Arima H, Takahashi M, Aramaki Y, Sakamoto T, Tsuchiya S
School of Pharmacy, Tokyo University of Pharmacy and Life Science, Japan.
Antisense Nucleic Acid Drug Dev. 1998 Aug;8(4):319-27. doi: 10.1089/oli.1.1998.8.319.
The effects of phosphorothioate antisense oligonucleotides (AS-S-oligos) directed against murine interleukin-10 (IL-10) mRNA on IL-10 production in RAW264.7 cells, a murine macrophage-like cell line, when stimulated by lipopolysaccharide (LPS) were examined. Of the six AS-S-oligos used, AS-S-oligos directed against the 3'-untranslated region (3'-UTR) of IL-10 mRNA (AS6-S-oligo) showed the strongest inhibitory effect on IL-10 production, and this inhibition was dose and time dependent. Reverse transcription-polymerase chain reaction (RT-PCR) revealed that the antisense effect originated from a specific reduction of target IL-10 mRNA by hybridization with AS6-S-oligo. In addition, AS6-S-oligo did not affect tumor necrosis factor-alpha (TNF-alpha) production in cells stimulated by LPS, and S-oligos with control sequences did not affect IL-10 production. These findings suggested that AS6-S-oligo most powerfully inhibited IL-10 production in macrophages by an antisense mechanism.
研究了针对小鼠白细胞介素10(IL-10)mRNA的硫代磷酸反义寡核苷酸(AS-S-寡核苷酸)对小鼠巨噬细胞样细胞系RAW264.7细胞在脂多糖(LPS)刺激下IL-10产生的影响。在所使用的六种AS-S-寡核苷酸中,针对IL-10 mRNA 3'-非翻译区(3'-UTR)的AS-S-寡核苷酸(AS6-S-寡核苷酸)对IL-10产生表现出最强的抑制作用,且这种抑制呈剂量和时间依赖性。逆转录-聚合酶链反应(RT-PCR)显示,反义效应源于与AS6-S-寡核苷酸杂交导致靶IL-10 mRNA特异性减少。此外,AS6-S-寡核苷酸不影响LPS刺激的细胞中肿瘤坏死因子-α(TNF-α)的产生,具有对照序列的S-寡核苷酸也不影响IL-10的产生。这些发现表明,AS6-S-寡核苷酸通过反义机制最有力地抑制巨噬细胞中IL-10的产生。