共 59 条
CpG inhibits IgE class switch recombination through suppression of NFκB activity, but not through Id2 or Bcl6
被引:37
作者:
Kusunoki, T
Sugai, M
Gonda, H
Nambu, Y
Nagata-Nakajima, N
Katakai, T
Kusunoki, M
Sakamoto, A
Takeshisa, TD
Nakahata, T
Yokota, Y
Shimizu, A
机构:
[1] Kyoto Univ, Ctr Mol Biol & Genet, Sakyo Ku, Kyoto 6068507, Japan
[2] Kyoto Univ, Grad Sch Med, Dept Pediat, Sakyo Ku, Kyoto 6068507, Japan
[3] Kyoto Univ Hosp, Translat Res Ctr, Kyoto 6068507, Japan
[4] Chiba Univ, Grad Sch Med, Dept Dev Genet H2, Chuo Ku, Chiba 2608670, Japan
[5] Univ Fukui, Sch Med, Dept Mol Genet, Matsuoka, Fukui 9101193, Japan
关键词:
IRF4;
T-bet;
germline transcript;
IL-4;
D O I:
10.1016/j.bbrc.2004.12.192
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 [生物化学与分子生物学];
081704 [应用化学];
摘要:
The CpG motif in DNA plays a critical role in immunity via modulating the Th1/Th2 balance. In B cells, CpG-containing oligodcoxynucleotides (CpG ODNs) inhibit IL-4-mediated class switch recombination (CSR) to IgG1 and IgE through inhibition of the germline transcription (GLT) of these isotypes. However, the molecular mechanism of this inhibitory effect remains elusive. We showed here that Id2 and Bc16, both of which inhibit IgE GLT and CSR, are not involved in this inhibitory pathway. We demonstrated that there is reduced activity of NFkappaB binding to the IgE promoter and a reduction of Irf4 protein in CpG ODN-treated B cells. These data indicate the critical role of NFkappaB and Irf4 in the regulation of IgE CSR through actions downstream of CpG signaling. (C) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:499 / 506
页数:8
相关论文

