Skip to main content
Log in

Transcytosis of protein through the mammalian cerebral epithelium and endothelium. I. Choroid plexus and the blood-cerebrospinal fluid barrier

  • Published:
Journal of Neurocytology

    We’re sorry, something doesn't seem to be working properly.

    Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Summary

The potential for transcytosis (endocytosis → intracellular transport → exocytosis) of protein and membrane events associated with fluid phase and adsorptive endocytic processes within epithelia of the choroid plexus [blood-cerebrospinal fluid (CSF) barrier] were investigated in mice injected intravenously or into the lateral cerebral ventricle with native horseradish peroxidase (HRP) or the lectin wheatgerm agglutinin (WGA) conjugated to HRP. WGA binds to specific cell surface oligosaccharides and enters cells by the process of adsorptive endocytosis; native HRP is taken into cells non-specifically by fluid phase endocytosis. The lysosomal system of organelles and the endoplasmic reticulum, identified by enzyme cytochemical markers applied to choroid epithelia, were analysed for possible participation in transcytosis and compared to epithelial organelles harbouring the exogenous tracer proteins. Blood-borne native HRP was endocytosed readily by choroid epithelia whereas WGA-HRP was not, perhaps because WGA-HRP does not escape fenestrated endothelia as easily as native HRP. The blood-borne proteins incorporated within endocytic vesicles by choroid epithelia were directed to endosomes (prelysosomes) and secondary lysosomes (e.g. tubules, multivesicular/dense bodies) for eventual degradation and did not reach the apical/microvillus surface. Both CSF-borne native HRP and WGA-HRP entered choroid epithelia within endocytic vesicles derived from the microvillus border. Native HRP, ultimately sequestered within endosomes and secondary lysosomes, failed to undergo transcytosis through the epithelia into the basolateral clefts. Conversely, CSF-borne WGA-HRP was transported through the epithelia and released into the basolateral clefts within 10 min post-injection. The lectin conjugate labelled epithelial vesicles, endosomes, secondary lysosomes and, at 30 min post-injection, the transmost saccule of the Golgi complex which exhibits acid hydrolase activity. Tubular profiles, related either to the endosome apparatus or to the lysosomal system, and the endoplasmic reticulum did not appear involved in the transcytotic pathway. The data suggest that CSF-borne protein entering the choroid epithelium by adsorptive endocytosis can undergo rapid transcytosis through the cell. The results provide insight to transcytotic pathways utilizing vesicles, the endosomal apparatus, and the Golgi complex within the choroid epithelium for circumventing the blood-CSF barrier. Hypothesized membrane events and morphological associations among constituents of the endomembrane system within the choroid epithelium are summarized diagrammatically.

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

  • Balin, B. J. &Broadwell, R. D. (1987) Lectin-labeled membrane is transferred to the Golgi complex in mouse pituitary cellsin vivo, Journal of Histochemistry and Cytochemistry 35 489–98.

    Google Scholar 

  • Balin, B. J., Broadwell, R. D. &Salcman, M. (1987) Tubular profiles do not form transendothelial channels through the blood-brain barrier.Journal of Neurocytology 16, 721–35.

    Google Scholar 

  • Balin, B. J., Broadwell, R. D., Salcman, M. &Elkalliny, M. (1986) Avenues for entry of peripherally administered protein to the CNS in mouse, rat and monkey.Journal of Comparative Neurology 251, 260–80.

    Google Scholar 

  • Becker, N. H. &Almazon, R. (1968) Evidence for the functional polarization of micropinocytotic vesicles in the rat choroid plexus,Journal of Histochemistry and Cytochemistry 16, 278–80.

    Google Scholar 

  • Becker, N. H., Novikoff, A. B. &Zimmerman, H. M. (1967) Fine structure observations of the uptake of intravenously injected peroxidase by the rat choroid plexus.Journal of Histochemistry and Cytochemistry 15, 160–5.

    Google Scholar 

  • Bennett, G., Kan, F. W. K. &O'shaughnessy, D. (1981) The site of incorporation of sialic acid residues into giycoproteins and the subsequent fate of these-molecules in various rat and mouse cell types as shown by radioautography after injection of (3H)N-acetylmannosamine. II. Observations in tissues other than liver.Journal of Cell Biology 88, 16–31.

    Google Scholar 

  • Bennett, G. &O'shaughnessy, D. (1981) The site of incorporation of sialic acid residues into glycoproteins and the subsequent fates of these molecules in various rat and mouse cell types as shown by radioautography after injection of (3H)N-acetylmannosamine. I. Observations in hepatocytes.Journal of Cell Biology 88, 1–15.

    Google Scholar 

  • Bergeron, J. J., Cruz, J., Khan, M. N. &Posner, B. I. (1985) Uptake of insulin and other ligands into receptorrich endocytic components of target cells: the endosomal apparatus.Annual Review of Physiology 47, 383–404.

    Google Scholar 

  • Bouchaud, C. &Bouvier, D. (1978) Fine structure of tight junctions between rat choroidal cells after osmotic opening induced by urea and sucrose.Tissue and Cell 10, 331–42.

    Google Scholar 

  • Brightman, M. W. (1968) The intracerebral movement of proteins injected into blood and cerebrospinal fluid of mice.Progress in Brain Research 29, 19–37.

    Google Scholar 

  • Brightman, M. W. (1975) Ultrastructural characteristics of adult choroid plexus: Relation to the blood-cerebrospinal fluid barrier to proteins. InThe Choroid Plexus in Health and Disease (edited byNetsky, M. G. &Shuangshati, S.), pp. 86–112. Charlottesville: University Virginia Press.

    Google Scholar 

  • Brightman, M. W., Klatzo, I., Olsson, Y. &Reese, T. S. (1970) The blood-brain barrier to proteins under normal and pathological conditions.Journal of the Neurological Sciences 10 215–39.

    Google Scholar 

  • Brightman, M. W. &Reese, T. S. (1969) Junctions between intimately opposed cell membrane in the vertebrate brain.Journal of Cell Biology 40, 648–77.

    Google Scholar 

  • Broadwell, R. D. (1988) Movement of macromolecules across the blood-brain barrier. InThe 16th Princeton Conference on Cerebrovascular Diseases (edited byGinsburg, M.). New York: Raven Press (in press).

    Google Scholar 

  • Broadwell, R. D. &Balin, B. J. (1985) Endocytic and exocytic pathways of the neuronal secretory process and trans-synaptic transfer of wheatgerm agglutininhorseradish peroxidasein vivo.Journal of Comparative Neurology 242, 632–50.

    Google Scholar 

  • Broadwell, R. D., Balin, B. J. &Cataldo, A. M. (1987a) Fine structure and cytochemistry of the mammalian median eminence. InCircumventricular Organs and Body Fluids (edited byGross, P. M.), pp. 61–85. Boca Raton, Florida: CRC Press.

    Google Scholar 

  • Broadwell, R. D., Balin, B. J. &Salcman, M. (1987b) Polarity of the blood-brain barrier to the endocytosis of protein.Wiss. Z. Karl-Marx-Univ. Leipzig, Math.-Naturwiss. R. 36, 170–4.

    Google Scholar 

  • Broadwell, R. D., Balin, B. J. &Salcman, M. (1988) Transcytotic pathway for blood-borne protein through the blood-brain barrier.Proceedings of the National Academy of Sciences USA 85, 632–6.

    Google Scholar 

  • Broadwell, R. D., Balin, B. J., Salcman, M. &Kaplan, R. S. (1983) Brain-blood barrier? Yes and no.Proceedings of the National Academy of Sciences USA 80, 7352–6.

    Google Scholar 

  • Broadwell, R. D. &Brightman, M. W. (1979) Cytochemistry of undamaged neurons transporting exogenous proteinin vivo.Journal of Comparative Neurology 185, 31–74.

    Google Scholar 

  • Broadwell, R. D. &Brightman, M. W. (1983) Horseradish peroxidase: A tool to study the neuroendocrine cell and other peptide-secreting cells.Methods in Enzymology 103, 187–218.

    Google Scholar 

  • Broadwell, R. D., Brightman, M. W. &Oliver, C. (1980) Neuronal transport of acid hydrolases and peroxidase within the lysosomal system of organelles: Involvement of agranular reticulum-like cisterns.Journal of Comparative Neurology 190, 519–32.

    Google Scholar 

  • Broadwell, R. D. &Cataldo, A. M. (1984) The neuronal endoplasmic reticulum. Its cytochemistry and contribution to the endomembrane system. II. Axons and terminals.Journal of Comparative Neurology 230, 231–48.

    Google Scholar 

  • Broadwell, R. D., Charlton, H. M., Balin, B. J. &Salcman, M. (1987c) Angioarchitecture of the CNS, pituitary gland, and intracerebral grafts revealed with peroxidase cytochemistry.Journal of Comparative Neurology 260, 47–62.

    Google Scholar 

  • Broadwell, R. D. &Oliver, C. (1983) An enzyme cytochemical study of the endocytic pathways in anterior pituitary cells of the mousein vivo.Journal of Histochemistry and Cytochemistry 31, 325–35.

    Google Scholar 

  • Broadwell, R. D. &Salcman, M. (1981) Expanding the definition of the blood-brain barrier to protein.Proceedings of the National Academy of Sciences (USA) 78, 7820–4.

    Google Scholar 

  • Brown, M. S., Anderson, R. G. W., Barr, S. K. &Goldstein, J. L. (1982) Recycling of cell surface receptors: Observations from the LDL receptor system.Cold Spring Harbor Symposium on Quantitative Biology 46, 713–20.

    Google Scholar 

  • Burwen, J., Barker, M. E., Goldman, I. S., Hradek, G. T., Roper, S. E. &Jones, A. L. (1984) Transport of epidermal growth factor by rat liver: Evidence for a non-lysosomal pathway.Journal of Cell Biology 99, 1259–65.

    Google Scholar 

  • Cataldo, A. M. &Broadwell, R. D. (1986a) Cytochemical identification of cerebral glycogen and glucose-6-phosphatase activity under normal and experimental conditions. I. Neurons and glia.Journal of Electron Microscopy Technique 3, 413–37.

    Google Scholar 

  • Cataldo, A. M. &Broadwell, R. D. (1986b) Cytochemical identification of cerebral glycogen and glucose-6-phosphatase activity under normal and experimental conditions. II. Choroid plexus and ependymal epithelia, endothelia and pericytes.Journal of Neurocytology 15, 511–24.

    Google Scholar 

  • Coomber, B. L. &Stewart, P. A. (1986) Three dimensional reconstruction of vesicles in endothelium of blood-brain barrier versus highly permeable microvessels.Anatomical Record 215, 256–61.

    Google Scholar 

  • Dautry-Varsat, A. &Lodish, H. F. (1983) The Golgi complex and the sorting of membrane and secreted proteins.Trends in Neuroscience 6, 484–90.

    Google Scholar 

  • Dautry-Varsat, A. &Lodish, H. F. (1984) How receptors bring proteins and particles into cells.Scientific American 250, 52–8.

    Google Scholar 

  • Davis, D. A. &Milhorat, T. H. (1975) The blood-brain barrier of the rat choroid plexus.Anatomical Record 181, 779–87.

    Google Scholar 

  • De Bruyn, P. P. H., Michelson, S. &Becker, R. P. (1975) Endocytosis, transfer tubules, and lysosomal activity in myeloid sinusoidal endothelium.Journal of Ultrastructure Research 53, 133–51.

    Google Scholar 

  • Doty, S. B., Smith, C. E., Hand, A. R. &Oliver, C. (1977) Inorganic trimetaphosphatase as a histochemical marker for lysosomes in light and electron microscopy.Journal of Histochemistry and Cytochemistry 25, 1381–4.

    Google Scholar 

  • Dunn, W. A., Connolly, T. P. &Hubbard, A. L. (1986) Receptor-mediated endocytosis of epidermal growth factor by rat hepatocytes: receptor pathway.Journal of Cell Biology 102, 24–36.

    Google Scholar 

  • Dunn, W. A. &Hubbard, A. L. (1984) Receptor-mediated endocytosis of epidermal growth factor by hepatocytes in the perfused rat liver: Ligand and receptor dynamics.Journal of Cell Biology 98, 2148–59.

    Google Scholar 

  • Gomori, G. (1952)Microscopic Histochemistry: Principles and Practice, pp. 189–273. Chicago: University of Chicago Press.

    Google Scholar 

  • Gonatas, J. K. &Avrameas, S. (1973) Detection of plasma membrane carbohydrates with lectin peroxidase conjugates.Journal of Cell Biology 59, 436–45.

    Google Scholar 

  • Gonatas, J. K., Steiber, A., Hickey, W. F., Herbert, S. H. &Gonatas, J. O. (1984) Endosomes and Golgi vesicles in adsorptive and fluid phase endocytosis.Journal of Cell Biology 99, 1379–90.

    Google Scholar 

  • Graham, R. C. &Karnovsky, M. J. (1966) The early stages of absorption of injected horseradish peroxidase in the proximal tubules of mouse kidney: Ultrastructural cytochemistry by a new technique.Journal of Histochemistry and Cytochemistry 14, 291–302.

    Google Scholar 

  • Helenius, A., Mellman, I., Wall, D. &Hubbard, A. (1983) Endosomes.Trends in Biochemical Science 8, 245–9.

    Google Scholar 

  • Mesulam, M.-M. (1978) Tetramethylbenzidine for horseradish peroxidase neurohistochemistry: A non-carcinogenic blue reaction product with superior sensitivity for visualizing neural afferents and efferents.Journal of Histochemistry and Cytochemistry 26, 106–17.

    Google Scholar 

  • Møllgård, K. &Saunders, N. R. (1975) Complex tight junctions of epithelial and endothelial cells in early foetal brain.Journal of Neurocytology 4, 453–68.

    Google Scholar 

  • Møllgård, K. &Saunders, N. R. (1977) A possible transepithelial pathway via endoplasmic reticulum in foetal sheep choroid plexus.Proceedings of the Royal Society of London Series B 199, 321–6.

    Google Scholar 

  • Mueller, S. C. &Hubbard, A. L. (1986) Receptor-mediated endocytosis of asialoglycoproteins by rat hepatocytes: Receptorpositive and receptor-negative endosomes.Journal of Cell Biology 102, 932–42.

    Google Scholar 

  • Novikoff, A. B. (1963) Lysosomes in the physiology and pathology of cells: Contributions of staining methods. InCiba Foundation Symposium on Lysosomes (edited byDeReuck, A. V. S. &Cameron, M. P.), pp. 35–77. Boston: Little, Brown & Co.

    Google Scholar 

  • Oliver, C. (1980) Cytochemical localization of acid phosphatase and trimetaphosphatase activities in exocrine acinar cells,Journal of Histochemistry and Cytochemistry 28, 78–81.

    Google Scholar 

  • Oliver, C. (1983) Characterization of basal lysosomes in exocrine acinar cells.Journal of Histochemistry and Cytochemistry 31, 1209–16.

    Google Scholar 

  • Rodewald, R. (1973) Intestinal transport of antibodies in the newborn rat.Journal of Cell Biology 58, 189–211.

    Google Scholar 

  • Rodewald, R. &Abrahamson, D. R. (1982) Receptormediated transport of IgG through the intestinal epithelium of the neonatal rat.Ciba Foundation Symposium 92, 209–32.

    Google Scholar 

  • Rodewald, R. &Kraehenbuhl, J.-P. (1984) Receptormediated transport of IgG.Journal of Cell Biology 99, 159s-164s.

    Google Scholar 

  • Steinman, R. M., Mellman, I. S., Muller, W. A. &Cohn, Z. A. (1983) Endocytosis and the recycling of plasma membrane.Journal of Cell Biology 96, 1–27.

    Google Scholar 

  • Tangoren, M., Broadwell, R. D., Moriyama, E., Oliver, C. &Wolf, A. (1988) How significant is the blood-brain barrier?Abstracts of the Society for Neuroscience 14, 617.

    Google Scholar 

  • Van Deurs, B. (1976) Choroid plexus absorption of horseradish peroxidase from the cerebral ventricles.Journal of Ultrastructure Research 55, 400–16.

    Google Scholar 

  • Van Deurs, B. (1978) Horseradish peroxidase uptake into the rat choroid plexus epithelium, with special reference to the lysosomal system.Journal of Ultrastructure Research 62, 155–67.

    Google Scholar 

  • Van Deurs, B., Moller, M. &Amtorp, O. (1978) Uptake of horseradish peroxidase from CSF into the choroid plexus of the rat with special reference to transepithelial transport.Cell and Tissue Research 187, 15–23.

    Google Scholar 

  • Van Deurs, B., Von Bulow, F. &Moller, M. (1981) Vesicular transport of cationized ferritin by the epithelium of rat choroid plexus.Journal of Cell Biology 89, 131–9.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Balin, B.J., Broadwell, R.D. Transcytosis of protein through the mammalian cerebral epithelium and endothelium. I. Choroid plexus and the blood-cerebrospinal fluid barrier. J Neurocytol 17, 809–826 (1988). https://doi.org/10.1007/BF01216708

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01216708

Keywords

Navigation