Fan Shaoan, Wu Feng, Martiniuk Frank, Hale Martha L, Ellington Andrew D, Tchou-Wong Kam-Meng
Department of Environmental Medicine, New York University School of Medicine, 57 Old Forge Road, Tuxedo, New York 10987, United States.
World J Gastroenterol. 2008 Nov 7;14(41):6360-5. doi: 10.3748/wjg.14.6360.
To investigate the therapeutic potential of an RNA ligand (aptamer) specific for the catalytic ricin A-chain (RTA), the protective effects of a 31-nucleotide RNA aptamer (31RA), which formed a high affinity complex with RTA, against ricin-induced toxicity in cell-based luciferase translation and cell cytotoxicity assays were evaluated.
To test the therapeutic potential of anti-RTA aptamers in Chinese hamster ovary (CHO) AA8 cells stably transfected with a tetracycline regulatable promoter, ricin ribotoxicity was measured using luciferase and ricin-induced cytotoxicity was ascertained by MTS cell proliferation assay with tetrazolium compound [3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium].
Inhibition of protein synthesis by ricin in CHO AA8 cells resulted in diminished luciferase activity and treatment with polyclonal antibody against deglycosylated RTA (dgA) neutralized the inhibitory effects of ricin on luciferase activity and protected against ricin-induced cytotoxicity as measured by MTS assay. The 31RA anti-RTA aptamer inhibited the translation of luciferase mRNA in cell-free reticulocyte translation assay. 31RA aptamer also partially neutralized the inhibitory effects of ricin on luciferase activity and partially protected against ricin-induced cytotoxicity in CHO AA8 cells.
We have shown that anti-RTA RNA aptamer can protect against ricin ribotoxicity in cell-based luciferase and cell cytotoxicity assays. Hence, RNA aptamer that inhibits RTA enzymatic activity represents a novel class of nucleic acid inhibitor that has the potential to be developed as a therapeutic agent for the treatment of ricin intoxication.
研究针对催化型蓖麻毒蛋白A链(RTA)的RNA配体(适体)的治疗潜力,评估一种与RTA形成高亲和力复合物的31个核苷酸的RNA适体(31RA)在基于细胞的荧光素酶翻译和细胞毒性试验中对蓖麻毒素诱导毒性的保护作用。
为了测试抗RTA适体在中国仓鼠卵巢(CHO)AA8细胞(稳定转染了四环素可调节启动子)中的治疗潜力,使用荧光素酶测量蓖麻毒素的核糖体毒性,并通过用四唑化合物[3-(4,5-二甲基噻唑-2-基)-5-(3-羧基甲氧基苯基)-2-(4-磺基苯基)-2H-四唑]进行的MTS细胞增殖试验确定蓖麻毒素诱导的细胞毒性。
蓖麻毒素对CHO AA8细胞中蛋白质合成的抑制导致荧光素酶活性降低,用抗去糖基化RTA(dgA)的多克隆抗体处理可中和蓖麻毒素对荧光素酶活性的抑制作用,并如MTS试验所测,保护细胞免受蓖麻毒素诱导的细胞毒性。31RA抗RTA适体在无细胞网织红细胞翻译试验中抑制荧光素酶mRNA的翻译。31RA适体还部分中和了蓖麻毒素对CHO AA8细胞中荧光素酶活性的抑制作用,并部分保护细胞免受蓖麻毒素诱导的细胞毒性。
我们已经表明,抗RTA RNA适体在基于细胞的荧光素酶和细胞毒性试验中可保护细胞免受蓖麻毒素的核糖体毒性。因此,抑制RTA酶活性的RNA适体代表了一类新型的核酸抑制剂,有潜力被开发为治疗蓖麻毒素中毒的治疗剂。