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. 1984 Nov 1;99(5):1878–1882. doi: 10.1083/jcb.99.5.1878

Calcium transients during early development in single starfish (Asterias forbesi) oocytes

PMCID: PMC2113359  PMID: 6490725

Abstract

Maturation and fertilization of the starfish oocyte are putative calcium-dependent events. We have investigated the spatial distribution and temporal dynamics of this calcium dependence in single oocytes of Asterias forbesi. We used the calcium photoprotein, aequorin, in conjunction with a microscope-photomultiplier and microscope-image intensifier. Surprisingly, in contrast to earlier work with Marasthenias glacialis, there is no detectable increase in intracellular-free calcium in the oocyte of A. forbesi in response to the maturation hormone 1-methyl adenine. During fertilization of the same, matured, A. forbesi oocyte there is a large increase in intracellular-free calcium. The calcium concentration increases to approximately 1 microM at the point of insemination and the region of elevated free calcium expands across the oocyte in approximately 20 s (17-19 degrees C). After the entire oocyte reaches an elevated concentration of free calcium, the concentration decreases uniformly throughout the oocyte over the next several minutes.

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Selected References

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  1. Blinks J. R., Prendergast F. G., Allen D. G. Photoproteins as biological calcium indicators. Pharmacol Rev. 1976 Mar;28(1):1–93. [PubMed] [Google Scholar]
  2. Dorée M., Kishimoto T., Le Peuch C. J., Demaille J. G., Kanatani H. Calcium-mediated transduction of the hormonal message in meiosis reinitiation of starfish oocytes: modulation following injection of cholera toxin and cAMP-dependent protein kinase. Exp Cell Res. 1981 Oct;135(2):237–249. doi: 10.1016/0014-4827(81)90159-2. [DOI] [PubMed] [Google Scholar]
  3. Dorée M., Moreau M., Guerrier P. Hormonal control of meiosis. In vitro induced release of calcium ions from the plasma membrane in starfish oocytes. Exp Cell Res. 1978 Sep;115(2):251–260. doi: 10.1016/0014-4827(78)90279-3. [DOI] [PubMed] [Google Scholar]
  4. Gilkey J. C., Jaffe L. F., Ridgway E. B., Reynolds G. T. A free calcium wave traverses the activating egg of the medaka, Oryzias latipes. J Cell Biol. 1978 Feb;76(2):448–466. doi: 10.1083/jcb.76.2.448. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Kiehart D. P. Studies on the in vivo sensitivity of spindle microtubules to calcium ions and evidence for a vesicular calcium-sequestering system. J Cell Biol. 1981 Mar;88(3):604–617. doi: 10.1083/jcb.88.3.604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Masui Y., Clarke H. J. Oocyte maturation. Int Rev Cytol. 1979;57:185–282. doi: 10.1016/s0074-7696(08)61464-3. [DOI] [PubMed] [Google Scholar]
  7. Meijer L., Guerrier P. Calmodulin in starfish oocytes. I. Calmodulin antagonists inhibit meiosis reinitiation. Dev Biol. 1981 Dec;88(2):318–324. doi: 10.1016/0012-1606(81)90175-5. [DOI] [PubMed] [Google Scholar]
  8. Meijer L., Guerrier P. Calmodulin in starfish oocytes. II. Trypsin treatment suppresses the trifluoperazine-sensitive step. Dev Biol. 1984 Jan;101(1):257–262. doi: 10.1016/0012-1606(84)90139-8. [DOI] [PubMed] [Google Scholar]
  9. Meijer L., Guerrier P. Maturation and fertilization in starfish oocytes. Int Rev Cytol. 1984;86:129–196. doi: 10.1016/s0074-7696(08)60179-5. [DOI] [PubMed] [Google Scholar]
  10. Moreau M., Guerrier P., Doree M., Ashley C. C. Hormone-induced release of intracellular Ca2+ triggers meiosis in starfish oocytes. Nature. 1978 Mar 16;272(5650):251–253. doi: 10.1038/272251a0. [DOI] [PubMed] [Google Scholar]
  11. Picard A., Dorée M. Is calcium the second messenger of 1-methyladenine in meiosis reinitiation of starfish oocytes? Exp Cell Res. 1983 May;145(2):325–337. doi: 10.1016/0014-4827(83)90011-3. [DOI] [PubMed] [Google Scholar]
  12. Reynolds G. T. Image intensification applied to biological problems. Q Rev Biophys. 1972 Aug;5(3):295–347. doi: 10.1017/s0033583500000974. [DOI] [PubMed] [Google Scholar]
  13. SHIMOMURA O., JOHNSON F. H., SAIGA Y. Extraction, purification and properties of aequorin, a bioluminescent protein from the luminous hydromedusan, Aequorea. J Cell Comp Physiol. 1962 Jun;59:223–239. doi: 10.1002/jcp.1030590302. [DOI] [PubMed] [Google Scholar]
  14. Schuetz A. W. Cytoplasmic activation of starfish oocytes by sperm and divalent ionophore A-23187. J Cell Biol. 1975 Jul;66(1):86–94. doi: 10.1083/jcb.66.1.86. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Shimomura O., Shimomura A. EDTA-binding and acylation of the Ca2+-sensitive photoprotein aequorin. FEBS Lett. 1982 Feb 22;138(2):201–204. doi: 10.1016/0014-5793(82)80441-9. [DOI] [PubMed] [Google Scholar]

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