Skip to main content
Log in

Differential frequency of P-cells and I-cells in magnocellular and parvocellular laminae of monkey lateral geniculate nucleus. An ultrastructural study

  • Published:
Experimental Brain Research Aims and scope Submit manuscript

Summary

Acute retrograde ultrastructural changes resulting from complete removal of areas 17, 18 and 19 were used to develop criteria for identification of principal or projective neurons (P-cells) and local interneurons (I-cells) in the dorsal lateral geniculate nucleus (LGNd) of monkeys. Four and six days after axotomy, marked chromatolytic alterations and diminution of rough endoplasmic reticulum were noted in 89 examined neurons of medium or large size, with rich cytoplasmic matrix, large mitochondria, and exhibiting only postsynaptic sites on the perikarya and dendrites. Seventeen other neurons showing no signs of degeneration had a pale matrix, small dense mitochondria and both postsynaptic and presynaptic sites on their perikarya and dendrites. It was concluded that the former group represented P-cells and the latter was characteristic of I-cells.

The morphologic criteria derived from this study were applied to the quantitative analysis of neuronal populations in separate magnocellular and parvocellular laminae. The findings indicate that the latter contain 4.4% of I-cells whereas the former have 15.6% of this neuronal category. The dissimilarity suggests the more preeminent role of I-cells in the magnocellular laminae where they could maintain the transient responses of Y-cells which are known to be the predominant population among the P-cells of these laminae.

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

  • Barron KD, Doolin PF, Oldershaw JB (1967) Ultrastructural observations on retrograde atrophy of lateral geniculate body. J Neuropathol Exp Neurol 26: 300–326

    Google Scholar 

  • Burke W, Sefton AJ (1966) Discharge patterns of principal cells and interneurons in lateral geniculate nucleus of rat. J Physiol (Lond) 187: 201–212

    Google Scholar 

  • Cleland BG, Dubin MS (1976) Interneurons within the lateral geniculate nucleus of the cat. Proc Austr Physiol Pharmacol Soc 7: 468

    Google Scholar 

  • Courten C de, Garey LJ (1982) Morphology of the neurons in the human lateral geniculate nucleus and their normal development. A Golgi study. Exp Brain Res 47: 159–171

    Google Scholar 

  • Dreher B, Fukada Y, Rodieck RW (1976) Identification, classification and anatomical segregation of cells with X-like and Y-like properties in the lateral geniculate nucleus of old-world primates. J Physiol (Lond) 258: 433–452

    Google Scholar 

  • Famiglietti EV Jr., Peters A (1972) The synaptic glomerulus and the intrinsic neuron in the dorsal lateral geniculate nucleus of the cat. J Comp Neurol 144: 285–334

    Google Scholar 

  • Friedlander MJ, Lin CS, Stanford LR, Sherman SM (1981) Morphology of functionally identified neurons in lateral geniculate nucleus of the cat. J Neurophysiol 46: 80–129

    Google Scholar 

  • Guillery RW (1966) A study of Golgi preparations from the dorsal lateral geniculate nucleus of the adult cat. J Comp Neurol 128: 21–50

    Google Scholar 

  • Guillery RW, Colonnier M (1970) Synaptic patterns in the dorsal lateral geniculate nucleus of the monkey. Z Zellforsch 103: 90–108

    Google Scholar 

  • Hámori J, Pasik T, Pasik P, Szentágothai J (1974) Triadic synaptic arrangements and their possible significance in the lateral geniculate nucleus of the monkey. Brain Res 80: 379–393

    Google Scholar 

  • Hámori J, Pasik T, Pasik P (1978) Electron-microscopic identification of axonal initial segments belonging to interneurons in the dorsal lateral geniculate nucleus of the monkey. Neuroscience 3: 403–412

    Google Scholar 

  • Hickey TL, Guillery RW (1981) A study of Golgi preparations from human lateral geniculate nucleus. J Comp Neurol 200: 545–577

    Google Scholar 

  • Lábos E (1977) Theoretical considerations of local neuron circuits and their triadic synaptic arrangements (TSA) in subcortical sensory nuclei. J Neurosci Res 3: 1–10

    Google Scholar 

  • LeVay S (1971) On the neurons and synapses of the lateral geniculate nucleus of the monkey, and the effects of eye enucleation. Z Zellforsch 113: 396–419

    Google Scholar 

  • LeVay S, Ferster D (1977) Relay cell classes in the lateral geniculate nucleus of the cat and the effects of visual deprivation. J Comp Neurol 172: 563–584

    Google Scholar 

  • Lieberman AR (1971) The axon reaction: a review of the principal features of perkaryal responses to axon injury. Int Rev Neurobiol 14: 49–124

    Google Scholar 

  • Lieberman AR (1973) Neurons with presynaptic perikarya and presynaptic dendrites in the rat lateral geniculate nucleus. Brain Res 59: 35–60

    Google Scholar 

  • Lin CS, Kratz KE, Sherman SM (1977) Percentage of relay cells in cat's lateral geniculate nucleus. Brain Res 131: 167–173

    Google Scholar 

  • Marrocco RT, McClurkin JW, Young RA (1982) Spatial summation and conduction latency classification of cells of the lateral geniculate nucleus of macaques. J Neurosci 2: 1275–1291

    Google Scholar 

  • Matthews MA (1973) Death of the central neuron: an electron microscopic study of thalamic retrograde degeneration following cortical ablation. J Neurocytol 2: 265–288

    Google Scholar 

  • Norden JJ, Kaas JH (1978) The identification of relay neurons in the dorsal lateral geniculate nucleus of monkeys using horse-radish peroxidase. J Comp Neurol 182: 707–726

    Google Scholar 

  • O'Leary JL (1940) A structural analysis of the lateral geniculate nucleus of the cat. J Comp Neurol 73: 405–430

    Google Scholar 

  • Osculati F, Gazzanelli G, Marelli M, Franceschini F, Amati S, Cinti S (1980) Critical appraisal of the technique of labeling neurons by retrograde transport of horseradish peroxidase. J Submicrosc Cytol 12: 391–400

    Google Scholar 

  • Pasik P, Pasik T, Hámori J, Szentágothai J (1973) Golgi type II interneurons in the neuronal circuit of the monkey lateral geniculate nucleus. Exp Brain Res 17: 18–34

    Google Scholar 

  • Pasik P, Pasik T, Hámori J (1976) Synapses between interneurons in the lateral geniculate nucleus of monkeys. Exp Brain Res 25: 1–13

    Google Scholar 

  • Polyak S (1957) The vertebrate visual system. Chicago University Press, Chicago

    Google Scholar 

  • Rafols JA, Valverde F (1973) The structure of the dorsal lateral geniculate nucleus in the mouse. A Golgi and electron microscopic study. J Comp Neurol 150: 303–332

    Google Scholar 

  • Ralston HJ III, Chow KL (1973) Synaptic reorganization in the degenerating lateral geniculate nucleus of the rabbit. J Comp Neurol 147: 321–350

    Google Scholar 

  • Saini KD, Garey LJ (1981) Morphology of neurons in the lateral geniculate nucleus of the monkey. A Golgi study. Exp Brain Res 42: 235–248

    Google Scholar 

  • Schiller PH, Malpeli JG (1978) Functional specificity of lateral geniculate nucleus laminae of the rhesus monkey. J Neurophysiol 41: 788–797

    Google Scholar 

  • Sherman SM, Wilson JR, Kaas JH, Webb SV (1976) X- and Y- cells in the dorsal lateral geniculate nucleus of the owl monkey (Aotus trivirgatus). Science 192: 475–476

    Google Scholar 

  • Singer W, Pöppel E, Creutzfeldt O (1972) Inhibitory interaction in the cat's lateral geniculate nucleus. Exp Brain Res 14: 210–226

    Google Scholar 

  • Sumitomo I, Nakamura M, Iwama K (1976) Location and function of the so-called interneurons of the rat lateral geniculate body. Exp Neurol 51: 110–123

    Google Scholar 

  • Szentágothai J (1973) Neuronal and synaptic architecture of the lateral geniculate nucleus. In: Jung R (ed) Central processing of visual information. Handbook of sensory physiology, vol VII/3B. Springer, Berlin Heidelberg New York, pp 141–176

    Google Scholar 

  • Szentágothai J, Hámori J, Tömböl T (1966) Degeneration and electron microscope analysis of the synaptic glomeruli in the lateral geniculate body. Exp Brain Res 2: 283–301

    Google Scholar 

  • Weber AJ, Kalil RE (1982) Percentage of interneurons in the cat's lateral geniculate nucleus. Soc Neurosci Abstr 8: 260

    Google Scholar 

  • Wilson JR, Hendrickson AE (1981) Neuronal and synaptic structure of the dorsal lateral geniculate nucleus in normal and monocularly deprived Macaca monkeys. J Comp Neurol 197: 517–539

    Google Scholar 

  • Winfield DA (1980) The synaptic organization of glomeruli in the magnocellular and parvocellular laminae of the lateral geniculate nucleus. Brain Res 198: 55–62

    Google Scholar 

  • Wong-Riley MTT (1972) Neuronal and synaptic organization of the normal dorsal lateral geniculate nucleus of the squirrel monkey, Saimiri sciureus. J Comp Neurol 144: 25–60

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Aided by NEI Grants Nos. EY-01926 and EY-01867

Rights and permissions

Reprints and permissions

About this article

Cite this article

Hámori, J., Pasik, P. & Pasik, T. Differential frequency of P-cells and I-cells in magnocellular and parvocellular laminae of monkey lateral geniculate nucleus. An ultrastructural study. Exp Brain Res 52, 57–66 (1983). https://doi.org/10.1007/BF00237149

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00237149

Key words

Navigation