Activation of Tyk2 and Stat3 is required for the apoptotic actions of interferon-beta in primary pro-B cells

J Biol Chem. 2006 Jun 16;281(24):16238-44. doi: 10.1074/jbc.M509516200. Epub 2006 Apr 6.

Abstract

The growth-inhibitory effects of type 1 interferons (IFNs) (IFNalpha/beta) are complex, and the role of apoptosis in their antigrowth effects is variable and not well understood. We have examined primary murine interleukin-7-dependent bone marrow-derived pro-B cells, where IFNbeta, but not IFNalpha, induces programmed cell death (PCD). IFNbeta-stimulated apoptosis is the same in pro-B cells derived from wild type and Stat1(-/-) mice. However, in pro-B cells from Tyk2(-/-) mice, where there is normal activation of Stat1 and Stat2, IFNbeta-stimulated PCD is not observed. Loss of B cells in lymphocytic choriomeningitis virus-infected mice has been shown to be mediated through the expression of IFNalpha/beta (1). In wild type mice infected with lymphocytic choriomeningitis virus, there is a greater loss of B cells in the bone marrow and spleen than in Tyk2(-/-) mice infected with the virus, suggesting that the expression of this kinase plays an in vivo role in IFNalpha/beta-mediated PCD. In contrast to IFNbeta-stimulated tyrosine phosphorylation of Stat1 and Stat2, Stat3 tyrosine phosphorylation is defective in Tyk2(-/-) pro-B cells, suggesting that this Stat family member is required for apoptosis. In support of this hypothesis, inhibition of Stat3 activation in wild type B cells reverses the apoptotic effects of IFNbeta. Furthermore, expression of a constitutively active form of Stat3 in Tyk2(-/-) B cells partially restores IFNbeta-stimulated PCD. These results demonstrate an important role of Tyk2-mediated tyrosine phosphorylation of Stat3 in the ability of IFNbeta to stimulate apoptosis of primary pro-B cells.

MeSH terms

  • Animals
  • Annexin A5 / metabolism
  • Apoptosis
  • B-Lymphocytes / metabolism*
  • Cytoplasm / metabolism
  • Immunoblotting
  • Interferon-beta / metabolism*
  • Interleukin-7 / metabolism
  • Mice
  • Mice, Transgenic
  • Phosphorylation
  • Protein-Tyrosine Kinases / chemistry*
  • STAT3 Transcription Factor / metabolism*
  • TYK2 Kinase
  • Tyrosine / chemistry

Substances

  • Annexin A5
  • Interleukin-7
  • STAT3 Transcription Factor
  • Tyrosine
  • Interferon-beta
  • Protein-Tyrosine Kinases
  • TYK2 Kinase
  • Tyk2 protein, mouse