Literature DB >> 5786981

A fine structural analysis of cleavage induction and furrowing in the eggs of Arbacia punctulata.

L G Tilney, D Marsland.   

Abstract

A fine structural study has been carried out on the various formed elements present before, during, and after the first cleavage division, not only in normally developing Arbacia eggs, but also in eggs which have been induced to cleave prematurely by high-pressure centrifugation. The aim has been to ascertain whether or not any of the morphologically identifiable components may be involved in initiating the furrowing process. Also, attention has been given to the fine structure of the cytoplasmic cortex, particulary in the walls of the furrow, in the hope of reaching a better understanding of the mechanics of cleavage. The annulate lamellae and the membranous envelope of the nucleus are the only formed elements which disappear shortly before cleavage, not only in eggs undergoing normal division, but also in eggs which have been induced to cleave ahead of schedule by high-pressure, high-force centrifugation. Therefore, it is suggested as a tentative hypothesis that materials liberated upon disintegration of the nuclear membrane and the annulate lamellae play an essential role in initiating and effecting the furrowing reaction, especially since the stratification of these elements in experimentally induced eggs corresponds to the position of the developing furrow. Another of the membranous elements in the egg, the Golgi complex, shows considerable modification as a result of high-pressure centrifugation, but these structures do not undergo disintegration. Rather, they become curled into rounded bodies. The vacuole population is not greatly affected by inducing treatments. During cleavage, both naturally occurring and experimentally induced, a considerable number of 50 A filaments appear in the denser cytoplasmic cortex, but only in the walls of the furrow. These filaments are similar to those which have been demonstrated in a number of contractile cells. Accordingly, it is suggested that this fibrillar system may be actively involved in the development of the cleavage force.

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Year:  1969        PMID: 5786981      PMCID: PMC2107580          DOI: 10.1083/jcb.42.1.170

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


  19 in total

1.  Cell division without mitotic apparatus in sea urchin eggs.

Authors:  Y HIRAMOTO
Journal:  Exp Cell Res       Date:  1956-12       Impact factor: 3.905

2.  Experiments concerning the cleavage furrow in invertebrate eggs.

Authors:  R Rappaport
Journal:  J Exp Zool       Date:  1966-02

Review 3.  Contractile properties of protein threads from sea urchin eggs in relation to cell division.

Authors:  H Sakai
Journal:  Int Rev Cytol       Date:  1968

4.  The behaviour and localization of intracellular relaxing system during cleavage in the sea urchin egg.

Authors:  S Kinoshita; I Yazaki
Journal:  Exp Cell Res       Date:  1967-09       Impact factor: 3.905

5.  The effects of selected chemical agents on furrow induction in the eggs of Arbacia punctualata.

Authors:  S B Zimmerman; T H Murakami; A M Zimmerman
Journal:  Biol Bull       Date:  1968-04       Impact factor: 1.818

6.  Light and electron microscope studies of smooth endoplasmic reticulum in dividing rat hepatic cells.

Authors:  W J Dougherty; M M Lee
Journal:  J Ultrastruct Res       Date:  1967-07

7.  Cytoplasmic filaments and cell movements: epidermal cells during ascidian metamorphosis.

Authors:  R A Cloney
Journal:  J Ultrastruct Res       Date:  1966-02

8.  Cytoplasmic filaments and morphogenetic movement in the amphibian neural tube.

Authors:  P C Baker; T E Schroeder
Journal:  Dev Biol       Date:  1967-05       Impact factor: 3.582

9.  Structural organization associated with pseudopod extension and contraction during cell locomotion in Difflugia.

Authors:  A Wohlman; R D Allen
Journal:  J Cell Sci       Date:  1968-03       Impact factor: 5.285

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

Authors:  E Anderson
Journal:  J Cell Biol       Date:  1968-05       Impact factor: 10.539

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  16 in total

1.  Effect of cell-surface binding on development of Ascidian egg.

Authors:  Marko Zalokar
Journal:  Wilehm Roux Arch Dev Biol       Date:  1979-03

2.  Ultrastructure of a fertilized barnacle egg (Pollicipes polymerus) with peristaltic constrictions.

Authors:  Cindy Arey Lewis
Journal:  Wilehm Roux Arch Dev Biol       Date:  1977-12

3.  Localization of serotonin in cleavage embryos of Ophryotrocha labronica La Greca and Bacci.

Authors:  Hadar Emanuelsson
Journal:  Wilhelm Roux Arch Entwickl Mech Org       Date:  1974-12

4.  Actin in the brush-border of epithelial cells of the chicken intestine.

Authors:  L G Tilney; M Mooseker
Journal:  Proc Natl Acad Sci U S A       Date:  1971-10       Impact factor: 11.205

5.  Preparation and purification of polymerized actin from sea urchin egg extracts.

Authors:  R E Kane
Journal:  J Cell Biol       Date:  1975-08       Impact factor: 10.539

6.  The contractile ring. II. Determining its brief existence, volumetric changes, and vital role in cleaving Arbacia eggs.

Authors:  T E Schroeder
Journal:  J Cell Biol       Date:  1972-05       Impact factor: 10.539

7.  Wave of stiffness propagating along the surface of the newt egg during cleavage.

Authors:  T Sawai; M Yoneda
Journal:  J Cell Biol       Date:  1974-01       Impact factor: 10.539

8.  Effect of microinjected N-ethylmaleimide-modified heavy meromyosin on cell division in amphibian eggs.

Authors:  R L Meeusen; J Bennett; W Z Cande
Journal:  J Cell Biol       Date:  1980-09       Impact factor: 10.539

9.  Evidence for RNA in the heavy bodies of sea urchin eggs.

Authors:  C M Conway
Journal:  J Cell Biol       Date:  1971-12       Impact factor: 10.539

10.  New membrane formation during cytokinesis in normal and cytochalasin B-treated eggs of Xenopus laevis. I. Electron microscope observations.

Authors:  J G Bluemink; S W de Laat
Journal:  J Cell Biol       Date:  1973-10       Impact factor: 10.539

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