Skip to main content
Log in

A light and electron microscopic study of the intraneuronal transport of horseradish peroxidase and wheat germ agglutinin-peroxidase conjugates in the rat visual system

  • Published:
Journal of Neurocytology

Summary

The ability of horseradish peroxidase (HRP) and the lectin wheat germ agglutinin (WGA) covalently conjugated with HRP to label retrogradely dorsal lateral geniculate nucleus (dLGN) neurons, subsequent to injections of either marker into rat striate cortex, was assessed by counting labelled neurons in the dLGN. Rats injected with either marker in concentrations ranging from 0.1 to 100μg/μl of HRP either free or coupled to WGA were perfused 24 h later and their brains incubated using the chromagen tetramethyl benzidine. At high concentrations (2–100μg/μ1), comparable numbers of labelled neurons were observed in the dLGN but at low concentrations (0.1–1.0μg/μ1), WGA-HRP labelled 2–5 times more dLGN neurons than did unconjugated HRP. The sugarN-acetylglucosamine, and free WGA added in excess to WGA-HRP, abolished the retrograde labelling of dLGN neurons.

In additional rats, which received striate cortex injections of 100μg/μ1 of either free HRP or HRP coupled to WGA, the injection site was studied with electron microscopy after survivals of 30 min to 24 h. Similar organelles in neuronal perikarya, dendrites and axons were labelled by both markers, with the exception that only rats injected with WGA-HRP had labelled GERL in some of their neurons in striate cortex.

It was concluded from these studies that: (1) WGA-HRP is a more sensitive retrograde marker than free HRP at low concentrations in the rat visual system; (2) WGA-HRP binds specifically to moieties with terminalN-acetylglucosamine; and (3) WGA-HRP, but not free HRP, is localized to neuronal GERL of striate cortex subsequent to endocytosis.

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.

Institutional subscriptions

Similar content being viewed by others

References

  • Avrameas, S. &Ternynck, T. (1971) Peroxidase labeled antibody and Fab conjugates with enhanced intracellular penetration.Immunochemistry 8, 1175–9.

    Google Scholar 

  • Brushart, T. M. &Mesulam, M.-M. (1980) Transganglionic demonstration of central sensory projections from skin and muscle with HRP-lectin conjugates.Neurosdence Letters 17, 1–6.

    Google Scholar 

  • Bunt, A. H. &Haschke, R. H. (1978) Features of foreign proteins affecting their retrograde transport in axons of the visual system.journal of Neurocytology 7, 665–78.

    Google Scholar 

  • Bunt, A. H., Haschke, R., Lund, R. D. &Calkins, D. F. (1976) Factors affecting retrograde axonal transport of horseradish peroxidase in the visual system.Brain Research 102, 152–5.

    Google Scholar 

  • Devito, J. L., Clausing, K. W. &Smith, O. A. (1974) Uptake and transport of horseradish peroxidase by cut ends of the vagus nerve.Brain Research 62, 269–71.

    Google Scholar 

  • Dumas, M., Schwab, M. E. &Thoenen, H. (1979) Retrograde axonal transport of specific macromolecules as a tool for characterizing nerve terminal membranes.Journal of Neurobiology 10, 179–97.

    Google Scholar 

  • Farquhar, M. G. (1978) Recovery of surface membrane in anterior pituitary cells. Variations in traffic detected with anionic and cationic ferritin.Journal of Cell Biology 77, R35-R42.

    Google Scholar 

  • Gonatas, N. K. (1979) Immunochemistry and receptors: Studies on the redistribution and adsorptive endocytosis of antiimmunoglobulin antibodies, cholera toxin and lectins. InProgress in Neuropathology Vol. 4. (edited byZimmerman, H. M.), pp. 51–60. New York: Raven Press.

    Google Scholar 

  • Gonatas, N. K. &Avrameas, S. (1973) Detection of plasma membrane carbohydrates with lectin peroxidase conjugates.Journal of Cell Biology 59, 443–63.

    Google Scholar 

  • Gonatas, N. K. &Avrameas, S. (1977) Detection of carbohydrates with lectin peroxidase conjugates. InMethods in Cell Biology Vol. XV (edited byPrescott, D.), pp. 387–406. New York: Academic Press.

    Google Scholar 

  • Gonatas, N. K., Kim, S. U., Stieber, A. &Avrameas, S. (1977) Internalization of lectins in neuronal GERL.Journal of Cell Biology 73, 1–13.

    Google Scholar 

  • Gonatas, N. K., Harper, C., Mizutani, T. &Gonatas, J. O. (1979) Superior sensitivity of conjugates of horseradish peroxidase with wheat germ agglutinin for studies of retrograde axonal transport.Journal of Histochemistry and Cytochemistry 27, 728–34.

    Google Scholar 

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

    Google Scholar 

  • Graybiel, A. M. &Devor, M. (1974) A microelectrophoretic delivery technique for use with horseradish peroxidase.Brain Research 68, 167–73.

    Google Scholar 

  • Gurd, J. W. (1977) Synaptic plasma membrane glycoproteins: Molecular identification of lectin receptors.Biochemistry 16, 369–74.

    Google Scholar 

  • Halperin, J. L. &Lavail, J. H. (1975) A study of the dynamics of retrograde transport and accumulation of horseradish peroxidase in injured neurons.Brain Research 100, 253–69.

    Google Scholar 

  • Hand, A. R. (1980) Cytochemical differentiation of the Golgi apparatus from GERL.Journal of Histochemistry and Cytochemistry 27, 82–6.

    Google Scholar 

  • Harper, C. G., Gonatas, J. O., Stieber, A. &Gonatas, N. K. (1980)In vivo uptake of wheat germ agglutinin-horseradish peroxidase conjugates into neuronal GERL and lysosomes.Brain Research 188, 465–72.

    Google Scholar 

  • Hatten, M. E., Schachner, M. &Sidman, R. L. (1979) Histochemical characterization of lectin binding in mouse cerebellum.Neuroscience 4, 921–35.

    Google Scholar 

  • Hess, H. H., Bass, N. H., Thalheimer, C. &Devarakondra, R. (1976) Gangliosides and the architecture of human frontal and rat somatosensory isocortex.Journal of Neurochemistry 26, 1115–21.

    Google Scholar 

  • Jacobson, S. &Trojanowski, J. Q. (1975) Corticothalamic neurons and thalamocortical terminal fields: An investigation in rat using horseradish peroxidase and autoradiography.Brain Research 85, 385–401.

    Google Scholar 

  • Joseph, K. C., Kim, S. U., Stieber, A. &Gonatas, N. K. (1978) Endocytosis of cholera toxin into neuronal GERL.Proceedings of the National Academy of Science 75, 2815–9.

    Google Scholar 

  • Joseph, K. C., Stieber, A. &Gonatas, N. K. (1979) Endocytosis of cholera toxin in GERL- like structures of murine neuroblastoma cells pretreated with GM, ganglioside.Journal of Cell Biology 81, 543–54.

    Google Scholar 

  • Keefer, D. A. (1978) Horseradish peroxidase as a retrogradely transported, detailed dendritic marker.Brain Research 140, 15–52.

    Google Scholar 

  • Krieg, W. J. S. (1946) Connections of the cerebral cortex. The albino rat, (B) Structure of the cortical areas.Journal of Comparative Neurology 84, 277–323.

    Google Scholar 

  • Kristensson, K. &Olsson, Y. (1971) Retrograde axonal transport of a protein.Brain Research 29, 363–5.

    Google Scholar 

  • Kristensson, K. &Oesson, Y. (1976) Retrograde transport of horseradish peroxidase in transected axons. 3. Entry into injured axons and subsequent localization in perikaryon.Brain Research 115, 201–13.

    Google Scholar 

  • Lavail, J. H. &Lavail, M. M. (1972) Retrograde axonal transport in the central nervous system.Science 176, 1416–7.

    Google Scholar 

  • Lavail, J. H. &Lavail, M. M. (1974) The retrograde intraaxonal transport of horseradish peroxidase in the chick visual system: A light and electron microscopic study.Journal of Comparative Neurology 157, 303–58.

    Google Scholar 

  • Lavail, J. H., Rapisardi, S. &Sugino, I. K. (1980) Evidence against the smooth endoplasmic reticulum as a continuous channel for the retrograde axonal transport of horseradish peroxidase.Brain Research 191, 3–20.

    Google Scholar 

  • Mesulam, M.-M. (1978) Tetramethyl benzidine 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 

  • Mesulam, M.-M. &Rosene, D. (1979) Sensitivity in horseradish peroxidase neurohistochemistry: A comparative and quantitative study of nine methods.Journal of Histochemistry and Cytochemistry 27, 763–73.

    Google Scholar 

  • Nauta, H. J. W., Kaiserman-Abramof, I. R. &Lasek, R. J. (1975) Electron microscopic observations of horseradish peroxidase transported from caudoputamen to the substantia nigra in the rat: Possible role of the agranular reticulum.Brain Research 85, 373–84.

    Google Scholar 

  • Novikoff, A. B. &Novikoff, P. M. (1977) Cytochemical contributions to differentiating GERL from the Golgi apparatus.Histochemical journal 9, 525–51.

    Google Scholar 

  • Novikoff, P. M., Novikoff, A. B., Quintana, N. &Hauw, J.-J. (1971) Golgi apparatus, GERL, and lysosomes of neurons in rat dorsal root ganglia, studied by thick section and thin section cytochemistry.Journal of Cell Biology 50, 857–86.

    Google Scholar 

  • Ribak, C. E. &Peters, A. (1975) An autoradiographic study of the projections from the lateral geniculate body of the rat.Brain Research 92, 341–68.

    Google Scholar 

  • Rosene, D. S. &Mesulam, M.-M. (1978) Fixation variables in horseradish peroxidase neurohistochemistry. 1. The effects of fixation time and perfusion procedures upon enzyme activity.Journal of Histochemistry and Cytochemistry 26, 28–39.

    Google Scholar 

  • Schwab, M. E. (1977) Ultrastructural localization of nerve growth factor-horseradish peroxidase (NGF-HRP) coupling product after retrograde axonal transport in adrenergic neurons.Brain Research 130, 190–6.

    Google Scholar 

  • Schwab, M. E., Javoy-Agid, F. &Agid, Y. (1978) Labeled wheat germ agglutinin (WGA) as a new, highly sensitive retrograde tracer in the rat brain hippocampal system.Brain Research 152, 145–50.

    Google Scholar 

  • Silverstein, S. C., Steinman, R. M. &Cohn, Z. A. (1977) Endocytosis.Annual Review of Biochemistry 46, 669–722.

    Google Scholar 

  • Staines, W. A., Kimura, H., Fibiger, H. C. &Mcgeer, E. G. (1980) Peroxidase-labeled lectin as a neuroanatomical tracer: Evaluation in a CNS pathway.Brain Research 197, 485–90.

    Google Scholar 

  • Stoeckel, K., Schwab, M. &Thoenen, H. (1977) Role of gangliosides in the uptake and retrograde axonal transport of cholera and tetanus toxin as compared to nerve growth factor and wheat germ agglutinin.Brain Research 132, 273–85.

    Google Scholar 

  • Trojanowski, J. G., Gonatas, J. O. &Gonatas, N. K. (1980) A quantitative comparison of the uptake and retrograde axonal transport of horseradish peroxidase and wheat germ agglutinin-peroxidase conjugates in the visual system of the rat.Journal of Neuropathology and-Experimental Neurology 39, 393 (Abstract).

    Google Scholar 

  • Turner, P. T. &Harris, A. B. (1974) Ultrastructure of exogenous peroxidase in cerebral cortex.Brain Research 74, 305–26.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Trojanowski, J.Q., Gonatas, J.O. & Gonatas, N.K. A light and electron microscopic study of the intraneuronal transport of horseradish peroxidase and wheat germ agglutinin-peroxidase conjugates in the rat visual system. J Neurocytol 10, 441–456 (1981). https://doi.org/10.1007/BF01262415

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01262415

Keywords

Navigation