Cell death provoked by loss of interleukin-3 signaling is independent of Bad, Bim, and PI3 kinase, but depends in part on Puma

Blood. 2006 Sep 1;108(5):1461-8. doi: 10.1182/blood-2006-03-014209. Epub 2006 May 16.

Abstract

Growth and survival of hematopoietic cells is regulated by growth factors and cytokines, such as interleukin 3 (IL-3). When cytokine is removed, cells dependent on IL-3 kill themselves by a mechanism that is inhibited by overexpression of Bcl-2 and is likely to be mediated by proapoptotic Bcl-2 family members. Bad and Bim are 2 such BH3-only Bcl-2 family members that have been implicated as key initiators in apoptosis following growth factor withdrawal, particularly in IL-3-dependent cells. To test the role of Bad, Bim, and other proapoptotic Bcl-2 family members in IL-3 withdrawal-induced apoptosis, we generated IL-3-dependent cell lines from mice lacking the genes for Bad, Bim, Puma, both Bad and Bim, and both Bax and Bak. Surprisingly, Bad was not required for cell death following IL-3 withdrawal, suggesting changes to phosphorylation of Bad play only a minor role in apoptosis in this system. Deletion of Bim also had no effect, but cells lacking Puma survived and formed colonies when IL-3 was restored. Inhibition of the PI3 kinase pathway promoted apoptosis in the presence or absence of IL-3 and did not require Bad, Bim, or Puma, suggesting IL-3 receptor survival signals and PI3 kinase survival signals are independent.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis Regulatory Proteins / deficiency
  • Apoptosis Regulatory Proteins / physiology*
  • Bcl-2-Like Protein 11
  • Cell Death / physiology*
  • Cell Division
  • Cell Line
  • Cell Survival / physiology*
  • Interleukin-3 / pharmacology
  • Interleukin-3 / physiology*
  • Membrane Proteins / deficiency
  • Membrane Proteins / physiology*
  • Mice
  • Mice, Knockout
  • Phosphatidylinositol 3-Kinases / physiology*
  • Proto-Oncogene Proteins / deficiency
  • Proto-Oncogene Proteins / physiology*
  • Signal Transduction
  • Tumor Suppressor Proteins / deficiency
  • Tumor Suppressor Proteins / physiology*
  • bcl-2-Associated X Protein / deficiency
  • bcl-2-Associated X Protein / physiology
  • bcl-Associated Death Protein / deficiency
  • bcl-Associated Death Protein / physiology*

Substances

  • Apoptosis Regulatory Proteins
  • Bax protein, mouse
  • Bcl-2-Like Protein 11
  • Bcl2l11 protein, mouse
  • Interleukin-3
  • Membrane Proteins
  • PUMA protein, mouse
  • Proto-Oncogene Proteins
  • Tumor Suppressor Proteins
  • bcl-2-Associated X Protein
  • bcl-Associated Death Protein
  • Phosphatidylinositol 3-Kinases