S6 kinase 2 potentiates interleukin-3-driven cell proliferation

J Leukoc Biol. 2005 Dec;78(6):1378-85. doi: 10.1189/jlb.0405225. Epub 2005 Oct 4.

Abstract

Interleukin-3 (IL-3) mediates hematopoietic cell survival and proliferation via several signaling pathways such as the Janus kinase/signal transducer and activator of transcription pathway, mitogen-activated protein kinase (MAPK) pathway, and phosphoinositide-3 kinase (PI-3K) pathway. Mammalian target of rapamycin (mTOR) is one of the downstream targets of the PI-3K pathway, and it plays an important role in hematopoiesis and immune cell function. To better elucidate how mTOR mediates proliferation signals from IL-3, we assessed the role of S6 kinase 2 (S6K2), one of the downstream targets of mTOR, in IL-3 signaling. We show that S6K2 is activated by IL-3 in the IL-3-dependent Ba/F3 cell line and that this is mediated by mTOR and its upstream activator PI-3K but not by the MAPK kinase/extracellular signal-regulated kinase pathway. S6K2 is also activated in primary mouse bone marrow-derived mast cells upon IL-3 stimulation. Expression of a rapamycin-resistant form of S6K2, T388E, in Ba/F3 cells provides a proliferation advantage in the absence or presence of rapamycin, indicating that S6K2 can potentiate IL-3-mediated mitogenic signals. In cells expressing T388E, rapamycin still reduces proliferation at all doses of rapamycin, showing that mTOR targets other than S6K2 play an important role in IL-3-dependent proliferation. Cell-cycle analysis shows that T388E-expressing Ba/F3 cells enter S phase earlier than the control cells, indicating that the proliferation advantage may be mediated by a shortened G1 phase. This is the first indication that S6K2 plays a role in IL-3-dependent cell proliferation.

Publication types

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

MeSH terms

  • Animals
  • Bone Marrow Cells / drug effects
  • Bone Marrow Cells / enzymology*
  • Bone Marrow Cells / immunology
  • Cell Division / drug effects
  • Cell Division / immunology
  • Cell Line
  • Cell Proliferation / drug effects*
  • Cells, Cultured
  • Dose-Response Relationship, Drug
  • G1 Phase / drug effects
  • G1 Phase / immunology
  • Humans
  • Interleukin-3 / metabolism*
  • Interleukin-3 / pharmacology
  • Mast Cells / drug effects
  • Mast Cells / enzymology*
  • Mast Cells / immunology
  • Mice
  • Phosphatidylinositol 3-Kinases / drug effects
  • Phosphatidylinositol 3-Kinases / metabolism
  • Protein Kinases / metabolism*
  • Ribosomal Protein S6 Kinases, 90-kDa / drug effects
  • Ribosomal Protein S6 Kinases, 90-kDa / genetics
  • Ribosomal Protein S6 Kinases, 90-kDa / metabolism*
  • S Phase / drug effects
  • S Phase / immunology
  • Signal Transduction / drug effects
  • Signal Transduction / immunology
  • Sirolimus / pharmacology
  • TOR Serine-Threonine Kinases

Substances

  • Interleukin-3
  • Protein Kinases
  • MTOR protein, human
  • mTOR protein, mouse
  • Ribosomal Protein S6 Kinases, 90-kDa
  • TOR Serine-Threonine Kinases
  • ribosomal protein S6 kinase, 90kDa, polypeptide 3
  • Sirolimus