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Nature 286, 185 - 186 (10 July 1980); doi:10.1038/286185a0

Calcium-induced decrease in membrane fluidity of sea urchin egg cortex after fertilization

Judith Campisi* & Carl J. Scandella

Department of Biochemistry, State University of New York, Stony Brook, New York 11794
*Present address: Laboratory of Tumor Biology, Sidney Farber Cancer Institute, 44 Binney Street, Boston, Massachusetts 02115.

Fertilization of the sea urchin egg is a dramatic example of cell activation resulting from the interaction of an external stimulus, the spermatozoon, with the cell surface1. Growing and quiescent cells may have different membrane states2. Here we report membrane fluidity measurements on a surface membrane fraction, the cortex, isolated from unfertilized and fertilized eggs. The fluidity of the fertilized egg cortex, measured by electron spin resonance (ESR) spectroscopy using 5-doxy 1st ear at e as a probe, is less than that of the unfertilized cortex. In the intact egg the intracellular Ca2+ concentration increases after fertilization and this transient rise seems to be localized in the cortex3. The addition of Ca2+ to the cortex fraction isolated from unfertilized eggs triggers a fluidity decrease in vitro. The fluidity decrease seems to represent a Ca2+-induced change in membrane structure rather than a direct interaction of Ca2+ with phospholipid headgroups.

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References
1. Epel, D. Curr. Topics dev. Biol. 12, 186−292 (1978).
2. Pardee, A. B., de Asua, J. & Rosengurt, E. in Control of Proliferation in Animal Cells (eds Clarkson, B. & Baserga, R.) 547−561 (Cold Spring Harbor, New York, 1974). | ChemPort |
3. Steinhardt, R., Zucker, R. & Schatten, G. Devl Biol. 58, 185−196 (1977). | ChemPort |
4. Campisi, J. & Scandella, C. J. Science 199, 1336−1337 (1978). | PubMed | ISI | ChemPort |
5. Campisi, J. & Scandella, C. J. J. biol. Chem. (in the press).
6. Vacquier, V. D. Devl Biol. 43, 62−74 (1975). | ChemPort |
7. Schatten, G. & Mazia, D. Expl Cell Res. 98, 325−337 (1976). | ChemPort |
8. Detering, N. K., Decker, G. L., Schmell, E. D. & Lennarz, W. J. J. Cell Biol. 75, 899−914 (1977). | Article | PubMed | ISI | ChemPort |
9. Grainger, J. thesis, Univ. California (1978).
10. Schuel, H. Gamete Res. 1, 299−382 (1978). | ISI |
11. Citkowitz, E. Devl Biol. 24, 348−362 (1971). | ChemPort |
12. Schroeder, T. E. J. Cell Biol. 79, 171a (1979).
13. Gaffney, B. J. Meth. Enzym. 32B, 161−198 (1974). | Article | PubMed | ChemPort |
14. Chapman, D. Q. Rev. Biophys. 8, 185−235 (1975). | ChemPort |
15. McLaughlin, S. Curr. Topics Membrane Transport 9, 71−144 (1977). | ChemPort |
16. Johnson, M. & Edidin, M. Nature 272, 448−450 (1978). | PubMed | ISI | ChemPort |
17. Hiramoto, Y. Expl Cell Res. 89, 320−326 (1974). | ChemPort |
18. Sinensky, M., Pinkerton, F., Sutherland, E. & Simon, F. R. Proc. natn. Acad. Sci. U.S.A. 76, 4893−4897 (1979). | ChemPort |
19. Klein, I., Moore, L. & Pastan, I. Biochim. biophys. Acta 506, 42−53 (1978). | Article | PubMed | ISI | ChemPort |
20. Paul, M. & Epel, D. Expl Cell Res. 65, 281−288 (1971). | ChemPort |
21. Kalb, V. F. & Bernlohr, R. W. Analyt. Biochem. 82, 362−371 (1977). | PubMed | ISI | ChemPort |
22. Wharton, D. C. & Tzagoloff, A. Meth. Enzym. 10, 245−250 (1967). | Article | ChemPort |
23. Avruch, J. & Wallach, D. F. H. Biochim. biophys. Acta 233, 334−347 (1971). | Article | PubMed | ISI | ChemPort |



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