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Long-term effects of brain trypsinization before cell seeding on cell morphology and surface composition

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Abstract

The relation between the pattern of proteins localized in the surface of astroglial cells and cell differentiation was investigated in primary cultures derived from neonatal rat brains, dissociated either mechanically (MDC) or by 3 (TDC3) and 30 minutes (TDC30) trypsinization. Morphological and ultrastructural studies revealed a bed layer composed of flat, polygonal young and differentiated astrocytes in all types of cultures and a surface layer composed of small, ovoide undifferentiated cells which were more numerous in TDC30 than in TDC3 and MDC. The enrichment in undifferentiated cells, induced by prolonged brain trypsinization prior cell seeding, was observed during two weeks in culture: latter, by day 20, the cell population in all cultures was that of differentiated astrocytes. The presence of structural and enzymatic cell markers indicated that the cell population in MDC and TDC3 as well as in TDC30, including the small cells, was of astroglial origin. Concomitant with the morphological changes, cells in TDC30 were less accessible to surface labeling than those composing MDC. Subsequent electrophoresis of the labeled surface proteins demonstrated that a 140–130 K complex was the most “sensible” to brain trypsinization and that their accessibility to the surface probing was maximal during the differentiation of astrocytes in MDC or of small cells in TDC30. By day 20, these components were not significantly labeled in both, MDC, and TDC30, cultures. The use of two types of astrocytes primary culture which were different in the ratio of differentiated to undifferentiated cells and their surface labeling at different growth stages showed a variation in the composition of surface proteins during the cell maturation. The increased accessibility of some surface proteins to external probing when the cells developed to differentiated astrocytes might suggest their involvement in cell differentiation.

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References

  1. Mautner, V., andHynes, R. O. 1977. Surface distribution of LETS protein in relation to the cytoskeleton of normal and transformed cells. J. Cell Biol. 75:743–768.

    PubMed  Google Scholar 

  2. Stocker, M. G. P., andRubin, H. 1967. Density dependent inhibition of cell growth in culture. Nature 215:171–172.

    PubMed  Google Scholar 

  3. Nelson, N. H. Teng, andLan Bo Chen. 1975. The role of surface proteins in cell proliferation as studied with thrombin and other proteases. Proc. Natl. Acad. Sci. 72:413–417.

    PubMed  Google Scholar 

  4. Darrel, H. C., andCunningham, D. D. 1977. Initiation of chick cell division by trypsin action of the cell surface. Nature 268:602–606.

    PubMed  Google Scholar 

  5. Darrell, H. C., andCunningham, D. D. 1978. Cell surface actionof thrombin is sufficient to initiate division of chick cells. Cell 14:811–823.

    PubMed  Google Scholar 

  6. Kleinschuster, S. J., andMoscona, A. A. 1972. Interaction of embryonic and fetal neural retina cells with carbohydrate-binding phytoagglotinins: Cell Surface Changes with Differentiation. Exp. Cell. Res. 70:397–410.

    PubMed  Google Scholar 

  7. Mintz, G., andGlaser, L. 1978. Specific glycoprotein changes during development of the chick neural retina. J. Cell Biol. 79:132–137.

    PubMed  Google Scholar 

  8. Zanetta, J. P., Roussel, G., Ghandour, M. S., andGombos, G. 1978. Postnatal development of rat cerebellum: massive and transient accumulation of concanavalin A binding glycoproteins in parallel fiber axolema. Brain Res. 142:301–319.

    PubMed  Google Scholar 

  9. Sensenbrenner, M. Devilliers, G., Bock, E., andPorte, A. 1980. Biochemical and ultrastructural studies of cultured rat astroglial cells. Differentiation 17:51–61.

    PubMed  Google Scholar 

  10. Neskovic, N. M., Sarlieve, L. L., andMandel, P. 1974. Purification and properties of UDP-galactose: ceramide galactosyltransferase from rat brain microsomes. Biochim. Biophys. Acta 334:309–315.

    Google Scholar 

  11. Marangos, P. J., Goodwin, K., Parma, R., Lauter, R., andTrans, E. 1978. Neuron specific protein (NSP) in neuroblastoma cells: Relation to differentiation. Brain Res. 145:49–58

    PubMed  Google Scholar 

  12. Delaunoy, J. P., Hog, F., Devilliers G., Bansart, M., Mandel, P., andSensenbrenner, M. 1979. Developmental changes and localization of carbonic anhydrase in cerebral hemispheres of the rat and in rat glia cell cultures. Cell. Mol. Biol. 26:235–240.

    Google Scholar 

  13. Delaunoy, J. P., Filippi, G., Laurent, G., andMandel, P. 1978. Quantitative measurements of carbonic anhydrase (CAII) in the central nervous system of neurological mutant mice “Jimpy” by radioimmunoassay. Brain Res. 155:201–204.

    PubMed  Google Scholar 

  14. Lowry, O. H., Rosebrough, N. J., Farr, A. L., andRandall, R. J. 1951. Protein measurement with the phenol reagent. J. Biol. Chem. 193:265–175.

    PubMed  Google Scholar 

  15. Benenson, A., Kapeller, K. A., andDoljanski, F. 1977. Surface proteins of fibroblasts and sarcoma cells. Their shedding and trypsin susceptibility. Is. J. Med. Sci. 13:852–858.

    Google Scholar 

  16. Plesser, Y. M., Weiss, D. W., andDoljanski, F. 1980. Cell surface shedding by fibroblasts in culture. Is. J. Med. Sci. 16:519–529.

    Google Scholar 

  17. Sensenbrenner, M., Labourdette, G., Delaunoy, J. P., Pettamnn, B., Devilliers, G., Moonen, G., andBock, E. 1980. Morphological and biochemical differentiation of glial cells in primary culture. Tissue Culture in Neurobiologyin Giacobini, E., Vernadakis, A., andShahar, A. (eds.), Raven Press, New York.

    Google Scholar 

  18. Bornstein, P., andAsh, J. F. 1977. Cell surface-associated structural proteins in connective tissue cells. Proc. Natl. Acad. Sci. 74:2480–2484.

    PubMed  Google Scholar 

  19. Yamamoto, K., Yamamoto, M., andOoka, H. 1977. Cell surface changes associated with aging of chick embryo fibroblasts in culture. Exp. Cell Res. 108:87–93.

    PubMed  Google Scholar 

  20. Sieber-Blum, M., andCohen, A. M., 1978. Lectin binding to neural crist cells. Changes of the cell surface during differentiation in vitro. J. Cell. Biol. 76:628–638.

    PubMed  Google Scholar 

  21. Maylié-Pfenninger, M. F., andJaniesson, J. D. 1980. Development of cell surface saccharides in embryonic pancreatic cells. J. Cell Biol. 86:96–103.

    PubMed  Google Scholar 

  22. Mersel, M., Benenson, A., andDoljanski, F. 1976. Lactoperoxidase-catalyzed radioiodination of surface membrane lipids. Biochem. Biophys. Res. Commun. 70:1166–1171.

    PubMed  Google Scholar 

  23. Gross, Z., andRottem, S. 1979. Lipid distribution in achole plasma Laidlawii membrane. A study using the lactoperoxidase mediated iodination. Biochim. Biophys. Acta 555:547–542.

    PubMed  Google Scholar 

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Mersel, M., Benenson, A., Delaunoy, J.P. et al. Long-term effects of brain trypsinization before cell seeding on cell morphology and surface composition. Neurochem Res 8, 449–463 (1983). https://doi.org/10.1007/BF00965101

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