Literature DB >> 5690449

Oocyte differentiation in the sea urchin, Arbacia punctulata, with particular reference to the origin of cortical granules and their participation in the cortical reaction.

E Anderson.   

Abstract

This paper presents morphological evidence on the origin of cortical granules in the oocytes of Arbacia punctulata and other echinoderms. During oocyte differentiation, those Golgi complexes associated with the production of cortical granules are composed of numerous saccules with companion vesicles. Each element of the Golgi complex contains a rather dense homogeneous substance. The vesicular component of the Golgi complex is thought to be derived from the saccular member by a pinching-off process. The pinched-off vesicles are viewed as containers of the precursor(s) of the cortical granules. In time, they coalesce and form a mature cortical granule whose content is bounded by a unit membrane. Thus, it is asserted that the Golgi complex is involved in both the synthesis and concentration of precursors utilized in the construction of the cortical granule. Immediately after the egg is activated by the sperm the primary envelope becomes detached from the oolemma, thereby forming what we have called the activation calyx (see Discussion). Subsequent to the elaboration of the activation calyx, the contents of cortical granules are released (cortical reaction) into the perivitelline space. The discharge of the constituents of a cortical granule is accomplished by the union of its encompassing unit membrane, in several places, with the oolemma.

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Year:  1968        PMID: 5690449      PMCID: PMC2107408          DOI: 10.1083/jcb.37.2.514

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


  33 in total

1.  THE ANATOMY OF BOVINE AND OVINE PINEALS. LIGHT AND ELECTRON MICROSCOPIC STUDIES.

Authors:  E ANDERSON
Journal:  J Ultrastruct Res       Date:  1965-05

2.  The role of the cortical granules in the formation of the fertilization membrane in the eggs of sea urchins. II.

Authors:  Y ENDO
Journal:  Exp Cell Res       Date:  1961-12       Impact factor: 3.905

3.  Changes in the cortical layer of sea urchin eggs at fertilization as studied with the electron microscope. I. Clypeaster japonicus.

Authors:  Y ENDO
Journal:  Exp Cell Res       Date:  1961-11       Impact factor: 3.905

4.  Cortical granules in hamster eggs.

Authors:  C R AUSTIN
Journal:  Exp Cell Res       Date:  1956-04       Impact factor: 3.905

5.  Contribution to the study of germ-cells in the anura.

Authors:  A W BLACKLER
Journal:  J Embryol Exp Morphol       Date:  1958-09

6.  Development of cortical granules and the cortical reaction in rat and hamster eggs.

Authors:  D Szollosi
Journal:  Anat Rec       Date:  1967-12

7.  Changes in the ultrastructure of amphibian eggs following fertilization.

Authors:  B I Balinsky
Journal:  Acta Embryol Morphol Exp       Date:  1966-12

8.  The formation of the primary envelope during oocyte differentiation in teleosts.

Authors:  E Anderson
Journal:  J Cell Biol       Date:  1967-10       Impact factor: 10.539

9.  Improvements in epoxy resin embedding methods.

Authors:  J H LUFT
Journal:  J Biophys Biochem Cytol       Date:  1961-02

10.  Cytochemistry and electron microscopy. The preservation of cellular ultrastructure and enzymatic activity by aldehyde fixation.

Authors:  D D SABATINI; K BENSCH; R J BARRNETT
Journal:  J Cell Biol       Date:  1963-04       Impact factor: 10.539

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  38 in total

1.  Cell differentiation during early development of Nassarius reticulatus L. (Gastropoda Prosobranchia). I. Zygote to 16-cell stage.

Authors:  L Schmekel; P Fioroni
Journal:  Cell Tissue Res       Date:  1975-06-24       Impact factor: 5.249

2.  Turning on of activities in unfertilized sea urchin eggs: correlation with changes of the surface.

Authors:  D Mazia; G Schatten; R Steinhardt
Journal:  Proc Natl Acad Sci U S A       Date:  1975-11       Impact factor: 11.205

3.  Rendezvin: An essential gene encoding independent, differentially secreted egg proteins that organize the fertilization envelope proteome after self-association.

Authors:  Julian L Wong; Gary M Wessel
Journal:  Mol Biol Cell       Date:  2006-09-27       Impact factor: 4.138

4.  Concordance and interaction of guanine nucleotide dissociation inhibitor (RhoGDI) with RhoA in oogenesis and early development of the sea urchin.

Authors:  Vanesa Zazueta-Novoa; Guadalupe Martínez-Cadena; Gary M Wessel; Roberto Zazueta-Sandoval; Laura Castellano; Jesús García-Soto
Journal:  Dev Growth Differ       Date:  2011-04       Impact factor: 2.053

5.  Bipolar, anastral spindle development in artificially activated sea urchin eggs.

Authors:  John H Henson; Christopher A Fried; Mary K McClellan; Jason Ader; Jessica E Davis; Rudolf Oldenbourg; Calvin R Simerly
Journal:  Dev Dyn       Date:  2008-05       Impact factor: 3.780

Review 6.  Nucleolus precursor body (NPB): a distinct structure in mammalian oocytes and zygotes.

Authors:  Hirohisa Kyogoku; Tomoya S Kitajima; Takashi Miyano
Journal:  Nucleus       Date:  2014       Impact factor: 4.197

7.  Fertilization in fucus.

Authors:  E G Pollock
Journal:  Planta       Date:  1970-03       Impact factor: 4.116

8.  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

9.  Anatomy of the ovaries of the starfish Asterias rubens (Echinodermata). A histological and ultrastructural study.

Authors:  H J Schoenmakers; P H Colenbrander; J Peute; P G van Oordt
Journal:  Cell Tissue Res       Date:  1981       Impact factor: 5.249

10.  Occurrence and properties of a thermostable protease secreted by sea-urchin embryos.

Authors:  D Barrett
Journal:  Biochem J       Date:  1970-03       Impact factor: 3.857

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