Abstract
Unfertilized eggs of the medaka fish (Oryzias latipes) were injected with pH-buffered calcium buffers. Medaka egg activation is accompanied by a transient increase in cytoplasmic free calcium (Gilkey, J. C., L. F. Jaffe, E. B. Ridgway, and G. T. Reynolds, 1978, J. Cell Biol., 76:448-466). The calcium buffer injections demonstrated that (a) the threshold free calcium required to elicit the calcium transient and activate the egg is between 1.7 and 5.1 microM at pH 7.0, well below the 30 microM reached during the transient, and (b) buffers which hold free calcium below threshold prevent activation of the buffered region in subsequently fertilized eggs. Therefore an increase in free calcium is necessary and sufficient to elicit the calcium transient, and the calcium transient is necessary to activate the egg. Further, these results are additional proof that the calcium transient is initiated and propagated through the cytoplasm by a mechanism of calcium- stimulated calcium release. Finally, a normal calcium transient must propagate through the entire cytoplasm to ensure normal development. Unfertilized eggs were injected with pH buffers to produce short-term, localized changes in cytoplasmic pH. The eggs were then fertilized at various times after injection. In other experiments, unfertilized and fertilized eggs were exposed to media containing either NH4Cl or CO2 to produce longer term, global changes in cytoplasmic pH. These treatments neither activated the eggs nor interfered with the normal development of fertilized eggs, suggesting that even if a natural change in cytoplasmic pH is induced by activation, it has no role in medaka egg development. The injected pH buffers altered the rate of propagation of the calcium transient through the cytoplasm, suggesting that the threshold free calcium required to trigger calcium-stimulated calcium release might be pH dependent. The results of injection of pH-buffered calcium buffers support this conjecture: for a tenfold increase in hydrogen ion concentration, free calcium must also be raised tenfold to elicit the calcium transient.
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- Baker P. F., Whitaker M. J. Influence of ATP and calcium on the cortical reaction in sea urchin eggs. Nature. 1978 Nov 30;276(5687):513–515. doi: 10.1038/276513a0. [DOI] [PubMed] [Google Scholar]
- Chambers E. L., Hinkley R. E. Non-propagated cortical reactions induced by the divalent ionophore A23187 in eggs of the sea urchin, Lytechinus variegatus. Exp Cell Res. 1979 Dec;124(2):441–446. doi: 10.1016/0014-4827(79)90221-0. [DOI] [PubMed] [Google Scholar]
- Crawford R. B., Wilde C. E., Jr, Heinemann M. H., Hendler F. J. Morphogenetic disturbances from timed inhibitions of protein synthesis in fundulus. J Embryol Exp Morphol. 1973 Apr;29(2):363–382. [PubMed] [Google Scholar]
- Cross N. L. Initiation of the activation potential by an increase in intracellular calcium in eggs of the frog, Rana pipiens. Dev Biol. 1981 Jul 30;85(2):380–384. doi: 10.1016/0012-1606(81)90269-4. [DOI] [PubMed] [Google Scholar]
- Cuthbertson K. S., Whittingham D. G., Cobbold P. H. Free Ca2+ increases in exponential phases during mouse oocyte activation. Nature. 1981 Dec 24;294(5843):754–757. doi: 10.1038/294754a0. [DOI] [PubMed] [Google Scholar]
- Dipolo R., Beaugé L. The effect of pH on Ca2+ extrusion mechanisms in dialyzed squid axons. Biochim Biophys Acta. 1982 May 21;688(1):237–245. doi: 10.1016/0005-2736(82)90599-5. [DOI] [PubMed] [Google Scholar]
- Epel D. Ionic triggers in the fertilization of sea urchin eggs. Ann N Y Acad Sci. 1980;339:74–85. doi: 10.1111/j.1749-6632.1980.tb15970.x. [DOI] [PubMed] [Google Scholar]
- Epel D. Mechanisms of activation of sperm and egg during fertilization of sea urchin gametes. Curr Top Dev Biol. 1978;12:185–246. doi: 10.1016/s0070-2153(08)60597-9. [DOI] [PubMed] [Google Scholar]
- Fabiato A., Fabiato F. Effects of pH on the myofilaments and the sarcoplasmic reticulum of skinned cells from cardiace and skeletal muscles. J Physiol. 1978 Mar;276:233–255. doi: 10.1113/jphysiol.1978.sp012231. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Flatman P., Lew V. L. Use of ionophore A23187 to measure and to control free and bound cytoplasmic Mg in intact red cells. Nature. 1977 May 26;267(5609):360–362. doi: 10.1038/267360a0. [DOI] [PubMed] [Google Scholar]
- Fulton B. P., Whittingham D. G. Activation of mammalian oocytes by intracellular injection of calcium. Nature. 1978 May 11;273(5658):149–151. doi: 10.1038/273149a0. [DOI] [PubMed] [Google Scholar]
- Gardiner D. M., Grey R. D. Membrane junctions in Xenopus eggs: their distribution suggests a role in calcium regulation. J Cell Biol. 1983 Apr;96(4):1159–1163. doi: 10.1083/jcb.96.4.1159. [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]
- Godt R. E. A simple electrostatic model can explain the effect of pH upon the force-pCa relation of skinned frog skeletal muscle fibers. Biophys J. 1981 Aug;35(2):385–392. doi: 10.1016/S0006-3495(81)84797-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Grainger J. L., Winkler M. M., Shen S. S., Steinhardt R. A. Intracellular pH controls protein synthesis rate in the sea urchine egg and early embryo. Dev Biol. 1979 Feb;68(2):396–406. doi: 10.1016/0012-1606(79)90213-6. [DOI] [PubMed] [Google Scholar]
- Gupta R. K., Yushok W. D. Noninvasive 31P NMR probes of free Mg2+, MgATP, and MgADP in intact Ehrlich ascites tumor cells. Proc Natl Acad Sci U S A. 1980 May;77(5):2487–2491. doi: 10.1073/pnas.77.5.2487. [DOI] [PMC free article] [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]
- Hollinger T. G., Schuetz A. W. "Cleavage" and cortical granule breakdown in Rana pipiens oocytes induced by direct microinjection of calcium. J Cell Biol. 1976 Nov;71(2):395–401. doi: 10.1083/jcb.71.2.395. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Jaffe L. F. Calcium explosions as triggers of development. Ann N Y Acad Sci. 1980;339:86–101. doi: 10.1111/j.1749-6632.1980.tb15971.x. [DOI] [PubMed] [Google Scholar]
- Johnson C. H., Epel D. Intracellular pH of sea urchin eggs measured by the dimethyloxazolidinedione (DMO) method. J Cell Biol. 1981 May;89(2):284–291. doi: 10.1083/jcb.89.2.284. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson C. H., Epel D. Starfish oocyte maturation and fertilization: intracellular pH is not involved in activation. Dev Biol. 1982 Aug;92(2):461–469. doi: 10.1016/0012-1606(82)90191-9. [DOI] [PubMed] [Google Scholar]
- Johnson J. D., Epel D. Intracellular pH and activation of sea urchin eggs after fertilisation. Nature. 1976 Aug 19;262(5570):661–664. doi: 10.1038/262661a0. [DOI] [PubMed] [Google Scholar]
- Lea T. J., Ashley C. C. Carbon dioxide or bicarbonate ions release Ca2+ from internal stores in crustacean myofibrillar bundles. J Membr Biol. 1981;61(2):115–125. doi: 10.1007/BF02007638. [DOI] [PubMed] [Google Scholar]
- Lopo A., Vacquier V. D. The rise and fall of intracellular pH of sea urchin eggs after fertilisation. Nature. 1977 Oct 13;269(5629):590–592. doi: 10.1038/269590a0. [DOI] [PubMed] [Google Scholar]
- Nuccitelli R., Webb D. J., Lagier S. T., Matson G. B. 31P NMR reveals increased intracellular pH after fertilization in Xenopus eggs. Proc Natl Acad Sci U S A. 1981 Jul;78(7):4421–4425. doi: 10.1073/pnas.78.7.4421. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ridgway E. B., Gilkey J. C., Jaffe L. F. Free calcium increases explosively in activating medaka eggs. Proc Natl Acad Sci U S A. 1977 Feb;74(2):623–627. doi: 10.1073/pnas.74.2.623. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rink T. J., Tsien R. Y., Pozzan T. Cytoplasmic pH and free Mg2+ in lymphocytes. J Cell Biol. 1982 Oct;95(1):189–196. doi: 10.1083/jcb.95.1.189. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rink T. J., Tsien R. Y., Warner A. E. Free calcium in Xenopus embryos measured with ion-selective microelectrodes. Nature. 1980 Feb 14;283(5748):658–660. doi: 10.1038/283658a0. [DOI] [PubMed] [Google Scholar]
- Roos A., Boron W. F. Intracellular pH. Physiol Rev. 1981 Apr;61(2):296–434. doi: 10.1152/physrev.1981.61.2.296. [DOI] [PubMed] [Google Scholar]
- Rose B., Rick R. Intracellular pH, intracellular free Ca, and junctional cell-cell coupling. J Membr Biol. 1978 Dec 29;44(3-4):377–415. doi: 10.1007/BF01944230. [DOI] [PubMed] [Google Scholar]
- Shen S. S., Steinhardt R. A. Direct measurement of intracellular pH during metabolic derepression of the sea urchin egg. Nature. 1978 Mar 16;272(5650):253–254. doi: 10.1038/272253a0. [DOI] [PubMed] [Google Scholar]
- Shen S. S. The effect of external ions on pHi in sea urchin eggs. Kroc Found Ser. 1981;15:269–282. [PubMed] [Google Scholar]
- Steinhardt R., Zucker R., Schatten G. Intracellular calcium release at fertilization in the sea urchin egg. Dev Biol. 1977 Jul 1;58(1):185–196. doi: 10.1016/0012-1606(77)90084-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walz B. Ca2+-sequestering smooth endoplasmic reticulum in an invertebrate photoreceptor. I. Intracellular topography as revealed by OsFeCN staining and in situ Ca accumulation. J Cell Biol. 1982 Jun;93(3):839–848. doi: 10.1083/jcb.93.3.839. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Walz B. Ca2+-sequestering smooth endoplasmic reticulum in an invertebrate photoreceptor. II. Its properties as revealed by microphotometric measurements. J Cell Biol. 1982 Jun;93(3):849–859. doi: 10.1083/jcb.93.3.849. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wasserman W. J., Pinto L. H., O'Connor C. M., Smith L. D. Progesterone induces a rapid increase in [Ca2+]in of Xenopus laevis oocytes. Proc Natl Acad Sci U S A. 1980 Mar;77(3):1534–1536. doi: 10.1073/pnas.77.3.1534. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Webb D. J., Nuccitelli R. Direct measurement of intracellular pH changes in Xenopus eggs at fertilization and cleavage. J Cell Biol. 1981 Nov;91(2 Pt 1):562–567. doi: 10.1083/jcb.91.2.562. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Webb D. J., Nuccitelli R. Intracellular pH changes accompanying the activation of development in frog eggs: comparison of pH microelectrodes and 31P-NMR measurements. Kroc Found Ser. 1981;15:293–324. [PubMed] [Google Scholar]
- Wilde C. E., Jr, Crawford R. B. Cellular differentiation in the anamniota. 3. Effects of actinomycin D and cyanide on the morphogenesis of Fundulus. Exp Cell Res. 1966 Nov-Dec;44(2):471–488. doi: 10.1016/0014-4827(66)90453-8. [DOI] [PubMed] [Google Scholar]
- Winkler M. M., Matson G. B., Hershey J. W., Bradbury E. M. 31P-NMR study of the activation of the sea urchin egg. Exp Cell Res. 1982 May;139(1):217–222. doi: 10.1016/0014-4827(82)90335-4. [DOI] [PubMed] [Google Scholar]
- Winkler M. M., Steinhardt R. A., Grainger J. L., Minning L. Dual ionic controls for the activation of protein synthesis at fertilization. Nature. 1980 Oct 9;287(5782):558–560. doi: 10.1038/287558a0. [DOI] [PubMed] [Google Scholar]
- YAMAMOTO T. O. Physiology of fertilization in fish eggs. Int Rev Cytol. 1961;12:361–405. doi: 10.1016/s0074-7696(08)60545-8. [DOI] [PubMed] [Google Scholar]
- Zucker R. S., Steinhardt R. A. Prevention of the cortical reaction in fertilized sea urchin eggs by injection of calcium-chelating ligands. Biochim Biophys Acta. 1978 Jul 17;541(4):459–466. doi: 10.1016/0304-4165(78)90155-1. [DOI] [PubMed] [Google Scholar]