Abstract
Glycine and γ-aminobutyric acid (GABA) are inhibitory transmitters of major importance1,2. Whereas neurones using GABA as the transmitter can be visualized by immunocytochemical methods for glutamate decarboxylase (GAD)3,4 or GABA5–8, no comparable techniques have been available for the selective visualization of glycinergic neurones. We have now produced polyclonal antibodies which specifically recognize glycine in glutaral-dehyde-fixed tissue. We used these antibodies to investigate the distribution of glycine in the simple central nervous system (CNS) of the Xenopus embryo, which contains an anatomically and physiologically defined class of reciprocal inhibitory interneurones, the commissural interneurones9–11. These interneurones have an important role in the generation of the swimming motor pattern and are thought to be glycinergic11–13. The glycine antibodies specifically stain these interneurones, revealing their distribution and number in the embryo CNS. This is the first demonstration of the selective localization of glycine-like immunoreactivity in a putative glycinergic class of neurone that has been characterized physiologically, pharmacologically and anatomically.
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References
Curtis, D. R. & Johnston, G. A. R. Ergebn. Physiol. 69, 97–188 (1974).
Krnjević, K. Physiol Rev. 54, 418–540 (1974).
Saito, K. et al. Proc. natn. Acad. Sci. U.S.A. 71, 269–273 (1974).
Mugnaini, E. & Oertel, W. Handbook of Chemical Neuroanatomy Vol. 4 (eds Björklund, A. & Hökfelt, T.) (Elsevier, Amsterdam, 1985).
Storm-Mathisen, J. et al. Nature 301, 517–520 (1983).
Ottersen, O. P. & Storm-Mathisen, J. J. comp. Neurol. 229, 374–392 (1984).
Seguela, P., Geffard, M., Buijs, R. M. & Le Moal, M. Proc. natn. Acad. Sci U.S.A. 81, 3888–3892 (1984).
Hodgson, A., Penke, B., Erdei, A., Chubb, I.W. & Somogyi, P. J. Histochem. Cytochem. 33, 229–239 (1985).
Roberts, A. & Clarke, J. D. W. Phil Trans. R. Soc. B296, 195–212 (1982).
Soffe, S. R., Clarke, J. D. W. & Roberts, A. J. Neurophysiol 51, 1256–1267 (1984).
Dale, N. J. Physiol, Lond. 363, 61–70 (1985).
Roberts, A., Soffe, S. R. & Dale, N. in Neurobiology of Vertebrate Locomotion (eds Grillner, S. et al.) (Macmillan, London, 1986).
Soffe, S. R. J. Physiol, Lond. 382, (1987).
Werman, R., Davidoff, R. A. & Aprison, M. H. Nature 214, 681–683 (1967).
Curtis, D. R., Hösli, L. & Johnston, G. A. R. Expl Brain Res. 6, 1–18 (1968).
Davidoff, R. A., Graham, L. T. Jr., Shank, R. P., Werman, R. & Aprison, M. H. J. Neurochem. 14, 1025–1031 (1967).
Homma, S., Suzuki, T., Murayama, S. & Otsuka, M. J. Neurochem. 32, 691–698 (1979).
Hökfelt, T. & Ljungdahl, Å. Brain Res. 32, 189–194 (1971).
Ljungdahl, Å. & Hökfelt, T. Brain Res. 62, 587–595 (1973).
Matus, A. I. & Dennison, M. E. Brain Res. 32, 195–197 (1971).
Price, D. L., Stocks, A., Griffin, J. W., Young, A. & Peck, K. J. Cell Biol. 68, 389–395 (1976).
Pourcho, R. G. & Goebel, D. J. Brain Res. 348, 339–342 (1985).
Nieuwkoop, P. D. & Faber, J. Normal Tables of Xenopus laevis (Daudin) (North-Holland, Amsterdam, 1956).
Soffe, S. R. & Roberts, A. J. Neurophvsiol. 48, 1279–1288 (1982)
Dale, N., Roberts, A., Ottersen, O. P. & Storm-Mathisen, J. (in preparation).
Madsen, S., Ottersen, O. P. & Storm-Mathisen, J. Neurosci Lett. 60, 255–260 (1985).
Porath, J., Aspberg, K., Drevin, H. & Axén, R. J. Chromatogr. 86, 53–56 (1973).
Hardy, P. M., Nicholls, A. C. & Rydon, H. N. J.C.S. Perkin Trans. 9, 958–962 (1976).
Campistron, G., Buijs, R. M. & Geffard, M. Brain Res. 376, 400–405 (1986).
Ottersen, O. P., Davanger, S. & Storm-Mathisen, J. expl. Brain Res. (in the press).
Ottersen, O. P., Storm-Mathisen, J., Madsen, S., Skumlien, S. & StrøMathisen, J. med. Biol. 64, 147–158 (1986).
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Dale, N., Ottersen, O., Roberts, A. et al. Inhibitory neurones of a motor pattern generator in Xenopus revealed by antibodies to glycine. Nature 324, 255–257 (1986). https://doi.org/10.1038/324255a0
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DOI: https://doi.org/10.1038/324255a0
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