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Distribution and morphology of Alz-50-immunoreactive cells in the developing visual cortex of kittens

  • Published:
Journal of Neurocytology

Summary

The population of interstitial cells of the white matter in the postlateral gyrus of the cat was studied at different postnatal ages using the antibody Alz-50. These neurons are among the first cells to develop in the cortex, and many of them are transitory, disappearing by cell death during the first postnatal days. In the present study, we found that immunoreactivity to Alz-50 is expressed during the first three postnatal weeks, and that positive neurons were not detected after postnatal day (P) 23. In addition to marking cells in the white matter, Alz-50 also recognizes many pyramidal cells in the cortical layers II-III and V of the visual cortex at postnatal day 4. The staining of cortical cells was not observed at other ages. We found that the number of positive cells in the white matter decreases by postnatal days 12 and 16, showing an apparent increase in number at postnatal day 23.

In this study we also attempted to correlate the morphology of Alz-50-immunoreactive cells with the interstitial cells of the white matter, as seen in Golgi preparations. We conclude that Alz-50 immunoreactivity may be related to specific developmental changes and not particularly associated to the occurrence of cell death.

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References

  • Al-Ghoul, W. M. &Miller, M. W. (1989) Transient expression of Alz-50 immunoreactivity in developing rat neocortex: A marker for naturally occurring neuronal death?Brain Research 481, 361–7.

    Google Scholar 

  • Cavanagh, M. E. &Parnavelas, J. G. (1988) Development of somatostatin immunoreactive neurons in the rat occipital cortex: A combined immunocytochemicalautoradiographic study.Journal of Comparative Neurology 268, 1–12.

    Google Scholar 

  • Chun, J. J. M., Nakamura, M. J. &Shatz, C. J. (1987) Transient cells of the developing mammalian telecephalon are peptide immunoreactive neurons.Nature 325, 617–20.

    Google Scholar 

  • Chun, J. J. M. &Shatz, C. (1989a) Interstitial cells of the adult neocortical white matter are the remnant of the early generated subplate neuron population.Journal of Comparative Neurology 282, 555–69.

    Google Scholar 

  • Chun, J. J. M. &Shatz, C. (1989b) The earliest-generated neurons of the cat cerebral cortex: Characterization by MAP2 and neurotransmitter immunohistochemistry during fetal life.Journal of Neuroscience 9, 1648–67.

    Google Scholar 

  • De Carlos, J. A., Lopez-Mascaraque, L. &Valverde, F. (1990) Morphological characterization of Alz-50 immunoreactive cells in the developing neocortex of kittens. InThe Neocortex: Ontogeny and Phylogeny (edited byFinlay, B., Innocenti, G. &Scheich, H.). New York: Plenum Press. NATO Advanced Research Workshop (in press).

    Google Scholar 

  • Foster, G. A. &Schulzberg, M. (1984) Immunohisto-chemical analysis of the ontogeny of neuropeptide Y immunoreactive neurons in the foetal rat brain.International Journal of Developmental Neuroscience 2, 387–407.

    Google Scholar 

  • Ghosh, A., Antonioni, A., Mcconnell, S. K. &Shatz, C. J. (1989) Ablation of subplate neurons alters the development of geniculocortical axons.Society for Neuroscience Abstracts 15, 960.

    Google Scholar 

  • Grundke-Iqbal, I., Ibqal, K., Quinlan, M., Tung, Y.-C., Zaidi, M. S. &Wisniewski, H. M. (1986) Abnormal phosphorylation of the microtubule-associated protein tau in Alzheimer cytoskeletal pathology:Neuroscience Letters 261, 6084–9.

    Google Scholar 

  • Hamre, K. M., Hyman, B. T., Goodlett, C. R., West, J. R. &Van Hoesen, G. W. (1989) Alz-50 immunoreactivity in the neonatal rat: Changes in development and co-distribution with MAP-2 immunoreactivity.Neuroscience Letters 98, 264–71.

    Google Scholar 

  • Huntley, G. W., Hendry, S. H. C., Killackey, H. P., Chalupa, L. M. &Jones, E. G. (1988) Temporal sequence of neurotransmitter expression by developing neurons of fetal monkey visual cortex.Developmental Brain Research 43, 69–96.

    Google Scholar 

  • Hyman, B. T., Van Hoesen, G. W., Wolozin, B. L., Davies, P., Kromer, L. J. &Damasio, A. R. (1988) Alz-50 antibody recognizes Alzheimer-related neuronal changes.Annals of Neurology 23, 371–9.

    Google Scholar 

  • Kostovic, I. &Rakic, P. (1980) Cytology and time of origin of interstitial neurons in the white matter in infant and adult human and monkey telencephalon.Journal of Neurocytology 9, 219–42.

    Google Scholar 

  • Ksiezak-Reding, H., Davies, P. &Yen, S.-H. (1988) Alz-50, a monoclonal antibody to Alzheimer's disease antigen, cross-reacts with tau proteins from bovine and normal humanbrain.Journal of Biological Chemistry 263, 7943–7.

    Google Scholar 

  • Lund, J. S., Lund, R. D., Hendrikson, A. E., Bunt, A. H. &Fuchs, F. (1975) The origin of efferent pathways from the primary visual cortex, area 17, of the macaque monkey as shown by retrograde transport of horseradish peroxidase.Journal of Comparative Neurology 164, 287–304.

    Google Scholar 

  • Lund, R. D. &Mustari, M. J. (1977) Development of the geniculocortical pathway in rats.Journal of Comparative Neurology 173, 289–306.

    Google Scholar 

  • Luskin, M. B. &Shatz, C. (1985) Studies of the earliest generated cells of the cat's visual cortex: Cogeneration of subplate and marginal zones.Journal of Neuroscience 5, 1062–75.

    Google Scholar 

  • McConnell, S. K., Ghosh, A. &Shatz, C. J. (1989) Subplate neurons pioneer the first axon pathway from the cerebral cortex.Science 245, 978–82.

    Google Scholar 

  • Naus, C. C., Miller, F. D., Morrison, J. H. &Bloom, F. E. (1988) Immunohistochemical and in situ hybridization analysis of the development of the rat somatostatin-containing neocortical neuronal system.Journal of Comparative Neurology 269, 448–63.

    Google Scholar 

  • Raedler, E. &Raedler, A. (1978) Autoradiographic study of early neurogenesis in rat neocortex.Anatomy and Embryology 154, 267–84.

    Google Scholar 

  • Rakic, P. (1977) Prenatal development of the visual system in rhesus monkey.Philosophical Transactions of the Royal Society, London, B 278, 245–60.

    Google Scholar 

  • Rickmann, M., Chronwall, B. M. &Wolff, J. R. (1977) On the development of non-pyramidal neurons and axons outside the cortical plate: The early marginal zone as a palliai anlage.Anatomy and Embryology 151, 285–307.

    Google Scholar 

  • Selkoe, D. J. (1989) Biochemistry of altered brain proteins in Alzheimer's disease.Annual Review of Neuroscience 12, 463–90.

    Google Scholar 

  • Shatz, C. J. &Luskin, M. B. (1986) The relationship between the geniculocortical afferents and their cortical target cells during development of the cat's primary visual cortex.Journal of Neuroscience 6, 3655–68.

    Google Scholar 

  • Valverde, F. (1970) The Golgi method. A tool for comparative structural analyses. InContemporary Research Methods in Neuroanatomy (edited byNauta, W. J. H. &Ebbesson, S. O. E.)pp. 12–31. Berlin: Springer Verlag.

    Google Scholar 

  • Valverde, F. &Facal-Valverde, M. V. (1987) Transitory population of cells in the temporal cortex of kittens.Developmental Brain Research 32, 283–8.

    Google Scholar 

  • Valverde, F. &Facal-Valverde, M. V. (1988) Postnatal development of interstitial (subplate) cells in the white matter of the temporal cortex of kittens. A correlated Golgi and electron microscopic study.Journal of Comparative Neurology 269, 168–92.

    Google Scholar 

  • Valverde, F., Facal-Valverde, M. V., Santacana, M. &Heredia, M. (1989) Development and differentiation of early generated cells of sublayer VIb in the somatosensory cortex of the rat: A correlated Golgi and autoradiographic study.Journal of Comparative Neurology 290, 118–40.

    Google Scholar 

  • Wahle, P. &Meyer, G. (1987) Morphology and postnatal changes of transient NPY-ir neuronal populations during early postnatal development of the cat visual cortex.Journal of Comparative Neurology 261, 165–95.

    Google Scholar 

  • Wahle, P. &Meyer, G. (1989) Early postnatal development of vasoactive intestinal polypeptide- and peptide histidine isoleucine-immunoreactive structures in the cat visual cortex.Journal of Comparative Neurology 282, 215–48.

    Google Scholar 

  • Wise, S. P. &Jones, E. G. (1978) Developmental studies of thalamocortical and commissural connections in the rat somatic sensory cortex.Journal of Comparative Neurology 175, 187–208.

    Google Scholar 

  • Wolff, J. R., Bottcher, H., Zetzshe, T., Oertel, W. H. &Chronwall, B. M. (1984) Development of GABAergic neurons in rat visual cortex as identified by glutamate decarboxylase-like immunoreactivity.Neurosdence Letters 47, 207–12.

    Google Scholar 

  • Wolozin, B. L., Pruchnicki, A., Dickson, D. W. &Davies, P. (1986) A neuronal antigen in the brains of Alzheimer patients.Science 232, 648–50.

    Google Scholar 

  • Wolozin, B. L., Scicutella, A. &Davies, P. (1988) Reexpression of a developmentally regulated antigen in Down syndrome and Alzheimer disease.Proceedings of the National Academy of Sciences (USA) 85, 6202–6.

    Google Scholar 

  • Woodhams, P. L., Allen, Y. S., McGovern, J., Allen, J. M., Bloom, S. R., Balazs, R. &Polak, J. M. (1985) Immunohistochemical analysis of the early ontogeny of the neuropeptide Y system in rat brain.Neuroscience 15, 173–202.

    Google Scholar 

  • Wood, J. G., Mirra, S. S., Pollock, N. J. &Binder, L. I. (1986) Neurofibrillary tangles of Alzheimer disease share antigenic determinants with the axonal microtubuleassociated protein tau.Proceedings of the National Academy of Sciences (USA) 83, 4040–3.

    Google Scholar 

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Valverde, F., Lopez-Mascaraque, L. & De Carlos, J.A. Distribution and morphology of Alz-50-immunoreactive cells in the developing visual cortex of kittens. J Neurocytol 19, 662–671 (1990). https://doi.org/10.1007/BF01188035

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