Abstract
Previous work has established that the polyspermy block in Urechis acts at the level of sperm-egg membrane fusion. (J. Exp. Zool. 196:105). Present results indicate that during the first 5--10 min after insemination the block is mediated by a positive shift in membrane potential (the fertilization potential) elicited by the penetrating sperm, since holding the membrane potential of the unfertilized egg positive by passing current reduces the probability of sperm entry, while progressively reducing the amplitude of the fertilization potential by decreasing external Na+ progressively enhances multiple sperm penetrations. Also, a normal fertilization potential is correlated with a polyspermy block even under conditions (pH 7) in which eggs do not develop. We have investigated the mechanism of the electrical polyspermy block by quantifying the relationship between sperm incorporation, membrane potential and ion fluxes. Results indicate that the polyspermy block is mediated by the electrial change per se and not by the associated fluxes of Na+, Ca++, and H+.
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- BRADEN A. W., AUSTIN C. R., DAVID H. A. The reaction of zona pellucida to sperm penetration. Aust J Biol Sci. 1954 Aug;7(3):391–409. doi: 10.1071/bi9540391. [DOI] [PubMed] [Google Scholar]
- Campisi J., Scandella C. J. Fertilization-induced changes in membrane fluidity of sea urchin eggs. Science. 1978 Mar 24;199(4335):1336–1337. doi: 10.1126/science.564549. [DOI] [PubMed] [Google Scholar]
- Cohen L. B., Salzberg B. M. Optical measurement of membrane potential. Rev Physiol Biochem Pharmacol. 1978;83:35–88. doi: 10.1007/3-540-08907-1_2. [DOI] [PubMed] [Google Scholar]
- Ehrenstein G., Lecar H. Electrically gated ionic channels in lipid bilayers. Q Rev Biophys. 1977 Feb;10(1):1–34. doi: 10.1017/s0033583500000123. [DOI] [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]
- Gould-Somero M., Holland L. Fine structural investigation of the insemination response in Urechis caupo. Dev Biol. 1975 Oct;46(2):358–369. doi: 10.1016/0012-1606(75)90112-8. [DOI] [PubMed] [Google Scholar]
- Gould-Somero M., Holland L., Paul M. Cytochalasin B inhibits sperm penetration into eggs of Urechis caupo (Echiura). Dev Biol. 1977 Jul 1;58(1):11–22. doi: 10.1016/0012-1606(77)90071-9. [DOI] [PubMed] [Google Scholar]
- Hagiwara S., Jaffe L. A. Electrical properties of egg cell membranes. Annu Rev Biophys Bioeng. 1979;8:385–416. doi: 10.1146/annurev.bb.08.060179.002125. [DOI] [PubMed] [Google Scholar]
- Holland N. D. The fine structure of Comanthus japonica (Echinodermata: Crinoidea) from zygote through early gastrula. Tissue Cell. 1978;10(1):93–112. doi: 10.1016/0040-8166(78)90009-5. [DOI] [PubMed] [Google Scholar]
- Humphreys W. J. The fine structure of cortical granules in eggs and gastrulae of Mytilus edulis. J Ultrastruct Res. 1967 Feb;17(3):314–326. doi: 10.1016/s0022-5320(67)80051-0. [DOI] [PubMed] [Google Scholar]
- Jaffe L. A. Fast block to polyspermy in sea urchin eggs is electrically mediated. Nature. 1976 May 6;261(5555):68–71. doi: 10.1038/261068a0. [DOI] [PubMed] [Google Scholar]
- Jaffe L. A., Gould-Somero M., Holland L. Ionic mechanism of the fertilization potential of the marine worm, Urechis caupo (Echiura). J Gen Physiol. 1979 Apr;73(4):469–492. doi: 10.1085/jgp.73.4.469. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johnson M., Edidin M. Lateral diffusion in plasma membrane of mouse egg is restricted after fertilisation. Nature. 1978 Mar 30;272(5652):448–450. doi: 10.1038/272448a0. [DOI] [PubMed] [Google Scholar]
- Johnston R. N., Paul M. Calcium influx following fertilization of Urechis caupo eggs. Dev Biol. 1977 Jun;57(2):364–374. doi: 10.1016/0012-1606(77)90221-4. [DOI] [PubMed] [Google Scholar]
- KEYNES R. D., SWAN R. C. The permeability of frog muscle fibres to lithium ions. J Physiol. 1959 Oct;147:626–638. doi: 10.1113/jphysiol.1959.sp006265. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kohlhardt M., Bauer B., Krause H., Fleckenstein A. Differentiation of the transmembrane Na and Ca channels in mammalian cardiac fibres by the use of specific inhibitors. Pflugers Arch. 1972;335(4):309–322. doi: 10.1007/BF00586221. [DOI] [PubMed] [Google Scholar]
- Kuroda T. The effects of D600 and verapamil on action potential in the X-organ neuron of the crayfish. Jpn J Physiol. 1976;26(2):189–202. doi: 10.2170/jjphysiol.26.189. [DOI] [PubMed] [Google Scholar]
- Lester H. A., Koblin D. D., Sheridan R. E. Role of voltage-sensitive receptors in nicotinic transmission. Biophys J. 1978 Mar;21(3):181–194. doi: 10.1016/S0006-3495(78)85518-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Longo F. J. Cortical changes in Spisula eggs upon insemination. J Ultrastruct Res. 1976 Aug;56(2):226–232. doi: 10.1016/s0022-5320(76)80168-2. [DOI] [PubMed] [Google Scholar]
- Longo F. J. Effects of cytochalasin B on sperm--egg interactions. Dev Biol. 1978 Dec;67(2):249–265. doi: 10.1016/0012-1606(78)90197-5. [DOI] [PubMed] [Google Scholar]
- MAENO T. Electrical characteristics and activation potential of Bufo eggs. J Gen Physiol. 1959 Sep;43:139–157. doi: 10.1085/jgp.43.1.139. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Mueller P. Membrane excitation through voltage-induced aggregation of channel precursors. Ann N Y Acad Sci. 1975 Dec 30;264:247–264. doi: 10.1111/j.1749-6632.1975.tb31487.x. [DOI] [PubMed] [Google Scholar]
- Nuccitelli R., Jaffe L. F. The ionic components of the current pulses generated by developing fucoid eggs. Dev Biol. 1976 Apr;49(2):518–531. doi: 10.1016/0012-1606(76)90193-7. [DOI] [PubMed] [Google Scholar]
- Papahadjopoulos D., Poste G., Schaeffer B. E. Fusion of mammalian cells by unilamellar lipid vesicles: inflluence of lipid surface charge, fluidity and cholesterol. Biochim Biophys Acta. 1973 Sep 27;323(1):23–42. doi: 10.1016/0005-2736(73)90429-x. [DOI] [PubMed] [Google Scholar]
- Paul M., Gould-Somero M. Evidence for a polyspermy block at the level of sperm-egg plasma membrane fusion in Urechis caupo. J Exp Zool. 1976 Apr;196(1):105–112. doi: 10.1002/jez.1401960110. [DOI] [PubMed] [Google Scholar]
- Paul M. Release of acid and changes in light-scattering properties following fertilization of Urechis caupo eggs. Dev Biol. 1975 Apr;43(2):299–312. doi: 10.1016/0012-1606(75)90029-9. [DOI] [PubMed] [Google Scholar]
- Paul M. The polyspermy block in eggs of Urechis caupo. Evidence for a "rapid" block. Exp Cell Res. 1975 Jan;90(1):137–142. doi: 10.1016/0014-4827(75)90366-3. [DOI] [PubMed] [Google Scholar]
- Peng H. B., Jaffe L. F. A simple, selective method for freeze-fracturing spherical cells. J Cell Biol. 1976 Nov;71(2):674–680. doi: 10.1083/jcb.71.2.674. [DOI] [PMC free article] [PubMed] [Google Scholar]
- REBHUN L. I. Electron microscope studies on the vitelline membrane of the surf clam, Spisula solidissima. J Ultrastruct Res. 1962 Feb;6:107–122. doi: 10.1016/s0022-5320(62)90064-3. [DOI] [PubMed] [Google Scholar]
- Rash J. E., Staehelin L. A. Freeze-cleave demonstration of gap junctions between skeletal myogenic cells in vivo. Dev Biol. 1974 Feb;36(2):455–461. doi: 10.1016/0012-1606(74)90066-9. [DOI] [PubMed] [Google Scholar]
- Rosati F., Monroy A., De Prisco P. Fine structural study of fertilization in the ascidian, Ciona intestinalis. J Ultrastruct Res. 1977 Mar;58(3):261–270. doi: 10.1016/s0022-5320(77)90018-1. [DOI] [PubMed] [Google Scholar]
- 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. 1976 Jan;48(1):148–162. doi: 10.1016/0012-1606(76)90053-1. [DOI] [PubMed] [Google Scholar]
- Weiss R. L., Goodenough D. A., Goodenough U. W. Membrane differentiations at sites specialized for cell fusion. J Cell Biol. 1977 Jan;72(1):144–160. doi: 10.1083/jcb.72.1.144. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wolf D. P. The block to sperm penetration in zonal-free mouse eggs. Dev Biol. 1978 May;64(1):1–10. doi: 10.1016/0012-1606(78)90056-8. [DOI] [PubMed] [Google Scholar]
- Ziomek C. A., Epel D. Polyspermy block of Spisula eggs is prevented by cytochalasin B. Science. 1975 Jul 11;189(4197):139–141. doi: 10.1126/science.1173469. [DOI] [PubMed] [Google Scholar]