抑制性寡核苷酸阻断刺激性CpG寡核苷酸在B细胞中对AP-1转录因子的诱导。

Petar Lenert, Ae-Kyung Yi, Arthur M Krieg, Laura L Stunz, Robert F Ashman
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引用次数: 29

摘要

原代B细胞对CpG寡核苷酸(ODN)的增殖反应涉及核活化促进-1 (AP-1)转录因子的诱导。AP-1亚基c-Fos、Fos-B、Jun-B和Jun-D均在刺激30分钟内被CpG ODNs诱导,Fra-1和Fra-2则不被诱导,c-Jun在刺激1-2小时后被诱导。c-Jun在6小时时达到最大值。40小时后,Jun-B和Jun-D占据了主导地位。人工合成的含有鸟苷三联体/四联体的odn,与富含5'嘧啶的单元保持适当距离,可抑制cpg驱动的细胞周期进入和凋亡保护,同时添加刺激性odn时可阻断AP-1诱导。刺激30分钟后,6小时时,添加抑制剂不再影响AP-1。没有AP-1亚基逃脱ODN抑制。在转染AP-1- β -半乳糖苷酶报告基因构建的细胞系中,抑制ODN可以阻止CpG ODN诱导的AP-1转录活性,但脂多糖(LPS)诱导的AP-1转录活性没有被抑制。这些数据表明,抑制性odn在AP-1诱导的近端阻断CpG odn驱动的信号通路。
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Inhibitory oligonucleotides block the induction of AP-1 transcription factor by stimulatory CpG oligonucleotides in B cells.

The proliferative response of primary B cells to CpG oligonucleotides (ODN) involves induction of nuclear activation promoting-1 (AP-1) transcription factor. AP-1 subunits c-Fos, Fos-B, Jun-B, and Jun-D, but not Fra-1 or Fra-2, were all induced by CpG ODNs in B cells within 30 minutes of stimulation, followed by c-Jun at 1-2 hours. c-Jun reached maximum at 6 hours. By 40 hours, Jun-B and Jun-D became dominant. Synthetic ODNs containing a single guanosine triplet/tetrad appropriately distanced from the 5' pyrimidine-rich unit, which inhibit CpG-driven cell cycle entry and apoptosis protection, blocked AP-1 induction by stimulatory ODNs when they were added simultaneously. After 30 minutes of stimulation, adding inhibitor no longer affected AP-1 at 6 hours. No AP-1 subunits escaped ODN inhibition. In a cell line transfected with an AP-1-beta-galactosidase reporter construct, CpG ODN-induced AP-1 transcriptional activity was prevented by inhibitory ODN, but lipopolysaccharide (LPS)-induced AP-1 activity was not. These data suggest that inhibitory ODNs block the CpG ODN-driven signaling pathway at a site proximal to AP-1 induction.

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