Mammalian spindle orientation and position respond to changes in cell shape in a dynein-dependent fashion

Mol Biol Cell. 2000 May;11(5):1765-74. doi: 10.1091/mbc.11.5.1765.

Abstract

In animal cells, positioning of the mitotic spindle is crucial for defining the plane of cytokinesis and the size ratio of daughter cells. We have characterized this phenomenon in a rat epithelial cell line using microscopy, micromanipulation, and microinjection. Unmanipulated cells position the mitotic spindle near their geometric center, with the spindle axis lying roughly parallel to the long axis of the cell. Spindles that were initially misoriented underwent directed rotation and caused a delay in anaphase onset. To gain further insight into this process, we gently deformed cells with a blunted glass needle to change the spatial relationship between the cortex and spindle. This manipulation induced spindle movement or rotation in metaphase and/or anaphase, until the spindle reached a proper position relative to the deformed shape. Spindle positioning was inhibited by either treatment with low doses of nocodazole or microinjection of antibodies against dynein, apparently due to the disruption of the organization of dynein and/or astral microtubules. Our results suggest that mitotic cells continuously monitor and maintain the position of the spindle relative to the cortex. This process is likely driven by interactions among astral microtubules, the motor protein dynein, and the cell cortex and may constitute part of a mitotic checkpoint mechanism.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Size / drug effects
  • Cells, Cultured
  • Dyneins / metabolism*
  • Kidney / cytology*
  • Microinjections
  • Micromanipulation
  • Microtubules / metabolism
  • Mitosis
  • Nocodazole / pharmacology
  • Rats
  • Spindle Apparatus / drug effects
  • Spindle Apparatus / metabolism*
  • Spindle Apparatus / ultrastructure*

Substances

  • Dyneins
  • Nocodazole