Literature DB >> 3491080

The part played by inositol trisphosphate and calcium in the propagation of the fertilization wave in sea urchin eggs.

K Swann, M Whitaker.   

Abstract

Sea urchin egg activation at fertilization is progressive, beginning at the point of sperm entry and moving across the egg with a velocity of 5 microns/s. This activation wave (Kacser, H., 1955, J. Exp. Biol., 32:451-467) has been suggested to be the result of a progressive release of calcium from a store within the egg cytoplasm (Jaffe, L. F., 1983, Dev. Biol., 99:265-276). The progressive release of calcium may be due to the production of inositol trisphosphate (InsP3), a second messenger. We show here that a wave of calcium release crosses the Lytechinus pictus egg; the peak of the wave travels with a velocity of 5 microns/s; microinjection of InsP3 causes the release of calcium within the egg; calcium release (as judged by fertilization envelope elevation) is abolished by prior injection of the calcium chelator EGTA; neomycin, an inhibitor of InsP3 production, does not prevent the release of calcium in response to InsP3 but does abolish the wave of calcium release; the egg cytoplasm rapidly buffers microinjected calcium; the calcium concentration required to cause fertilization membrane elevation when microinjected is very similar to that required to stimulate the production of InsP3 in vitro; and the progressive fertilization membrane elevation seen after microinjection of calcium buffers appears to be due to diffusion of the buffer across the egg cytoplasm rather than to the induction of the activation wave. We conclude that InsP3 diffuses through the egg cytoplasm much more readily than calcium ions and that calcium-stimulated production of InsP3 and InsP3-induced calcium release from an internal store can account for the progressive release of calcium at fertilization.

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Year:  1986        PMID: 3491080      PMCID: PMC2114628          DOI: 10.1083/jcb.103.6.2333

Source DB:  PubMed          Journal:  J Cell Biol        ISSN: 0021-9525            Impact factor:   10.539


  33 in total

1.  Physiological analysis of the cortical response of the sea urchin egg.

Authors:  M SUGIYAMA
Journal:  Exp Cell Res       Date:  1956-04       Impact factor: 3.905

2.  Effects of neomycin on calcium and polyphosphoinositide metabolism of guinea pig synaptosomes.

Authors:  H D Griffin; M Sykes; J N Hawthorne
Journal:  J Neurochem       Date:  1980-03       Impact factor: 5.372

3.  Prevention of the cortical reaction in fertilized sea urchin eggs by injection of calcium-chelating ligands.

Authors:  R S Zucker; R A Steinhardt
Journal:  Biochim Biophys Acta       Date:  1978-07-17

4.  Non-propagated cortical reactions induced by the divalent ionophore A23187 in eggs of the sea urchin, Lytechinus variegatus.

Authors:  E L Chambers; R E Hinkley
Journal:  Exp Cell Res       Date:  1979-12       Impact factor: 3.905

5.  Activation of sea urchin eggs by microinjection of calcium buffers.

Authors:  Y Hamaguchi; Y Hiramoto
Journal:  Exp Cell Res       Date:  1981-07       Impact factor: 3.905

Review 6.  Ionic regulation of egg activation.

Authors:  M J Whitaker; R A Steinhardt
Journal:  Q Rev Biophys       Date:  1982-11       Impact factor: 5.318

Review 7.  Intracellular pH.

Authors:  A Roos; W F Boron
Journal:  Physiol Rev       Date:  1981-04       Impact factor: 37.312

8.  Neutral carrier ion-selective microelectrodes for measurement of intracellular free calcium.

Authors:  R Y Tsien; T J Rink
Journal:  Biochim Biophys Acta       Date:  1980-07

9.  The relation between the increase in reduced nicotinamide nucleotides and the initiation of DNA synthesis in sea urchin eggs.

Authors:  M J Whitaker; R A Steinhardt
Journal:  Cell       Date:  1981-07       Impact factor: 41.582

10.  New calcium indicators and buffers with high selectivity against magnesium and protons: design, synthesis, and properties of prototype structures.

Authors:  R Y Tsien
Journal:  Biochemistry       Date:  1980-05-27       Impact factor: 3.162

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  38 in total

1.  Bombesin stimulation of inositol 1,4,5-trisphosphate generation and intracellular calcium release is amplified in a cell line overexpressing the N-ras proto-oncogene.

Authors:  A C Lloyd; S A Davies; I Crossley; M Whitaker; M D Houslay; A Hall; C J Marshall; M J Wakelam
Journal:  Biochem J       Date:  1989-06-15       Impact factor: 3.857

2.  Intracellular ion imaging using fluorescent dyes: artefacts and limits to resolution.

Authors:  R A Silver; M Whitaker; S R Bolsover
Journal:  Pflugers Arch       Date:  1992-04       Impact factor: 3.657

Review 3.  Calcium at fertilization and in early development.

Authors:  Michael Whitaker
Journal:  Physiol Rev       Date:  2006-01       Impact factor: 37.312

4.  The path of calcium in cytosolic calcium oscillations: a unifying hypothesis.

Authors:  L F Jaffe
Journal:  Proc Natl Acad Sci U S A       Date:  1991-11-01       Impact factor: 11.205

5.  Protein kinase C acts downstream of calcium at entry into the first mitotic interphase of Xenopus laevis.

Authors:  W M Bement; D G Capco
Journal:  Cell Regul       Date:  1990-02

6.  Comparison of Ca2+ mobilizing activities of cyclic ADP-ribose and inositol trisphosphate.

Authors:  P J Dargie; M C Agre; H C Lee
Journal:  Cell Regul       Date:  1990-02

7.  Reassociation of cortical secretory vesicles with sea urchin egg plasma membrane: assessment of binding specificity.

Authors:  R C Jackson; P A Modern
Journal:  J Membr Biol       Date:  1990-04       Impact factor: 1.843

8.  Some properties of the membrane currents underlying the fertilization potential in sea urchin eggs.

Authors:  C David; J Halliwell; M Whitaker
Journal:  J Physiol       Date:  1988-08       Impact factor: 5.182

9.  Okadaic acid suppresses calcium regulation of mitosis onset in sea urchin embryos.

Authors:  R Patel; M Whitaker
Journal:  Cell Regul       Date:  1991-05

10.  Guanosine 5'-thiotriphosphate may stimulate phosphoinositide messenger production in sea urchin eggs by a different route than the fertilizing sperm.

Authors:  I Crossley; T Whalley; M Whitaker
Journal:  Cell Regul       Date:  1991-02
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