Skip to main content
The Journal of Cell Biology logoLink to The Journal of Cell Biology
. 1995 Nov 2;131(4):963–973. doi: 10.1083/jcb.131.4.963

Regulatory mechanisms of the acrosome reaction revealed by multiview microscopy of single starfish sperm

PMCID: PMC2199994  PMID: 7490297

Abstract

The acrosome reaction in many animals is a coupled reaction involving an exocytotic step and a dramatic change in cell shape. It has been proposed that these morphological changes are regulated by intracellular ions such as Ca2+ and H+. We report here simultaneous visualization, under a multiview microscope, of intracellular free Ca2+ concentration ([Ca2+]i), intracellular pH (pHi), and morphological changes in a single starfish sperm (Asterina pectinifera). [Ca2+]i and pHi were monitored with the fluorescent probes indo-1 and SNARF-1, respectively. The acrosome reaction was induced with ionomycin. After the introduction of ionomycin in the medium, [Ca2+]i increased gradually and reached a plateau in approximately 30 s. The fusion of the acrosomal vacuole took place abruptly before the plateau, during the rising phase. Although the speed of the [Ca2+]i increase varied among the many sperm tested, exocytosis in all cases occurred at the same [Ca2+]i of approximately 2 microM (estimated using the dissociation constant of indo-1 for Ca2+ of 1.1 microM). This result suggests that the exocytotic mechanism in starfish sperm responds to [Ca2+]i rapidly, with a reaction time of the order of one second or less. Unlike the change in [Ca2+]i, an abrupt increase in pHi was observed immediately after exocytosis, suggesting the presence of a proton mobilizing system that is triggered by exocytosis. The rapid increase in pHi coincided with the formation of the acrosomal rod and the beginning of vigorous movement of the flagellum, both of which have been proposed to be pHi dependent. The exocytotic event itself was visualized with the fluorescent membrane probe RH292. The membrane of the acrosomal vacuole, concealed from the external medium in an unreacted sperm, was seen to fuse with the plasma membrane.

Full Text

The Full Text of this article is available as a PDF (3.8 MB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Castellano L. E., López-Godínez J., Aldana G., Barrios-Rodiles M., Obregón A., García de De la Torre L., Darszon A., García-Soto J. The acrosome reaction in digitonin-permeabilized sea urchin sperm in the absence of the natural inducer. Eur J Cell Biol. 1995 May;67(1):23–31. [PubMed] [Google Scholar]
  2. Christen R., Schackmann R. W., Shapiro B. M. Elevation of the intracellular pH activates respiration and motility of sperm of the sea urchin, Strongylocentrotus purpuratus. J Biol Chem. 1982 Dec 25;257(24):14881–14890. [PubMed] [Google Scholar]
  3. Christen R., Schackmann R. W., Shapiro B. M. Metabolism of sea urchin sperm. Interrelationships between intracellular pH, ATPase activity, and mitochondrial respiration. J Biol Chem. 1983 May 10;258(9):5392–5399. [PubMed] [Google Scholar]
  4. Collins F., Epel D. The role of calcium ions in the acrosome reaction of sea urchin sperm: regulation of exocytosis. Exp Cell Res. 1977 Apr;106(1):211–222. doi: 10.1016/0014-4827(77)90258-0. [DOI] [PubMed] [Google Scholar]
  5. Creutz C. E. The annexins and exocytosis. Science. 1992 Nov 6;258(5084):924–931. doi: 10.1126/science.1439804. [DOI] [PubMed] [Google Scholar]
  6. Dan J. C., Hagiwara Y. Studies on the acrosome. IX. Course of acrosome reaction in the starfish. J Ultrastruct Res. 1967 Jun;18(5):562–579. doi: 10.1016/s0022-5320(67)80203-x. [DOI] [PubMed] [Google Scholar]
  7. DeBello W. M., Betz H., Augustine G. J. Synaptotagmin and neurotransmitter release. Cell. 1993 Sep 24;74(6):947–950. doi: 10.1016/0092-8674(93)90716-4. [DOI] [PubMed] [Google Scholar]
  8. Dunn K. W., Mayor S., Myers J. N., Maxfield F. R. Applications of ratio fluorescence microscopy in the study of cell physiology. FASEB J. 1994 Jun;8(9):573–582. doi: 10.1096/fasebj.8.9.8005385. [DOI] [PubMed] [Google Scholar]
  9. Feigenson G. W. Calcium ion binding between lipid bilayers: the four-component system of phosphatidylserine, phosphatidylcholine, calcium chloride, and water. Biochemistry. 1989 Feb 7;28(3):1270–1278. doi: 10.1021/bi00429a048. [DOI] [PubMed] [Google Scholar]
  10. Feigenson G. W. On the nature of calcium ion binding between phosphatidylserine lamellae. Biochemistry. 1986 Sep 23;25(19):5819–5825. doi: 10.1021/bi00367a071. [DOI] [PubMed] [Google Scholar]
  11. Ferro-Novick S., Jahn R. Vesicle fusion from yeast to man. Nature. 1994 Jul 21;370(6486):191–193. doi: 10.1038/370191a0. [DOI] [PubMed] [Google Scholar]
  12. Florman H. M. Sequential focal and global elevations of sperm intracellular Ca2+ are initiated by the zona pellucida during acrosomal exocytosis. Dev Biol. 1994 Sep;165(1):152–164. doi: 10.1006/dbio.1994.1242. [DOI] [PubMed] [Google Scholar]
  13. Florman H. M., Tombes R. M., First N. L., Babcock D. F. An adhesion-associated agonist from the zona pellucida activates G protein-promoted elevations of internal Ca2+ and pH that mediate mammalian sperm acrosomal exocytosis. Dev Biol. 1989 Sep;135(1):133–146. doi: 10.1016/0012-1606(89)90164-4. [DOI] [PubMed] [Google Scholar]
  14. Garbers D. L. Molecular basis of fertilization. Annu Rev Biochem. 1989;58:719–742. doi: 10.1146/annurev.bi.58.070189.003443. [DOI] [PubMed] [Google Scholar]
  15. González-Martínez M. T., Guerrero A., Morales E., de De La Torre L., Darszon A. A depolarization can trigger Ca2+ uptake and the acrosome reaction when preceded by a hyperpolarization in L. pictus sea urchin sperm. Dev Biol. 1992 Mar;150(1):193–202. doi: 10.1016/0012-1606(92)90018-c. [DOI] [PubMed] [Google Scholar]
  16. Grynkiewicz G., Poenie M., Tsien R. Y. A new generation of Ca2+ indicators with greatly improved fluorescence properties. J Biol Chem. 1985 Mar 25;260(6):3440–3450. [PubMed] [Google Scholar]
  17. Guerrero A., Darszon A. Egg jelly triggers a calcium influx which inactivates and is inhibited by calmodulin antagonists in the sea urchin sperm. Biochim Biophys Acta. 1989 Mar 27;980(1):109–116. doi: 10.1016/0005-2736(89)90206-x. [DOI] [PubMed] [Google Scholar]
  18. Guerrero A., Darszon A. Evidence for the activation of two different Ca2+ channels during the egg jelly-induced acrosome reaction of sea urchin sperm. J Biol Chem. 1989 Nov 25;264(33):19593–19599. [PubMed] [Google Scholar]
  19. Heidelberger R., Heinemann C., Neher E., Matthews G. Calcium dependence of the rate of exocytosis in a synaptic terminal. Nature. 1994 Oct 6;371(6497):513–515. doi: 10.1038/371513a0. [DOI] [PubMed] [Google Scholar]
  20. Hoshi M., Amano T., Okita Y., Okinaga T., Matsui T. Egg signals for triggering the acrosome reaction in starfish spermatozoa. J Reprod Fertil Suppl. 1990;42:23–31. [PubMed] [Google Scholar]
  21. Hoshi M., Matsui T., Nishiyama I., Amano T., Okita Y. Physiological inducers of the acrosome reaction. Cell Differ Dev. 1988 Nov;25 (Suppl):19–24. doi: 10.1016/0922-3371(88)90095-0. [DOI] [PubMed] [Google Scholar]
  22. Hoshi M., Nishigaki T., Ushiyama A., Okinaga T., Chiba K., Matsumoto M. Egg-jelly signal molecules for triggering the acrosome reaction in starfish spermatozoa. Int J Dev Biol. 1994 Jun;38(2):167–174. [PubMed] [Google Scholar]
  23. Kauffman R. F., Taylor R. W., Pfeiffer D. R. Cation transport and specificity of ionomycin. Comparison with ionophore A23187 in rat liver mitochondria. J Biol Chem. 1980 Apr 10;255(7):2735–2739. [PubMed] [Google Scholar]
  24. Kinosita K., Jr, Itoh H., Ishiwata S., Hirano K., Nishizaka T., Hayakawa T. Dual-view microscopy with a single camera: real-time imaging of molecular orientations and calcium. J Cell Biol. 1991 Oct;115(1):67–73. doi: 10.1083/jcb.115.1.67. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Morris S. J. Real-time multi-wavelength fluorescence imaging of living cells. Biotechniques. 1990 Mar;8(3):296–308. [PubMed] [Google Scholar]
  26. Sardet C., Tilney L. G. Origin of the membrane for the acrosomal process: is actin complexed with membrane precursors? Cell Biol Int Rep. 1977 Mar;1(2):193–200. doi: 10.1016/0309-1651(77)90040-6. [DOI] [PubMed] [Google Scholar]
  27. Schackmann R. W., Chock P. B. Alteration of intracellular [Ca2+] in sea urchin sperm by the egg peptide speract. Evidence that increased intracellular Ca2+ is coupled to Na+ entry and increased intracellular pH. J Biol Chem. 1986 Jul 5;261(19):8719–8728. [PubMed] [Google Scholar]
  28. Schackmann R. W., Eddy E. M., Shapiro B. M. The acrosome reaction of Strongylocentrotus purpuratus sperm. Ion requirements and movements. Dev Biol. 1978 Aug;65(2):483–495. doi: 10.1016/0012-1606(78)90043-x. [DOI] [PubMed] [Google Scholar]
  29. Schackmann R. W., Shapiro B. M. A partial sequence of ionic changes associated with the acrosome reaction of Strongylocentrotus purpuratus. Dev Biol. 1981 Jan 15;81(1):145–154. doi: 10.1016/0012-1606(81)90357-2. [DOI] [PubMed] [Google Scholar]
  30. Schroeder T. E., Christen R. Polymerization of actin without acrosomal exocytosis in starfish sperm. Visualization with NBD-phallacidin. Exp Cell Res. 1982 Aug;140(2):363–371. doi: 10.1016/0014-4827(82)90125-2. [DOI] [PubMed] [Google Scholar]
  31. Suzuki K., Tanaka Y., Nakajima Y., Hirano K., Itoh H., Miyata H., Hayakawa T., Kinosita K., Jr Spatiotemporal relationships among early events of fertilization in sea urchin eggs revealed by multiview microscopy. Biophys J. 1995 Mar;68(3):739–748. doi: 10.1016/S0006-3495(95)80289-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
  32. Tilney L. G., Inoué S. Acrosomal reaction of Thyone sperm. II. The kinetics and possible mechanism of acrosomal process elongation. J Cell Biol. 1982 Jun;93(3):820–827. doi: 10.1083/jcb.93.3.820. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. Tilney L. G., Kiehart D. P., Sardet C., Tilney M. Polymerization of actin. IV. Role of Ca++ and H+ in the assembly of actin and in membrane fusion in the acrosomal reaction of echinoderm sperm. J Cell Biol. 1978 May;77(2):536–550. doi: 10.1083/jcb.77.2.536. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Trimmer J. S., Schackmann R. W., Vacquier V. D. Monoclonal antibodies increase intracellular Ca2+ in sea urchin spermatozoa. Proc Natl Acad Sci U S A. 1986 Dec;83(23):9055–9059. doi: 10.1073/pnas.83.23.9055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  35. Vogel S. S., Zimmerberg J. Proteins on exocytic vesicles mediate calcium-triggered fusion. Proc Natl Acad Sci U S A. 1992 May 15;89(10):4749–4753. doi: 10.1073/pnas.89.10.4749. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Watson P. F., Plummer J. M., Jones P. S. The ionophore-induced acrosome reaction differs structurally from the spontaneous acrosome reaction. J Exp Zool. 1992 Nov 1;264(2):231–235. doi: 10.1002/jez.1402640217. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Cell Biology are provided here courtesy of The Rockefeller University Press

RESOURCES