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Cutting edge: tyk2 is required for the induction and nuclear translocation of Daxx which regulates IFN-alpha-induced suppression of B lymphocyte formation
Authors:Shimoda Kazuya  Kamesaki Kenjirou  Numata Akihiko  Aoki Kenichi  Matsuda Tadashi  Oritani Kenji  Tamiya Sadafumi  Kato Kouji  Takase Ken  Imamura Rie  Yamamoto Tetsuya  Miyamoto Toshihiro  Nagafuji Koji  Gondo Hisashi  Nagafuchi Seiho  Nakayama Kei-Ichi  Harada Mine
Affiliation:First Department of Internal Medicine, Faculty of Medicine, Kyushu University, Fukuoka, Japan. kshimoda@intmed1.med.kyushu-u.ac.jp
Abstract: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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