliferative activity in the corpus callosum of young rats. J Comp Neurol 139:1–30

    Google Scholar 

  • Nardy K, Bourne GH (1963) Histochemistry of alkaline phosphatase in brain and spinal cord. Nature 200:1216–1217

    Google Scholar 

  • Ovtscharoff W (1973) Ultracytochemische Lokalisierung der alkalischen phosphatase in Cortex cerebri bei neugeborenen Ratten. Histochemie 37:93–95

    Google Scholar 

  • Peters A, Palay SL, Webster MDeF (1976) The fine structure of the nervous system: The neurons and supporting cells. Saunders, Philadelphia

    Google Scholar 

  • Reale E (1962) Electron microscopic localization of alkaline phosphatase from material prepared with the cryostatmicrotome. Exp Cell Res 26:210–211

    Google Scholar 

  • Reese TS, Karnovsky MJ (1967) Fine structural localization of a blood-brain barrier to exogenous peroxidase. J Cell Biol 34:207–217

    Google Scholar 

  • Roots BI (1981) Comparative studies on glial markers. J Exp Biol 95:167–180

    Google Scholar 

  • Rubini JR, Keller S, McCall MS (1964) Inhibition of tritiated thymidine incorporation into DNA by alkaline phosphatase preparation. Cancer Res 24:655–661

    Google Scholar 

  • Sasaki M, Fishman WH (1973) Ultrastructural studies on Regan and non-Regan isozymes of alkaline phosphatase in human ovarian cancer cells. Cancer Res 33:3008

    Google Scholar 

  • Shimizu N (1950) Histochemical studies on the phosphatase of the nervous system. J Comp Neurol 93:201–217

    Google Scholar 

  • Skoff RP, Price DL, Stocks A (1976) Electron microscopic autoradiographic studies of gliogenesis in rat optic nerve. I. Cell proliferation. J Comp Neurol 169:291–312

    Google Scholar 

  • Sugimura K, Mizutani A (1979) Histochemical and cytochemical studies of alkaline phosphatase activity in the synapses of rat brain. Histochemistry 61:123–129

    Google Scholar 

  • Tewari HB, Bourne GH (1964) Histochemical studies on the distribution of alkaline and acid phosphatases and 5-nucleotidase in the trigeminal ganglion cells of rat. Acta Histochem 17:197–207

    Google Scholar 

  • Tokumitsu S, Fishman WH (1983) Alkaline phosphatase biosynthesis in the endoplasmic reticulum and its transport through the Golgi apparatus to the plasma membrane: Cytochemical evidence. J Histochem Cytochem 31:647–655

    Google Scholar 

  • Varon S (1978) Macromolecular glial cell markers. In: Schoffeiniels E (ed) Dynamic properties of glial cells. Pergamon Press, Oxford, pp 93–103

    Google Scholar 

  • Varon S, Somjen GG (1979) Neuron-glia interactions. III. Chemical markers and neuroglia. Neurosci Res Program Bull 17:42–65

    Google Scholar 

  • Westergaard E, Brightman MW (1973) Transport of proteins across normal cerebral arterioles. J Comp Neurol 152:17–44

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Mori, S., Nagano, M. Electron-microscopic cytochemistry of alkaline-phosphatase activity in endothelium, pericytes and oligodendrocytes in the rat brain. Histochemistry 82, 225–231 (1985). https://doi.org/10.1007/BF00501399

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00501399

Keywords

Navigation