Regulation of proapoptotic mammalian ste20-like kinase MST2 by the IGF1-Akt pathway

PLoS One. 2010 Mar 9;5(3):e9616. doi: 10.1371/journal.pone.0009616.

Abstract

Background: Hippo, a Drosophila serine/threonine kinase, promotes apoptosis and restricts cell growth and proliferation. Its mammalian homolog MST2 has been shown to play similar role and be regulated by Raf-1 via a kinase-independent mechanism and by RASSF family proteins through forming complex with MST2. However, regulation of MST2 by cell survival signal remains largely unknown.

Methodology/principal findings: Using immunoblotting, in vitro kinase and in vivo labeling assays, we show that IGF1 inhibits MST2 cleavage and activation induced by DNA damage through the phosphatidylinosotol 3-kinase (PI3K)/Akt pathway. Akt phosphorylates a highly conserved threonine-117 residue of MST2 in vitro and in vivo, which leads to inhibition of MST2 cleavage, nuclear translocation, autophosphorylation-Thr180 and kinase activity. As a result, MST2 proapoptotic and growth arrest function was significantly reduced. Further, inverse correlation between pMST2-T117/pAkt and pMST2-T180 was observed in human breast tumors.

Conclusions/significance: Our findings demonstrate for the first time that extracellular cell survival signal IGF1 regulates MST2 and that Akt is a key upstream regulator of MST2.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.
  • Retracted Publication

MeSH terms

  • Active Transport, Cell Nucleus
  • Animals
  • Breast Neoplasms / pathology
  • COS Cells
  • Caspase 3 / metabolism
  • Caspase 7 / metabolism
  • Cell Line
  • Chlorocebus aethiops
  • Gene Expression Regulation, Enzymologic*
  • Humans
  • Insulin-Like Growth Factor I / metabolism*
  • Phosphorylation
  • Protein Serine-Threonine Kinases / metabolism*
  • Proto-Oncogene Proteins c-akt / metabolism*
  • Serine-Threonine Kinase 3
  • Signal Transduction

Substances

  • Insulin-Like Growth Factor I
  • Protein Serine-Threonine Kinases
  • Proto-Oncogene Proteins c-akt
  • STK3 protein, human
  • Serine-Threonine Kinase 3
  • Caspase 3
  • Caspase 7