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Monomeric and polymeric forms of ependymin: A brain extracellular glycoprotein implicated in memory consolidation processes

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Abstract

Ependymin, a brain extracellular glycoprotein that appears to be implicated in neural circuit modifications associated with the process of memory consolidation, can rapidly polymerize into fibrous aggregates when the Ca2+ concentration in solution is reduced by the addition of EGTA or by dialysis. Such aggregates, once formed, could not be redissolved in boiling 1% SDS in 6 M urea, acetic acid, saturated aqueous potassium thiocyanate, and trifluoroacetic acid. They were, however, soluble in formic acid. Investigations of the immunological properties of ependymin indicated that various monomers, oligomers and polymers of the molecule with differing carbohydrate contents can be obtained. The polymerization properties of the ependymins may play an important role in their functions in memory consolidation mechanisms.

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References

  1. Hydén, H. V., and Egyházi E. 1962. Nuclear RNA changes of nerve cells during a learning experiment in rats. Proc. Natl. Acad. Sci. USA 48:1366–1373.

    Google Scholar 

  2. Flexner, J. B., Flexner, L. D., Stellar, E., de la Haba, G., and Roberts, R. B. 1962. Protein synthesis in brain and learning and memory following puromycin. J. Neurochem. 9:595–605.

    Google Scholar 

  3. Agranoff, B. W., Davis, R. E., and Brink, J. J. 1967. Memory fixation in the goldfish. Proc. Natl. Acad. Sci. USA 54:788–793.

    Google Scholar 

  4. Barondes, S. H., and Cohen, H. D. 1967. Comparative effects of cyclohexamide and puromycin on cerebral protein synthesis and consolidation of memory in mice. Brain Res. 4:44–51.

    Google Scholar 

  5. Shashoua, V. E. 1968. RNA changes in goldfish brain during learning. Nature 217:238–240.

    Google Scholar 

  6. Alkon, D. L. 1980. Cellular analysis of a gastropod (Hermissenda crassicornis) model of associative learning. Biol. Bull. 159:505–560.

    Google Scholar 

  7. Carew, T. L., Walters, E. T., and Kandell, C. R. 1981. Associative learning inAplysia: Cellular correlates supporting a conditioned fear hypothesis. Science 211:501–504.

    Google Scholar 

  8. Thompson, R. F., Berger, T. W., and Madden, J. 1983. Cellular processes of learning and memory in the mammalian CNS. Ann. Rev. Neurosci. 6:447–492.

    Google Scholar 

  9. West, R. W., and Greenough, W. G. 1972. Effect of environmental complexity on cortical synapses of rats: Preliminary results. Behav. Biol. 7:279–284.

    Google Scholar 

  10. Mollgaard, V., Diamond, M. D., Bennett, E. L., Rosenzweig, M. R., and Linder, B. 1971. Quantitative synaptic changes with differential experience in rat brain. Intl. J. Neurosci. 2:113–128.

    Google Scholar 

  11. Lynch, G. S., and Schubert, P. 1980. The use of in vitro brain slices for multidisciplinary studies of synaptic function. Ann Rev. Neurosci. 3:1–22.

    Google Scholar 

  12. Duffy, C., Teyler, T. J., and Shashoua, V. E. 1981. Long-term potentiation in the hippocampal slice: Evidence for stimulated secretion of newly synthesized proteins. Science 212:1148–1151.

    Google Scholar 

  13. Shashoua, V. E. 1976. Identification of specific changes in the pattern of brain protein synthesis after training. Science 193:1264–1266.

    Google Scholar 

  14. Shashoua, V. E., and Moore, M. E. 1978. Effect of antisera to β and γ goldfish brain proteins on the retention of a newly acquired behavior. Brain Res. 148:441–449.

    Google Scholar 

  15. Schmidt, R. 1985. Involvement and function of specific goldfish brain glycoproteins (ependymins) in two different learning paradigms. J. Neurochem. 44S:21.

    Google Scholar 

  16. Benowitz, L. I., and Shashoua, V. E. 1977. Localization of a brain protein metabolically linked with behavioral plasticity in the goldfish. Brain Res. 136:227–242.

    Google Scholar 

  17. Shashoua, V. E. 1979. Brain metabolism and the acquisition of new behaviors. III. Evidence for secretion of two proteins into the brain extracellular fluid after training. Brain Res. 166:349–358.

    Google Scholar 

  18. Shashoua, V. E., Daniel, P. F., Moore, M. E., and Jungalwala, F. B. 1986. Demonstration of glucuronic acid on brain glycoproteins which react with HNK-1 antibody. Biochem. Biophys. Res. Comm. 138:902–909.

    Google Scholar 

  19. Shashoua, V. E. 1985. The role of brain extracellular proteins in neuroplasticity and learning. Cell. Molec. Neurobiol. 5:183–207.

    Google Scholar 

  20. Shashoua, V. E. 1981. Extracellular fluid proteins of goldfish brain: Studies of concentration and labeling patterns. Neurochem. Res. 6:1129–1147.

    Google Scholar 

  21. Shashoua, V. E., and Holmquist, B. 1986. Extracellular fluid proteins of goldfish brain: Evidence for the presence of proteases and esterases. J. Neurochem. 47:738–743.

    Google Scholar 

  22. Shashoua, V. E. 1977. Brain metabolism and the acquisition of new behaviors. II. Immunological studies of the α, β and γ proteins of goldfish brain. Brain Res. 122:113–124.

    Google Scholar 

  23. Schmidt, R., and Shashoua, V. E. 1981. A radioimmunoassay for ependymins β and γ: Two goldfish brain proteins involved in behavioral plasticity. J. Neurochem. 36:1368–1377.

    Google Scholar 

  24. Laemmli, U. K. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227:680–685.

    Google Scholar 

  25. O'Farrell, P. H. 1975. High resolution of two-dimensional electrophoresis of proteins. J. Biol. Chem. 250:4007–4021.

    Google Scholar 

  26. Oakley, B. R., Kirsch, D. R., and Morris, N. R. 1980. A simplified ultrasensitive silver stain for detecting proteins in polyacrylamide gels. Analyt. Biochem. 105:361–363.

    Google Scholar 

  27. McGarry, R. C., Helfand, S. L., Quarles, R. H., and Roder, J. C. 1983. Recognition of myelin-associated glycoprotein by the monoclonal antibody HNK-1. Nature 306:376–378.

    Google Scholar 

  28. Towbin, H., Staehelin, T., and Gordon, J. 1979. Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: Procedure and some applications. Proc. Natl. Acad. Sci. USA 76:4350–4354.

    Google Scholar 

  29. Sternberger, L. A. 1979. Immunochemistry. J. Wiley & Sons, New York.

    Google Scholar 

  30. Bradford, M. M. 1976. A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Analyt. Biochem. 72:248–254.

    Google Scholar 

  31. Plummer, T. H., Elder, J. H., Alexander, S., Phelan, A. W., and Tarentino, A. L. 1984. Demonstration of peptide: N-glycosidase F activity in endo-β-N-acetylglucosaminidase F preparations. J. Biol. Chem. 259:10700–10704.

    Google Scholar 

  32. Cserr, H. F., and Ostrach, L. H. 1974. On the presence of subarachnoid fluid in the mudpuppy,Necturus maculosus. Comp. Biochem. Physiol. 48A:145–151.

    Google Scholar 

  33. Schmidt, R., and Shashoua, V. E. 1983. Structural and metabolic relationships between goldfish brain glycoproteins participating in functional plasticity of the central nervous system. J. Neurochem. 40:652–660.

    Google Scholar 

  34. Shelanski, M. L., Gaskin, F., and Cantor, C. R. 1973. Microtubule assembly in the absence of added nucleotides. Proc. Natl. Acad. Sci. USA 70:765–768.

    Google Scholar 

  35. Truding, R., Shelanski, M. L., and Morell, P. 1975. Glycoproteins released into culture medium of differentiating murine neuroblastoma cells. J. Biol. Chem. 250:9348–9354.

    Google Scholar 

  36. Macklin, W. B., and Lees, M. B. 1982. Solid phase immunoassays for quantitation of antibody to bovine white matter proteolipid apoprotein. J. Neurochem. 38:348–355.

    Google Scholar 

  37. Timasheff, S. N. 1981. Pages 315–336,in Frieden, C., and Nichol, W. W. (eds.), Protein-protein interactions, J. Wiley & Sons, New York.

    Google Scholar 

  38. Krnjević, K., Morris, M. E., and Reiffenstein, R. J. 1982. Stimulation-evoked changes in extracellular K+ and Ca+ concentration in pyramidal layers of the rat's hippocampus. Can. J. Physiol. Pharmacol. 60:1643–1657.

    Google Scholar 

  39. Somjen, G. G. 1980. Stimulus-evoked and seizure-related responses of extracellular calcium activity in spinal cord compared to those in cerebral cortex. J. Neurophysiol. 44:617–632.

    Google Scholar 

  40. Morris, M. E., Ropert, N., and Shashoua, V. E. 1986. Stimulus evoked changes in extracellular Ca2+ in optic tectum of goldfish. Ann. N.Y. Acad. Sci. 481:375–377.

    Google Scholar 

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Special Issue dedicated to Prof. Holger Hydén.

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Shashoua, V.E. Monomeric and polymeric forms of ependymin: A brain extracellular glycoprotein implicated in memory consolidation processes. Neurochem Res 13, 649–655 (1988). https://doi.org/10.1007/BF00973283

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