Role of intercellular contacts in generating an asymmetric mitotic apparatus in the Tubifex embryo

Dev Growth Differ. 1997 Jun;39(3):351-62. doi: 10.1046/j.1440-169x.1997.t01-2-00011.x.

Abstract

The 2-cell stage embryo of Tubifex is composed of a smaller cell, AB, and a larger cell, CD. At the second cleavage, the CD-cell divides unequally. The mitotic apparatus (MA) involved in this division is organized asymmetrically: the MA pole to be segregated to a smaller cell is flattened and truncated, and associated with the anterior cortex facing the AB-cell, while the other pole is symmetric and located more centrally. The present study was undertaken to elucidate the mechanism that generates asymmetry in the MA organization in CD-cells. When CD-cell nuclei, which are normally located near the anterior cortex, were displaced toward the posterior end of the cell (i.e. opposite AB-cells) by centrifugation, MA assembled ectopically there, and were bilaterally symmetric in organization. Similar symmetric MA were formed in isolated CD-cells, which divided more equally than intact cells. This equality of cell division was dramatically reduced if the anterior surface of isolated CD-cells formed contact with other cells, such as AB-, C- and 4D-cells. The MA that formed in these reconstituted embryos were asymmetric in organization; one MA pole was always found to be truncated and apposed to the cortical site at the cell contact. Symmetric MA were also observed in cytochalasin-treated embryos. Together with the finding that one of the MA poles is physically attached to the anterior cortex of the intact CD-cell, these results suggest that factors generating asymmetry in the spatial organization of MA poles reside at the anterior cortex of the CD-cell and that this cortical mechanism is dependent upon cell contacts.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Caenorhabditis elegans / embryology
  • Cell Adhesion
  • Cell Division
  • Cell Separation
  • Cell Size
  • Cytochalasin D / pharmacology
  • Cytoskeleton / drug effects
  • Cytoskeleton / ultrastructure
  • Intercellular Junctions / ultrastructure
  • Oligochaeta / cytology
  • Oligochaeta / embryology*
  • Oligochaeta / ultrastructure
  • Species Specificity
  • Spindle Apparatus / drug effects
  • Spindle Apparatus / ultrastructure

Substances

  • Cytochalasin D