Literature DB >> 319914

Sequential biochemical and morphological events during assembly of the fertilization membrane of the sea urchin.

M Veron, C Foerder, E M Eddy.   

Abstract

The fertilization membrane of Strongylocentrotus purpuratus undergoes changes in morphology, solubility, and permeability during the process of hardening. As the fertilization membrane elevates from the egg surface, it retains casts of the tips of the microvillous processes of the plasma membrane. The dome-shaped microvillar casts become angular at the same time that the fertilization membrane becomes resistant to solubilization in mercaptan solutions. 2-4 min after this morphological and chemical transition, the fertilization membrane becomes impermeable to the lectin conconavalin A, as monitored by binding of 125I- or fluorescein-labeled concanavalin A. Glycine ethyl ester inhibits the changes in morphology, solubility, and permeability, whereas sodium sulfite inhibits only the permeability block and resistance to solubilization by mercaptans. Parthenogenetic activation with the divalent ionophore, A23187, elicits fertilization membrane elevation more rapidly than does activation by fertilization; however, the morphological and permeability changes characteristic of hardening proceed more slowly. Elevation and hardening of the fertilization membrane thus appear to be discrete, multiple-step assembly processes that occur in fixed sequence, with kinetics that are affected by the mechanism of cortical granule exocytosis.

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Year:  1977        PMID: 319914     DOI: 10.1016/0092-8674(77)90226-4

Source DB:  PubMed          Journal:  Cell        ISSN: 0092-8674            Impact factor:   41.582


  17 in total

1.  Extracellular matrix modifications at fertilization: regulation of dityrosine crosslinking by transamidation.

Authors:  Julian L Wong; Gary M Wessel
Journal:  Development       Date:  2009-04-29       Impact factor: 6.868

2.  Extracellular coats on the surface of Strongylocentrotus purpuratus eggs: stereo electron microscopy of quick-frozen and deep-etched specimens.

Authors:  D E Chandler; C J Kazilek
Journal:  Cell Tissue Res       Date:  1986       Impact factor: 5.249

3.  Changes in holding and ion-channel currents during activation of an ascidian egg under voltage clamp.

Authors:  M Kozuka; K Takahashi
Journal:  J Physiol       Date:  1982-02       Impact factor: 5.182

4.  Hydrogen peroxide production, chemiluminescence, and the respiratory burst of fertilization: interrelated events in early sea urchin development.

Authors:  C A Foerder; S J Klebanoff; B M Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1978-07       Impact factor: 11.205

5.  Release of ovoperoxidase from sea urchin eggs hardens the fertilization membrane with tyrosine crosslinks.

Authors:  C A Foerder; B M Shapiro
Journal:  Proc Natl Acad Sci U S A       Date:  1977-10       Impact factor: 11.205

6.  Metabolic similarities between fertilization and phagocytosis. Conservation of a peroxidatic mechanism.

Authors:  S J Klebanoff; C A Foerder; E M Eddy; B M Shapiro
Journal:  J Exp Med       Date:  1979-04-01       Impact factor: 14.307

7.  Isolation and partial characterization of the plasma membrane of the sea urchin egg.

Authors:  W H Kinsey; G L Decker; W J Lennarz
Journal:  J Cell Biol       Date:  1980-10       Impact factor: 10.539

8.  Regulation of extracellular matrix assembly: in vitro reconstitution of a partial fertilization envelope from isolated components.

Authors:  P J Weidman; B M Shapiro
Journal:  J Cell Biol       Date:  1987-07       Impact factor: 10.539

9.  Actin, microvilli, and the fertilization cone of sea urchin eggs.

Authors:  L G Tilney; L A Jaffe
Journal:  J Cell Biol       Date:  1980-12       Impact factor: 10.539

10.  Assembly of the sea urchin fertilization membrane: isolation of proteoliaisin, a calcium-dependent ovoperoxidase binding protein.

Authors:  P J Weidman; E S Kay; B M Shapiro
Journal:  J Cell Biol       Date:  1985-03       Impact factor: 10.539

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