Literature DB >> 1120334

Aspects of furrow membrane formation in the cleaving Drosophila embryo.

E J Sanders.   

Abstract

During blastoderm formation, the Drosophila embryo produces a large area of new membrane to accommodate the simultaneous demands of approximately four thousand newly cleaved cells. The embryo was examined with the electron microscope at various stages during cleavage in order to investigate the high membrane forming capacity of these cells. Embryos were subjected to the histochemical procedure for the demonstration of thiamine pyrophosphatase. The enzyme was present in the cisternae of the endoplasmic reticulum, Golgi bodies and the nuclear envelope. No activity could be demonstrated on the furrow surface or at the furrow tip despite closely adjacent reactive cisternae. It is concluded that the endoplasmic reticulum and Golgi bodies are not major contributors to the new surface. Lamellar bodies were frequently observed in the cytoplasm of all stages examined. The bodies showed a lamellar periodicity of approximately 3.5 nm, and were ultrastructurally similar in appearance after a variety of fixation procedures. The distribution of these bodies was markedly related to the stage of blastoderm formation. Before the commencement of cleavage, lamellar bodies were very prominent within a region 4--5 mum below the cell surface. As cleavage progressed, the bodies became sparse or absent from this region but were apparent at the base of the blastoderm cells or in the sub-blastoderm region, where they were not previously present. Lamellar bodies with leaflets closely associated with, or in apparent continuity with, the cleavage furrow membrane were frequently observed. In these regions the lamellar periodicity was the same as the thickness of the membrane laminae. It is suggested that these bodies play a role in the synthesis of new membrane in the furrow. Intercellular contact specializations between the developing membranes of the furrow were restricted to incipient desmosones and point contacts where the intercellular gap was reduced to 3 nm or less.

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Year:  1975        PMID: 1120334     DOI: 10.1007/bf00225106

Source DB:  PubMed          Journal:  Cell Tissue Res        ISSN: 0302-766X            Impact factor:   5.249


  27 in total

1.  ULTRASTRUCTURAL DIFFERENTIATIONS DURING FORMATION OF THE BLASTODERM IN THE DROSOPHILA MELANOGASTER EMBRYO.

Authors:  A P MAHOWALD
Journal:  Dev Biol       Date:  1963-10       Impact factor: 3.582

2.  ELECTRON MICROSCOPY OF THE FORMATION OF THE CELLULAR BLASTODERM IN DROSOPHILA MELANOGASTER.

Authors:  A P MAHOWALD
Journal:  Exp Cell Res       Date:  1963-12       Impact factor: 3.905

3.  ELECTRON MICROSCOPIC OBSERVATIONS OF YOUNG RAT LIVER. I. DISTRIBUTION AND STRUCTURE OF THE MYELIN FIGURES (LAMELLAR BODIES).

Authors:  A CECIO
Journal:  Z Zellforsch Mikrosk Anat       Date:  1964-05-29

4.  The submicroscopic structure of the Drosophila egg.

Authors:  E OKADA; C H WADDINGTON
Journal:  J Embryol Exp Morphol       Date:  1959-12

5.  An ultrastructural study of the first cleavage of Xenopus embryos.

Authors:  P K Singal; E J Sanders
Journal:  J Ultrastruct Res       Date:  1974-06

6.  Intercellular contact in the unincubated chick embryo.

Authors:  E J Sanders
Journal:  Z Zellforsch Mikrosk Anat       Date:  1973-08-14

7.  The biological significance of turnover of the surface membrane of animal cells.

Authors:  L Warren
Journal:  Curr Top Dev Biol       Date:  1969       Impact factor: 4.897

8.  Cytodifferentiation in the Rana pipiens oocyte. IV. Ultrastructural localization of thiamine pyrophosphatase and horseradish peroxidase.

Authors:  R G Kessel; R S Decker
Journal:  Z Zellforsch Mikrosk Anat       Date:  1972

9.  Cytokinesis and cytochalasin-induced furrow regression in the first-cleavage zygote of Xenopus laevis.

Authors:  J G Bluemink
Journal:  Z Zellforsch Mikrosk Anat       Date:  1971

10.  Lamellar bodies in oocytes of Xenopus laevis and their relation to the mode of fixation.

Authors:  U M Spornitz
Journal:  Experientia       Date:  1973-05-15
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  7 in total

1.  Intercellular junctions during development and in tissue cultures ofDrosophila melanogaster: An electron-microscopic study.

Authors:  Susann Eichenberger-Glinz
Journal:  Wilehm Roux Arch Dev Biol       Date:  1979-12

2.  Types and distribution of lamellar bodies in first cleavage Xenopus embryos.

Authors:  P K Singal
Journal:  Cell Tissue Res       Date:  1975-11-07       Impact factor: 5.249

3.  Cell membrane formation during the cellularization of the syncytial blastoderm of Drosophila.

Authors:  D Loncar; S J Singer
Journal:  Proc Natl Acad Sci U S A       Date:  1995-03-14       Impact factor: 11.205

4.  armadillo, bazooka, and stardust are critical for early stages in formation of the zonula adherens and maintenance of the polarized blastoderm epithelium in Drosophila.

Authors:  H A Müller; E Wieschaus
Journal:  J Cell Biol       Date:  1996-07       Impact factor: 10.539

5.  The synaptic protein syntaxin1 is required for cellularization of Drosophila embryos.

Authors:  R W Burgess; D L Deitcher; T L Schwarz
Journal:  J Cell Biol       Date:  1997-08-25       Impact factor: 10.539

6.  Lava lamp, a novel peripheral golgi protein, is required for Drosophila melanogaster cellularization.

Authors:  J C Sisson; C Field; R Ventura; A Royou; W Sullivan
Journal:  J Cell Biol       Date:  2000-11-13       Impact factor: 10.539

7.  Actin cytoskeleton remodeling during early Drosophila furrow formation requires recycling endosomal components Nuclear-fallout and Rab11.

Authors:  Blake Riggs; Wendy Rothwell; Sarah Mische; Gilles R X Hickson; Johanne Matheson; Thomas S Hays; Gwyn W Gould; William Sullivan
Journal:  J Cell Biol       Date:  2003-10-06       Impact factor: 10.539

  7 in total

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