uPAR and cathepsin B-mediated compartmentalization of JNK regulates the migration of glioma-initiating cells

Stem Cell Res. 2014 May;12(3):716-29. doi: 10.1016/j.scr.2014.02.008. Epub 2014 Mar 12.

Abstract

In the present study, we investigated the effect of simultaneous downregulation of uPAR and cathepsin B (pUC), alone or in combination with radiation, on JNK-MAPK signaling pathway in regulating the migration of non-GICs (glioma-initiating cells) and GICs. The increase in the expression of p-JNK with pUC treatment was mostly localized to nucleus whereas increase in the expression of p-JNK with radiation and overexpression of uPAR and cathepsin B was confined to cytoplasm of the cells. Depletion of cytosolic p-JNK with pUC treatment inhibited migration by downregulating the expression of the adapter proteins of the focal adhesion complex. We also observed that knockdown of uPAR and cathepsin B regulated the Ras-Pak-1 pathway to induce the translocation of p-JNK from cytosol to nucleus. In control cells, Pak-1 served as a functional inhibitor for MEKK-1, which inhibits the complex formation of MEKK-1 and p-JNK and thus inhibits the translocation of this complex into nucleus. Hence, we conclude that glioma cells utilize the availability of cytosolic p-JNK in driving the cells towards migration. Finally, treating the cells with pUC alone or in combination with radiation induced the translocation of the MEKK-1-p-JNK complex from cytosol to nucleus, thereby inhibiting the migration of glioma cells.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Cathepsin B / genetics
  • Cathepsin B / metabolism*
  • Cell Movement*
  • Cell Nucleus / enzymology
  • Cell Nucleus / genetics
  • Cell Nucleus / metabolism
  • Cytoplasm / enzymology
  • Cytoplasm / genetics
  • Cytoplasm / metabolism
  • Cytosol / enzymology
  • Cytosol / metabolism
  • Female
  • Glioma / enzymology*
  • Glioma / genetics
  • Glioma / metabolism
  • Glioma / physiopathology
  • Humans
  • MAP Kinase Kinase 4 / genetics
  • MAP Kinase Kinase 4 / metabolism*
  • MAP Kinase Signaling System
  • Male
  • Mice
  • Protein Transport
  • Receptors, Urokinase Plasminogen Activator / genetics
  • Receptors, Urokinase Plasminogen Activator / metabolism*

Substances

  • Receptors, Urokinase Plasminogen Activator
  • MAP Kinase Kinase 4
  • Cathepsin B