Skip to main content
Log in

Comparative morphometry of Bergmann glial (Golgi epithelial) cells

A Golgi study

  • Original Articles
  • Published:
Anatomy and Embryology Aims and scope Submit manuscript

Summary

Bergmann glial (Golgi epithelial) cells were Golgi-impregnated in the cerebella of species with great differences in the thickness of the molecular layer, in small African native mouse, rat, rhesus monkey, and man. The thickness of the molecular layer determines the length of the radial Bergmann cell processes. Whereas the overall morphology of the cells was found to be strikingly similar in all species studied, there were great quantitative differences in length and diameter of the stem processes. Species with thick molecular layers (man, monkey) have thicker stem processes than species with short distances between Bergmann glial cell soma and pial surface (rat, mouse). This could mean that larger animals with longer gestation periods allow for prolonged growth of cell volumes. On the other hand, an increase in the diameter of long processes should reduce the cytoplasmic resistance against ionic currents; this would be important when Bergmann glial cells — like retinal Müller cells — would act as “cables” for spatial buffering of potassium ions released by electrically active neurons. By contrast, the fractal dimension — i.e., a quantitative measure of the complexity of the cell's border of the cell processes was lower in species with long processes. In an age series of rat cells, the fractal dimension is shown to increase slightly up to a very old age.

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

  • Braitenberg V, Guglielmotti V, Sada E (1967) Correlation of crystal growth with the staining of axons by the Golgi procedure. Stain Technol 42:277–283

    Google Scholar 

  • Flook AG (1978) The use of dilation logic on the quantimet to achieve fractal dimension characterisation of textured and structured profiles. Powder Technol 21:295–298

    Google Scholar 

  • Futamachi KJ, Mutani R, Prince DA (1974) Potassium activity in rabbit cortex. Brain Res 75:5–25

    Google Scholar 

  • Gardner-Medwin AR (1984) A foot in the vitreous fluid. Nature 309:113

    Google Scholar 

  • Hanke S, Reichenbach A (1987) Quantitative-morphometric aspects of Bergmann glial (Golgi epithelial) cell development in rats. Anat Embryol 177:183–188

    Google Scholar 

  • Harris RM (1985) Light microscopic depth measurements of thick sections. J Neurosci Methods 14:97–100

    Google Scholar 

  • Kocsis JD (1986) Functional characteristics of potassium channels of normal and pathological mammalian axons. In: Richtie JM, Keynes RD, Bolis R (eds) Neurology and neurobiology, vol 20, Ion channels in Neural Membranes. Liss, New York, pp 123–144

    Google Scholar 

  • Lange W (1976) The myelinated parallel fibres of the cerebellar cortex and their regional distribution. Cell Tissue Res 166:489–496

    Google Scholar 

  • Mandelbrot BB (1982) The fractal geometry of nature. Freeman, New York

    Google Scholar 

  • Mugnaini E (1972) The histology and cytology of the cerebellar cortex. In: Larsell O, Jansen J (eds) The comparative anatomy and histology of the cerebellum. University of Minnesota Press, Minnesota, pp 201–264

    Google Scholar 

  • Mutani R, Futamachi KJ, Prince DA (1974) Potassium activity in immature cortex. Brain Res 75:27–39

    Google Scholar 

  • Newman EA (1984) Regional specialization of retinal glial cell membrane. Nature 309:155–157

    Google Scholar 

  • Newman EA (1986) High potassium conductance in astrocyte end-feet. Science 223:453–454

    Google Scholar 

  • Newman EA, Frambach DA, Odette LL (1984) Control of extracellular potassium levels by retinal glial cell K+ siphoning. Science 225:1174–1175

    Google Scholar 

  • Pouwels E (1978) On the development of the cerebellum of the trout, Salmo gairdeneri. V. Neuroglial cell development Anat Embryol 3:67–83

    Google Scholar 

  • Rall W (1977) Core conductor theory and cable properties of neurons. In: Brookhart JM, Mountcastle VB (eds) Handbook of physiology, Sect 1: The Nervous System, vol 1, Cellular biology of neurons, Part 1. Am Physiol Soc, Bethesda, pp 39–97

    Google Scholar 

  • Ramon y Cajal S (1955) Histologie du Système Nerveux de l'Homme et des Vertébrés. CSIC Madrid (Reprint of 1909–1911 edn)

    Google Scholar 

  • Reichelt W, Dettmer D, Brückner G, Brust P, Eberhardt W, Reichenbach A (1989) Potassium as a signal for both proliferation and differentation of rabbit retinal (Müller) glial cells growing in cell culture. Cell Signaling 1:187–194

    Google Scholar 

  • Reichenbach A (1989) Attempt to classify glial cells by means of their process specialization using the rabbit retinal Müller cells as an example of cytotopographic specialization of glial cells. Glia 2:250–259

    Google Scholar 

  • Reichenbach A, Reichelt W (1986) Postnatal development of radial glial (Müller) cells of the rabbit retina. Neurosci Lett 71:125–130

    Google Scholar 

  • Reichenbach A, Neumann M, Brückner G (1987) Cell length to diameter relation of rat fetal radial glia — does impaired K+ transport capacity of long thin cells cause their perinatal transformation into multipolar astrocytes? Neurosci Lett 73:95–100

    Google Scholar 

  • Reichenbach A, Schneider H, Leibnitz L, Reichelt W, Schaaf P, Schümann R (1989) The structure of rabbit retinal Müller (glial) cells is adapted to the surrounding retinal layers. Anat Embryol 180:71–79

    Google Scholar 

  • Sacher GA, Staffelt EF (1974) Relation of gestation time to brain weight for placental mammals: implications for the theory of vertebrate growth. Am Nat 108:593–615

    Google Scholar 

  • Senitz D, Goertchen R (1978) Über Astrozytenveränderungen in der orbitofrontalen Hirnrinde bei seniler Demenz. Zentralbl Allg Pathol 122:515–521

    Google Scholar 

  • Smith TG Jr, Marks WB, Lange GD, Sheriff WH Jr, Neale EA (1989) A fractal analysis of cell images. J Neurosci Methods 27:173–180

    Google Scholar 

  • Smith TG Jr, Behar TN, Lange GD, Marks WB, Sheriff WH Jr (1991) A fractal analysis of cultured rat optic nerve glial growth and differentiation. Neuroscience 41:159–169

    Google Scholar 

  • Somjen GG (1978) Metabolic and electrical correlates of the clearing of excess potassium in the cortex and spinal cord. In: Porter A (ed) Studies in neurophysiology. Cambridge University Press, Cambridge, pp 181–201

    Google Scholar 

  • Stolzenburg J-U, Reichenbach A, Neumann M (1989) Size and density of glial and neuronal cells within the cerebral neocortex of various insectivorian species. Glia 2:78–84

    Google Scholar 

  • Syková E (1981) Extracellular K+ accumulation in the spinal cord. In: Syková E, Hnik P, Vyklicky L (eds) Ion-selective microelectrodes and their use in excitable tissues. Plenum Press, New York London, pp 139–158

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Siegel, A., Reichenbach, A., Hanke, S. et al. Comparative morphometry of Bergmann glial (Golgi epithelial) cells. Anat Embryol 183, 605–612 (1991). https://doi.org/10.1007/BF00187909

Download citation

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00187909

Key words

Navigation