Suppr超能文献

带有5'-CG-3'基序的六聚体回文寡核苷酸可诱导干扰素的产生。

Hexamer palindromic oligonucleotides with 5'-CG-3' motif(s) induce production of interferon.

作者信息

Sonehara K, Saito H, Kuramoto E, Yamamoto S, Yamamoto T, Tokunaga T

机构信息

Institute of Biological Science, Mitsui Pharmaceuticals, Inc., Chiba, Japan.

出版信息

J Interferon Cytokine Res. 1996 Oct;16(10):799-803. doi: 10.1089/jir.1996.16.799.

Abstract

We have shown previously that 30-mer oligonucleotides containing hexamer palindromic sequences with 5'-CG-3' motif(s) induce interferon (IFN), activate natural killer (NK) cells, and thus exhibit tumor-regressing activity. The present study showed that a hexamer palindromic oligonucleotide (5'-AACGTT-3') alone induced IFN from mouse spleen cells when added with cationic liposomes. Accordingly, 32 kinds of hexamer palindromic oligonucleotides were tested for their ability to induce IFN in the presence of cationic liposomes. The results show that oligonucleotides with NACGTN and NTCGAN sequences exhibited the strongest activity. ACGCGT and TCGCGA also possessed moderate but significant activity. In contrast, palindromes without CG motif(s) were devoid of the activity. No hexamer oligonucleotides showed the activity when liposomes were absent. A complete palindromic sequence was essential as any single base substitution resulted in diminished activity. Among variety of palindromic oligonucleotides of different sizes with an ACGT sequence at the center, the tetramer oligonucleotide was without activity, whereas the activity of hexamer and longer oligonucleotides was almost equally high. These results strongly suggest that the minimal essential structure required for IFN induction is the hexamer palindromic sequence with CG motif(s).

摘要

我们之前已经表明,含有带有5'-CG-3'基序的六聚体回文序列的30聚体寡核苷酸可诱导干扰素(IFN),激活自然杀伤(NK)细胞,从而展现出肿瘤消退活性。本研究表明,单独的六聚体回文寡核苷酸(5'-AACGTT-3')与阳离子脂质体一起添加时可从小鼠脾细胞诱导出IFN。因此,测试了32种六聚体回文寡核苷酸在阳离子脂质体存在下诱导IFN的能力。结果显示,具有NACGTN和NTCGAN序列的寡核苷酸表现出最强的活性。ACGCGT和TCGCGA也具有中等但显著的活性。相比之下,没有CG基序的回文序列则没有这种活性。当不存在脂质体时,没有六聚体寡核苷酸显示出活性。完整的回文序列至关重要,因为任何单个碱基替换都会导致活性降低。在各种不同大小且中心具有ACGT序列的回文寡核苷酸中,四聚体寡核苷酸没有活性,而六聚体及更长的寡核苷酸的活性几乎同样高。这些结果强烈表明,诱导IFN所需的最小基本结构是带有CG基序的六聚体回文序列。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验