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抑制性寡核苷酸可阻断B细胞中刺激性CpG寡核苷酸对AP-1转录因子的诱导作用。

Inhibitory oligonucleotides block the induction of AP-1 transcription factor by stimulatory CpG oligonucleotides in B cells.

作者信息

Lenert Petar, Yi Ae-Kyung, Krieg Arthur M, Stunz Laura L, Ashman Robert F

机构信息

Department of Internal Medicine, University of Iowa, College of Medicine, Iowa City, IA 52242, USA.

出版信息

Antisense Nucleic Acid Drug Dev. 2003;13(3):143-50. doi: 10.1089/108729003768247600.

Abstract

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.

摘要

原代B细胞对CpG寡核苷酸(ODN)的增殖反应涉及核激活促进因子-1(AP-1)转录因子的诱导。AP-1亚基c-Fos、Fos-B、Jun-B和Jun-D,而非Fra-1或Fra-2,在B细胞受到CpG ODN刺激后30分钟内均被诱导,随后1-2小时诱导c-Jun。c-Jun在6小时达到峰值。到40小时,Jun-B和Jun-D占主导地位。含有单个鸟嘌呤三联体/四联体且与富含嘧啶的5'端单元距离适当的合成ODN能够抑制CpG驱动的细胞周期进入和凋亡保护,当它们与刺激型ODN同时添加时,可阻断刺激型ODN诱导的AP-1。刺激30分钟后,添加抑制剂在6小时时不再影响AP-1。没有AP-1亚基能逃脱ODN的抑制。在转染了AP-1-β-半乳糖苷酶报告构建体的细胞系中,抑制性ODN可阻止CpG ODN诱导的AP-1转录活性,但脂多糖(LPS)诱导的AP-1活性不受影响。这些数据表明,抑制性ODN在AP-1诱导近端的位点阻断了CpG ODN驱动的信号通路。

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