Cutting edge: tyk2 is required for the induction and nuclear translocation of Daxx which regulates IFN-alpha-induced suppression of B lymphocyte formation.

نویسندگان

  • Kazuya Shimoda
  • Kenjirou Kamesaki
  • Akihiko Numata
  • Kenichi Aoki
  • Tadashi Matsuda
  • Kenji Oritani
  • Sadafumi Tamiya
  • Kouji Kato
  • Ken Takase
  • Rie Imamura
  • Tetsuya Yamamoto
  • Toshihiro Miyamoto
  • Koji Nagafuji
  • Hisashi Gondo
  • Seiho Nagafuchi
  • Kei-Ichi Nakayama
  • Mine Harada
چکیده

IFN-alpha inhibits B lymphocyte development, and the nuclear protein Daxx has been reported to be essential for this biological activity. We show in this study that IFN-alpha inhibits the clonal proliferation of B lymphocyte progenitors in response to IL-7 in wild-type, but not in tyk2-deficient, mice. In addition, the IFN-alpha-induced up-regulation and nuclear translocation of Daxx are completely abrogated in the absence of tyk2. Therefore, tyk2 is directly involved in IFN-alpha signaling for the induction and translocation of Daxx, which may result in B lymphocyte growth arrest and/or apoptosis.

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عنوان ژورنال:
  • Journal of immunology

دوره 169 9  شماره 

صفحات  -

تاریخ انتشار 2002