Cortical granule translocation during maturation of starfish oocytes requires cytoskeletal rearrangement triggered by InsP3-mediated Ca2+ release

Experimental Cell Research

Volumn 248, Issue 2, 1999, Pages 567-574

  Santella, Luigia ^a   De Riso, Laura ^a   Gragnaniello, Giovanni ^a   Kyozuka, Keiichiro ^b  

^a STAZIONE ZOOLOGICA ANTON DOHRN   (Italy)

^b TOHOKU UNIVERSITY   (Japan)

Author keywords

Cortical granules reaction; Cytoskeleton; InsP3 receptors; Meiotic maturation; Starfish oocyte

Indexed keywords

1 METHYLADENINE; CALCIUM ION; INOSITOL 1,4,5 TRISPHOSPHATE;

ANIMAL CELL; ARTICLE; ASTERIAS; CALCIUM MOBILIZATION; CELL GRANULE; CONTROLLED STUDY; CYTOSKELETON; FERTILIZATION; INTRACELLULAR TRANSPORT; MEIOSIS; NONHUMAN; OOCYTE MATURATION; PRIORITY JOURNAL;

ANIMALIA; ASTERIAS; ASTEROIDEA;

EID: 0033134181     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.1999.4425     Document Type: Article

References (64)

1. Kanatani H., Shirai H., Nakanishi K., Kurosawa T. Isolation and identification of meiosis inducing substance in starfishAsterina amurensis. Nature. 221:1969;273-274.
2. Shen S., Steinhardt R. A. An electrophysiological study of the membrane properties of the immature and mature oocyte of the batstar,Patiria Miniata. Dev. Biol. 48:1976;148-162.
3. Longo F. J. Insemination of immature (Arbacia punctulata. Dev. Biol. 62:1978;271-279.
4. Miyazaki S., Hirai S. Fast polyspermy block and activation potential: Correlated changes during oocyte maturation of a starfish. Dev. Biol. 70:1979;327-340.
5. Hirai S., Nagahama Y., Kishimoto T., Kanatani H. Cytoplasmic maturity revealed by the structural changes in incorporated spermatozoon during the course of starfish oocyte maturation. Dev. Growth Differ. 23:1981;465-478.
6. Dale B., Santella L. Sperm-oocyte interaction in the sea-urchin. J. Cell Sci. 74:1985;153-167.
7. Simoncini L., Moody W. J. Changes in voltage-dependent currents and membrane area during maturation of starfish oocytes: Species differences and similarities. Dev. Biol. 138:1990;194-201.
8. Chambers R. The manner of sperm entry in the starfish egg. Biol. Bull. 58:1930;344-369.
9. Stevens M. Procedures for induction of spawning and meiotic maturation of starfish oocytes by treatment with 1-methyladenine. Exp. Cell Res. 59:1970;482-484.
10. Jaffe L. A., Terasaki M. Structural changes in the endoplasmic reticulum of starfish oocyte during meiotic maturation and fertilization. Dev. Biol. 164:1994;579-587.
11. Longo F. J., So F., Schuetz A. W. Meiotic maturation and the cortical granule reaction in starfish eggs. Biol. Bull. 163:1982;453-476.
12. Longo F. J., Woerner M., Chiba K., Hoshi M. Cortical changes in starfish (Asterina pectinifera. Zygote. 3:1995;225-239.
13. Anderson E. Oocyte differentation in the sea urchin,Arbacia punctulata, J. Cell Biol. 37:1968;514-539.
14. Ducibella T., Duffy P., Buetow J. Quantification and localization of cortical granules during oogenesis in the mouse. Biol. Reprod. 50:1994;467-473.
15. Laidlaw M., Wessel G. M. Cortical granules biogenesis is active throughout oogenesis in sea urchins. Development. 120:1994;1325-1333.
16. Kim N. H., Day B. N., Lee H. T., Chung K. S. Microfilament assembly and cortical granule distribution during maturation, parthenogenetic activation and fertilization in the porcine oocyte. Zygote. 4:1996;145-149.
17. Berg L. K., Wessel G. M. Cortical granules of the sea urchin translocate early in oocyte maturation. Development. 124:1997;1845-1850.
18. Shoj Y., Hamaguchi M. S., Hiramoto Y. Mechanical properties of the endoplasm in starfish oocytes. Exp. Cell Res. 117:1978;79-87.
19. Nemoto S. I., Yoneda M., Uemura I. Marked decrease in the rigidity of starfish oocytes induced by 1-methyladenine. Dev. Growth Differ. 22:1980;315-325.
20. Stricker S. A., Schatten G. The cytoskeleton and nuclear disassembly during germinal vesicle breakdown in starfish oocytes. Dev. Growth Differ. 33:1991;163-171.
21. Heil-Chapdelaine R. A., Otto J. J. Characterization of changes in F-actin during maturation of starfish oocytes. Dev. Biol. 177:1996;204-216.
22. Mazia D. The release of calcium inArbacia. J. Cell Comp. Physiol. 10:1937;291-304.
23. Schuel H. Functions of egg cortical granules. Biology of Fertilization. 1985;Academic Press, New York.
24. Chiba K., Kado R. T., Jaffe L. A. Development of calcium release mechanism during starfish oocyte maturation. Dev. Biol. 140:1990;300-306.
25. Vacquier V. D. The isolation of intact cortical granules from sea urchin eggs: Calcium ions trigger granule discharge. Dev. Biol. 43:1975a;62-74.
26. Jaffe L. F. The role of calcium explosion, waves, and pulse in activating eggs. Metz C. B., Monroy A. Biology of Fertilization. 1985;Academic Press, New York.
27. Bi G.-Q., Alderton J. M., Steinhardt R. A. Calcium-regulated exocytosis is required for cell membrane resealing. J. Cell Biol. 131:1995;1747-1758.
28. Matese J. C., McClay D. R. Cortical granule exocytosis is triggered by different threshold of calcium during fertilisation in sea urchin eggs. Zygote. 6:1998;55-63.
29. Schuel H. Secretory function of egg cortical granules in fertilization and development: A critical review. Gamete Res. 1:1978;299-382.
30. 3. Cell. 73:1993;555-570.
31. McPherson S. M., McPherson P. S., Mathews L., Campbell K. P., Longo F. J. Cortical localization of a calcium release channel in sea urchin eggs. J. Cell Biol. 116:1992;1111-1121.
32. 2+. Nature. 272:1978;251-253.
33. 2+. Biochem. Biophys. Res. Commun. 203:1994;674-680.
34. Santella L. The cell nucleus: An eldorado to future calcium research? J. Membr. Biol. 153:1996;83-94.
35. Santella L. The role of calcium in the cell cycle: Facts and hypotheses. Biochem. Biophys. Res. Commun. 244:1998;317-324.
36. 2+. Cell Calcium. 22:1997;11-20.
37. Stricker S. A., Centonze V. E., Melendez R. F. Calcium dynamics during starfish oocyte maturation and fertilization. Dev. Biol. 165:1994;34-58.
38. Stricker S. A. Time-lapse confocal imaging of calcium dynamics in starfish embryos. Dev. Biol. 170:1995;496-518.
39. Rakow T. L., Shen S. S. Multiple stores of calcium are released in the sea urchin egg during fertilization. Proc. Natl. Acad. Sci. USA. 87:1990;9285-9289.
40. Galione A., McDougall A., Busa W. B., Wilmott N., Gillot I., Withaker M. Redundant mechanisms of calcium-induced calcium release underlying calcium waves during fertilization of sea urchin eggs. Science. 261:1993;348-352.
41. Lee H. C., Aarhus R., Walseth T. F. Calcium mobilization by dual receptors during fertilization of sea urchin eggs. Science. 261:1993;352-355.
42. 2+2+. J. Biol. Chem. 268:1993;7290-7297.
43. Sawada T., Schatten G. Effects of cytoskeleton inhibitors on ooplasma segregation and microtubule organization during fertilization and early development in the ascidianMolgula occidentalis. Dev. Biol. 132:1989;331-342.
44. 2+2+. Dev. Biol. 172:1995;139-157.
45. Schroeder T. E., Stricker S. A. Morphological changes during maturation of starfish oocytes: Surface ultrastructure and cortical actin. Dev. Biol. 98:1983;373-384.
46. Schroeder T. E., Otto J. J. Snoods: A periodic network containing cytokeratin in the cortex of starfish oocytes. Dev. Biol. 144:1991;240-247.
47. Stricker S., Schatten G. The cytoskeleton and nuclear disassembly during germinal vesicle breakdown in starfish oocytes. Dev. Growth Differ. 33:1991;163-171.
48. Crossley I., Whalley T., Whitaker M. Guanosine 5′-thiotriphosphate may stimulate phosphoinositide messenger production in sea urchin eggs by a different route than the fertilizing sperm. Cell Regul. 2:1991;121-133.
49. Whalley T., McDougall A., Crossley I., Swann K., Whitaker M. Internal calcium release and activation of sea urchin eggs by cGMP are independent of the phosphoinositide signaling pathway. Mol. Biol. Cell. 3:1992;373-383.
50. Carroll D. J., Ramarao C. S., Mehlmann L. M., Roche S., Terasaki M. Calcium release at fertilization in starfish eggs is mediated by phospholipase Cγ J. Cell Biol. 138:1997;1303-1311.
51. Berl S., Puszkin S., Nicklas W. J. Acto-myosin-like protein in brain. Science. 179:1973;441-446.
52. De Lorenzo R. J. The calmodulin hypothesis of neurotransmission. Cell Calcium. 2:1981;365-385.
53. Steinhardt R. A., Alderton J. M. Calmodulin confers calcium sensitivity on secretory exocytosis. Nature. 295:1982;154-155.
54. DiMaggio A. J., Lonergan T. A., Stewart-Savage J. Cortical granule exocytosis in hamster eggs requires microfilaments. Mol. Reprod. Dev. 47:1997;334-340.
55. Turner P. R., Sheetz M. P., Jaffe L. A. Fertlization increases the polyphosphoinisitide content of sea urchin eggs. Nature. 332:1984;414-415.
56. Ciapa B., Whitaker M. J. Two phases of inositol polyphosphate and diacylglycerol production at fertilisation. FEBS Lett. 195:1986;347-351.
57. Ciapa B., Pesando D., Wilding M., Whitaker M. Cell-cycle calcium transient driven by cyclic changes in inosotol trisphosphate levels. Nature. 368:1994;875-878.
58. Lee S. J., Shen S. S. The calcium transient in sea urchin eggs during fertilization requires the production of inositol 1,4,5-trisphosphate. Dev. Biol. 193:1998;195-208.
59. Grey R. D., Wolf D. P., Hedrick J. L. Formation and structure of the fertilization envelope inXenopus laevis. Dev. Biol. 36:1974;44-61.
60. Campanella C., Andreuccetti P., Taddei C., Talevi R. The modification of cortical endoplasmic reticulum duringin vitroXenopus laevis. J. Exp. Zool. 229:1984;283-293.
61. Larabell C. A., Chandler D. E. Freeze-fracture analysis of structural reorganization during meiotic maturation in oocytes ofXenopus laevis. Cell Tissue Res. 251:1988;129-136.
62. Witchel H. J., Steinhardt R. A. 1-Methyladenine can consistently induce a fura-detectable transient calcium increase which is neither necessary nor sufficient for maturation in oocytes of the starfishAsterina miniata. Dev. Biol. 141:1990;393-398.
63. Kikuyama M., Hiramoto Y. Change in intracellular calcium ions upon maturation in starfish oocytes. Dev. Growth Differ. 33:1991;633-638.
64. Whitaker M., Baker P. F. Calcium-dependent exocytosis in anin vitro. Proc. R. Soc. Lond. B. 218:1983;397-413.