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Phosphatidic acid-mediated mitogenic activation of mTOR signaling.

The mammalian target of rapamycin (mTOR) governs cell growth and proliferation by mediating the mitogen- and nutrient-dependent signal transduction that regulates messenger RNA translation. We identified phosphatidic acid (PA) as a critical component of mTOR signaling. In our study, mitogenic stimulation of mammalian cells led to a phospholipase D-dependent accumulation of cellular PA, which was required for activation of mTOR downstream effectors. PA directly interacted with the domain in mTOR that is targeted by rapamycin, and this interaction was positively correlated with mTOR's ability to activate downstream effectors. The involvement of PA in mTOR signaling reveals an important function of this lipid in signal transduction and protein synthesis, as well as a direct link between mTOR and mitogens. Furthermore, these studies suggest a potential mechanism for the in vivo actions of the immunosuppressant rapamycin.

Pubmed ID: 11729323


  • Fang Y
  • Vilella-Bach M
  • Bachmann R
  • Flanigan A
  • Chen J


Science (New York, N.Y.)

Publication Data

November 30, 2001

Associated Grants

  • Agency: NIGMS NIH HHS, Id: GM58064

Mesh Terms

  • Adaptor Proteins, Signal Transducing
  • Butanols
  • Carrier Proteins
  • Cell Line
  • Culture Media, Serum-Free
  • Enzyme Activation
  • Humans
  • Immunosuppressive Agents
  • Mitogens
  • Phosphatidic Acids
  • Phosphatidylinositol 3-Kinases
  • Phospholipase D
  • Phosphoproteins
  • Phosphorylation
  • Protein Binding
  • Protein Kinases
  • Protein Structure, Tertiary
  • Ribosomal Protein S6 Kinases
  • Signal Transduction
  • Sirolimus
  • TOR Serine-Threonine Kinases
  • Time Factors