Interleukin-4-mediated protection of primary B cells from apoptosis through Stat6-dependent up-regulation of Bcl-xL

J Biol Chem. 2002 Jul 26;277(30):27169-75. doi: 10.1074/jbc.M201207200. Epub 2002 May 22.

Abstract

Apoptosis is an integral aspect of B lymphocyte development and homeostasis and is regulated by the engagement of antigen costimulatory and cytokine receptors. Although it is well established that interleukin 4 (IL-4) is a potent anti-apoptotic cytokine for B lymphocytes, little is known about the IL-4-induced molecular events regulating cell survival. Stat6 is rapidly activated after IL-4 stimulation, but its role in B lymphocyte apoptosis has not been explored. In this report we demonstrate that Stat6 is a critical signaling molecule for IL-4 in protecting primary B cells from passive and Fas-induced cell death. We show that expression of the Bcl-2 family member, Bcl-xL, is induced maximally by IL-4 and anti-IgM/IL-4 in a Stat6-dependent manner. Additionally, we demonstrate that bcl-xL transcription is likely to be directly activated through a Stat6 binding site in the bcl-xL-flanking region. Finally, reconstitution of Stat6-deficient splenic B cells with Bcl-xL was able to protect those cells from Fas-induced cell death. These results suggest that the anti-apoptotic activity of IL-4 in B cells is mediated through the activation of Stat6 and subsequent transcription of Bcl-xL.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Apoptosis*
  • B-Lymphocytes / metabolism*
  • Blotting, Northern
  • Cell Death
  • Cells, Cultured
  • Immunoblotting
  • Interleukin-4 / metabolism*
  • Luciferases / metabolism
  • Lymphocytes / metabolism
  • Mice
  • Promoter Regions, Genetic
  • Propidium / pharmacology*
  • Protein Binding
  • Proto-Oncogene Proteins c-bcl-2 / metabolism*
  • Retroviridae / genetics
  • STAT6 Transcription Factor
  • Signal Transduction
  • Time Factors
  • Trans-Activators / metabolism*
  • Transcription, Genetic
  • Transfection
  • Up-Regulation*
  • bcl-X Protein

Substances

  • Bcl2l1 protein, mouse
  • Proto-Oncogene Proteins c-bcl-2
  • STAT6 Transcription Factor
  • Stat6 protein, mouse
  • Trans-Activators
  • bcl-X Protein
  • Interleukin-4
  • Propidium
  • Luciferases