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Identification of a distinct synaptic glutamate receptor on horizontal cells in mudpuppy retina

Abstract

The separation of ON and OFF channels and the development of an antagonistic surround occur at the first synapse in the vertebrate retina1–3. This functional differentiation is mediated by the action of the photoreceptor neurotransmitter on the ON bipolar, OFF bipolar and horizontal cells, respectively. Glutamate mimics the action of the photoreceptor transmitter on all second-order neurones in fish4,5, amphibian6 and mammalian7 retinas. The diversity of cellular responses produced by one neurotransmitter raises the possibility of multiple postsynaptic receptor–ionophore complexes. We reported previously that one glutamate analogue, 2-amino-4-phosphonobutyrate, reveals that the ON bipolar synaptic receptor is pharmacologically different from those of other second-order neurones8,9. The results presented here demonstrate that another glutamate analogue, D-O-phosphoserine, selectively antagonizes the synaptic responses of horizontal cells. Taken together, these findings indicate that there are three glutamate-like receptor subtypes in the outer retina and suggest a correlation between receptor subtype and the physiological properties of second-order neurones.

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References

  1. Werblin, F. & Dowling, J. E. J. Neurophysiol. 32, 339–355 (1969).

    Article  CAS  PubMed  Google Scholar 

  2. Kaneko, A. J. Physiol., Lond. 207, 622–633 (1970).

    Article  Google Scholar 

  3. Burkhardt, D. A. J. Physiol., Lond. 236, 593–610 (1974).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  4. Murakami, M., Ohtsu, K. & Ohtsuka, T. J. Physiol., Lond. 227, 889–913 (1972).

    Article  CAS  Google Scholar 

  5. Murakami, M., Ohtsuka, T. & Shimazaki, H. Vision Res. 15, 456–458 (1975).

    Article  CAS  PubMed  Google Scholar 

  6. Slaughter, M. M. & Miller, R. F. J. Neurosci. 3, 1701–1711 (1983).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  7. Bloomfield, S. A. & Dowling, J. E. Soc. Neurosci. Abstr. 8, 131 (1982).

    Google Scholar 

  8. Slaughter, M. M. & Miller, R. F. Science 211, 182–185 (1981).

    Article  CAS  ADS  PubMed  Google Scholar 

  9. Slaughter, M. M. & Miller, R. F. J. Neurosci. (in the press).

  10. Miller, R. F. & Dacheux, R. F. J. gen. Physiol. 67, 639–659 (1976).

    Article  CAS  PubMed  Google Scholar 

  11. Trifonov, J. A. Biofizika 13, 809–814 (1968).

    CAS  PubMed  Google Scholar 

  12. Dowling, J. E. & Ripps, H. Nature 242, 101–103 (1973).

    Article  CAS  ADS  PubMed  Google Scholar 

  13. Dacheux, R. F. & Miller, R. F. Science 191, 963–964 (1976).

    Article  CAS  ADS  PubMed  Google Scholar 

  14. Baylor, D. A., Fuortes, M. G. F. & O'Bryan, P. M. J. Physiol., Lond. 214, 265–294 (1971).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Toyoda, J.-I. & Tonosaki, K. Nature 276, 399–400 (1978).

    Article  CAS  ADS  PubMed  Google Scholar 

  16. O'Bryan, P. M. J. Physiol., Lond. 235, 207–223 (1973).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  17. Attwell, D., Werblin, F. S., Wilson, M. & Wu, S. J. Physiol., Lond. 336, 313–333 (1983).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  18. Skrzypek, J. & Werblin, F. J. Neurophysiol. 49, 1007–1016 (1983).

    Article  CAS  PubMed  Google Scholar 

  19. Slaughter, M. M. & Miller, R. F. Science 219, 1230–1232 (1978).

    Article  ADS  Google Scholar 

  20. Foster, A. C., Fagg, G. E., Harris, E. W. & Cotman, C. W. Brain Res. 242, 374–377 (1982).

    Article  CAS  PubMed  Google Scholar 

  21. Nelson, R. J. Neurophysiol. 36, 519–535 (1973).

    Article  CAS  PubMed  Google Scholar 

  22. Saito, T., Kondo, H. & Toyoda, J. J. gen. Physiol. 73, 73–90 (1979).

    Article  CAS  PubMed  Google Scholar 

  23. Saito, T. & Kaneko, A. J. gen. Physiol. 81, 589–601 (1983).

    Article  CAS  PubMed  Google Scholar 

  24. Ashmore, J. F. & Copenhagen, D. R. Nature 288, 84–86 (1980).

    Article  CAS  ADS  PubMed  Google Scholar 

  25. Ashmore, J. F. & Falk, G. J. Physiol., Lond. 300, 115–150 (1980).

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Copenhagen, D. R., Ashmore, J. F. & Schnapf, J. K. Vision Res. 23, 363–369 (1983).

    Article  CAS  PubMed  Google Scholar 

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Slaughter, M., Miller, R. Identification of a distinct synaptic glutamate receptor on horizontal cells in mudpuppy retina. Nature 314, 96–97 (1985). https://doi.org/10.1038/314096a0

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