SLK-dependent activation of ERMs controls LGN-NuMA localization and spindle orientation

J Cell Biol. 2014 Jun 23;205(6):791-9. doi: 10.1083/jcb.201401049.

Abstract

Mitotic spindle orientation relies on a complex dialog between the spindle microtubules and the cell cortex, in which F-actin has been recently implicated. Here, we report that the membrane-actin linkers ezrin/radixin/moesin (ERMs) are strongly and directly activated by the Ste20-like kinase at mitotic entry in mammalian cells. Using microfabricated adhesive substrates to control the axis of cell division, we found that the activation of ERMs plays a key role in guiding the orientation of the mitotic spindle. Accordingly, impairing ERM activation in apical progenitors of the mouse embryonic neocortex severely disturbed spindle orientation in vivo. At the molecular level, ERM activation promotes the polarized association at the mitotic cortex of leucine-glycine-asparagine repeat protein (LGN) and nuclear mitotic apparatus (NuMA) protein, two essential factors for spindle orientation. We propose that activated ERMs, together with Gαi, are critical for the correct localization of LGN-NuMA force generator complexes and hence for proper spindle orientation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, Nuclear / analysis
  • Antigens, Nuclear / metabolism*
  • Cell Cycle Proteins
  • Cell Division
  • Cytoskeletal Proteins / metabolism
  • HeLa Cells
  • Humans
  • Intracellular Signaling Peptides and Proteins / analysis
  • Intracellular Signaling Peptides and Proteins / metabolism*
  • Membrane Proteins / metabolism
  • Microfilament Proteins / metabolism
  • Nuclear Matrix-Associated Proteins / analysis
  • Nuclear Matrix-Associated Proteins / metabolism*
  • Phosphorylation
  • Protein Serine-Threonine Kinases / analysis
  • Protein Serine-Threonine Kinases / metabolism
  • Protein Serine-Threonine Kinases / physiology*
  • Spindle Apparatus / metabolism*

Substances

  • Antigens, Nuclear
  • Cell Cycle Proteins
  • Cytoskeletal Proteins
  • GPSM2 protein, human
  • Intracellular Signaling Peptides and Proteins
  • Membrane Proteins
  • Microfilament Proteins
  • NUMA1 protein, human
  • Nuclear Matrix-Associated Proteins
  • ezrin
  • moesin
  • radixin
  • SLK protein, human
  • Protein Serine-Threonine Kinases