Abstract
The calcium indicator dye fluo-3/AM was loaded into the ER of isolated cortices of unfertilized eggs of the sea urchin Arbacia punctulata. Development of the fluorescent signal took from 8 to 40 min and usually required 1 mM ATP. The signal decreased to a minimum level within 30 s after perfusion with 1 microM InsP3 and increased within 5 min when InsP3 was replaced with 1 mM ATP. Also, the fluorescence signal was lowered rapidly by perfusion with 10 microM A23187 or 10 microM ionomycin. These findings demonstrate that the cortical ER is a site of ATP-dependent calcium sequestration and InsP3-induced calcium release. A light-induced wave of calcium release, traveling between 0.7 and 2.8 microns/s (average speed 1.4 microns/s, N = 8), was sometimes observed during time lapse recordings; it may therefore be possible to use the isolated cortex preparation to investigate the postfertilization calcium wave.
Full Text
The Full Text of this article is available as a PDF (908.7 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Brady S. T., Lasek R. J., Allen R. D., Yin H. L., Stossel T. P. Gelsolin inhibition of fast axonal transport indicates a requirement for actin microfilaments. Nature. 1984 Jul 5;310(5972):56–58. doi: 10.1038/310056a0. [DOI] [PubMed] [Google Scholar]
- Chandler D. E. Exocytosis in vitro: ultrastructure of the isolated sea urchin egg cortex as seen in platinum replicas. J Ultrastruct Res. 1984 Nov;89(2):198–211. doi: 10.1016/s0022-5320(84)80015-5. [DOI] [PubMed] [Google Scholar]
- Clapper D. L., Lee H. C. Inositol trisphosphate induces calcium release from nonmitochondrial stores i sea urchin egg homogenates. J Biol Chem. 1985 Nov 15;260(26):13947–13954. [PubMed] [Google Scholar]
- Detering N. K., Decker G. L., Schmell E. D., Lennarz W. J. Isolation and characterization of plasma membrane-associated cortical granules from sea urchin eggs. J Cell Biol. 1977 Dec;75(3):899–914. doi: 10.1083/jcb.75.3.899. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisen A., Kiehart D. P., Wieland S. J., Reynolds G. T. Temporal sequence and spatial distribution of early events of fertilization in single sea urchin eggs. J Cell Biol. 1984 Nov;99(5):1647–1654. doi: 10.1083/jcb.99.5.1647. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ferris C. D., Huganir R. L., Snyder S. H. Calcium flux mediated by purified inositol 1,4,5-trisphosphate receptor in reconstituted lipid vesicles is allosterically regulated by adenine nucleotides. Proc Natl Acad Sci U S A. 1990 Mar;87(6):2147–2151. doi: 10.1073/pnas.87.6.2147. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 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]
- Gillot I., Payan P., Girard J. P., Sardet C. Calcium in sea urchin egg during fertilization. Int J Dev Biol. 1990 Mar;34(1):117–125. [PubMed] [Google Scholar]
- Hafner M., Petzelt C., Nobiling R., Pawley J. B., Kramp D., Schatten G. Wave of free calcium at fertilization in the sea urchin egg visualized with fura-2. Cell Motil Cytoskeleton. 1988;9(3):271–277. doi: 10.1002/cm.970090309. [DOI] [PubMed] [Google Scholar]
- Hamaguchi Y., Hamaguchi M. S. Simultaneous investigation of intracellular Ca2+ increase and morphological events upon fertilization in the sand dollar egg. Cell Struct Funct. 1990 Jun;15(3):159–162. doi: 10.1247/csf.15.159. [DOI] [PubMed] [Google Scholar]
- Hamaguchi Y., Hiramoto Y. Activation of sea urchin eggs by microinjection of calcium buffers. Exp Cell Res. 1981 Jul;134(1):171–179. doi: 10.1016/0014-4827(81)90474-2. [DOI] [PubMed] [Google Scholar]
- Hashimoto S., Bruno B., Lew D. P., Pozzan T., Volpe P., Meldolesi J. Immunocytochemistry of calciosomes in liver and pancreas. J Cell Biol. 1988 Dec;107(6 Pt 2):2523–2531. doi: 10.1083/jcb.107.6.2523. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Henson J. H., Begg D. A., Beaulieu S. M., Fishkind D. J., Bonder E. M., Terasaki M., Lebeche D., Kaminer B. A calsequestrin-like protein in the endoplasmic reticulum of the sea urchin: localization and dynamics in the egg and first cell cycle embryo. J Cell Biol. 1989 Jul;109(1):149–161. doi: 10.1083/jcb.109.1.149. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jaffe L. F. Sources of calcium in egg activation: a review and hypothesis. Dev Biol. 1983 Oct;99(2):265–276. doi: 10.1016/0012-1606(83)90276-2. [DOI] [PubMed] [Google Scholar]
- Mignery G. A., Südhof T. C., Takei K., De Camilli P. Putative receptor for inositol 1,4,5-trisphosphate similar to ryanodine receptor. Nature. 1989 Nov 9;342(6246):192–195. doi: 10.1038/342192a0. [DOI] [PubMed] [Google Scholar]
- Minta A., Kao J. P., Tsien R. Y. Fluorescent indicators for cytosolic calcium based on rhodamine and fluorescein chromophores. J Biol Chem. 1989 May 15;264(14):8171–8178. [PubMed] [Google Scholar]
- Oberdorf J. A., Head J. F., Kaminer B. Calcium uptake and release by isolated cortices and microsomes from the unfertilized egg of the sea urchin Strongylocentrotus droebachiensis. J Cell Biol. 1986 Jun;102(6):2205–2210. doi: 10.1083/jcb.102.6.2205. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Oberdorf J. A., Lebeche D., Head J. F., Kaminer B. Identification of a calsequestrin-like protein from sea urchin eggs. J Biol Chem. 1988 May 15;263(14):6806–6809. [PubMed] [Google Scholar]
- Otsu H., Yamamoto A., Maeda N., Mikoshiba K., Tashiro Y. Immunogold localization of inositol 1, 4, 5-trisphosphate (InsP3) receptor in mouse cerebellar Purkinje cells using three monoclonal antibodies. Cell Struct Funct. 1990 Jun;15(3):163–173. doi: 10.1247/csf.15.163. [DOI] [PubMed] [Google Scholar]
- Payan P., Girard J. P., Sardet C., Whitaker M., Zimmerberg J. Uptake and release of calcium by isolated egg cortices of the sea urchin Paracentrotus lividus. Biol Cell. 1986;58(1):87–90. doi: 10.1111/j.1768-322x.1986.tb00490.x. [DOI] [PubMed] [Google Scholar]
- Ross C. A., Meldolesi J., Milner T. A., Satoh T., Supattapone S., Snyder S. H. Inositol 1,4,5-trisphosphate receptor localized to endoplasmic reticulum in cerebellar Purkinje neurons. Nature. 1989 Jun 8;339(6224):468–470. doi: 10.1038/339468a0. [DOI] [PubMed] [Google Scholar]
- Sardet C. The ultrastructure of the sea urchin egg cortex isolated before and after fertilization. Dev Biol. 1984 Sep;105(1):196–210. doi: 10.1016/0012-1606(84)90275-6. [DOI] [PubMed] [Google Scholar]
- Satoh T., Ross C. A., Villa A., Supattapone S., Pozzan T., Snyder S. H., Meldolesi J. The inositol 1,4,5,-trisphosphate receptor in cerebellar Purkinje cells: quantitative immunogold labeling reveals concentration in an ER subcompartment. J Cell Biol. 1990 Aug;111(2):615–624. doi: 10.1083/jcb.111.2.615. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Supattapone S., Danoff S. K., Theibert A., Joseph S. K., Steiner J., Snyder S. H. Cyclic AMP-dependent phosphorylation of a brain inositol trisphosphate receptor decreases its release of calcium. Proc Natl Acad Sci U S A. 1988 Nov;85(22):8747–8750. doi: 10.1073/pnas.85.22.8747. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Terasaki M., Jaffe L. A. Organization of the sea urchin egg endoplasmic reticulum and its reorganization at fertilization. J Cell Biol. 1991 Sep;114(5):929–940. doi: 10.1083/jcb.114.5.929. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vacquier V. D. The isolation of intact cortical granules from sea urchin eggs: calcium lons trigger granule discharge. Dev Biol. 1975 Mar;43(1):62–74. doi: 10.1016/0012-1606(75)90131-1. [DOI] [PubMed] [Google Scholar]
- Volpe P., Krause K. H., Hashimoto S., Zorzato F., Pozzan T., Meldolesi J., Lew D. P. "Calciosome," a cytoplasmic organelle: the inositol 1,4,5-trisphosphate-sensitive Ca2+ store of nonmuscle cells? Proc Natl Acad Sci U S A. 1988 Feb;85(4):1091–1095. doi: 10.1073/pnas.85.4.1091. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Whitaker M. J., Steinhardt R. A. Ionic regulation of egg activation. Q Rev Biophys. 1982 Nov;15(4):593–666. doi: 10.1017/s0033583500003760. [DOI] [PubMed] [Google Scholar]