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Retinoids inhibit measles virus in vitro via nuclear retinoid receptor signaling pathways.

机译:类维生素A通过核类维生素A受体信号传导途径在体外抑制麻疹病毒。

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Measles virus (MV) infects 30 million children every year, resulting in more than half a million deaths. Vitamin A (retinol) treatment of acute measles can reduce measles-associated mortality by 50-80%. We sought to determine whether or not retinoids can act directly to limit MV output from infected cells. Physiologic concentrations of retinol were found to inhibit MV output in PBMC and a range of cell lines of epithelial and endothelial origin (40-50%). Near complete inhibition of viral output was achieved in some cells/lines treated with all-trans retinoic acid (ATRA) and 9-cis RA (9cRA). Important attenuation of the anti-MV effect of retinoids in R4 cells, a subclone of a retinoid-responsive cell line (NB4) deficient in RAR signaling, demonstrates that this effect is mediated at least in part by nuclear retinoid receptor signaling pathways. Inhibition of MV replication could not be fully explained as a result of retinoid effects on cell differentiation, proliferation or viability, particularly at low retinoid concentrations (1-10nM). These data provide the first evidence that retinoids can directly inhibit MV in vitro, and raise the possibility that retinoids may have similar actions in vivo.
机译:麻疹病毒(MV)每年感染3000万儿童,导致超过半百万人死亡。维生素A(视黄醇)治疗急性麻疹可使麻疹相关死亡率降低50-80%。我们试图确定类维生素A是否可以直接发挥作用,以限制感染细胞的MV输出。发现视黄醇的生理浓度会抑制PBMC和一系列上皮和内皮来源的细胞系中的MV输出(40-50%)。在用全反式视黄酸(ATRA)和9-顺式RA(9cRA)处理的某些细胞/株中,病毒输出几乎完全被抑制。在RAR信号缺乏的类维生素A反应性细胞系(NB4)的亚克隆R4细胞中,类维生素A的抗MV效应的重要衰减表明,这种作用至少部分地由核类维生素A受体信号通路介导。由于类视色素对细胞分化,增殖或活力的影响,尤其是在低类视色素浓度(1-10nM)下,无法完全解释MV复制的抑制作用。这些数据提供了类维生素A可以在体外直接抑制MV的第一个证据,并增加了类维生素A在体内可能具有类似作用的可能性。

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