Deng Shengchang, Zhou Ying, Ouyang Dong, Xiong Junping, Zhang Lei, Tu Changchun, Zhang Keping, Song Zengliang, Zhang Fanglin
School of Medicine, Nanchang University, Nanchang, Jiangxi 330006, P.R. China.
Jiangxi Police College, Nanchang, Jiangxi 330103, P.R. China.
Biomed Rep. 2014 Jan;2(1):137-141. doi: 10.3892/br.2013.194. Epub 2013 Nov 1.
Importin α (Imα) plays an important role during the shuttling of the HIV-1 preintegration complex (PIC) from the cytoplasm to the nucleus. Imα may bind to the glucocorticoid receptor (GR), which is localized to nucleus following hormone binding. However, it remains unclear whether the binding of dexamethasone (Dex) to GR affects the Imα redistribution and, thus, alters PIC import. In our study, 293T cells were transfected with the lentiviral vector (LV) carrying the luciferase (Luci) gene following Dex or RU486 pretreatment. The Luci activity (LucA) in the Dex or RU486 group was significantly higher compared to that in the control group (P≤0.01). The effects of Dex and RU486 were inhibited by the Imα inhibitor Bimax1 (P≤0.01), although the inhibitory effect of Bimax1 was alleviated by increasing the Dex dose. Furthermore, it was observed that the LucA in the 30-min Dex treatment group was lower compared to that in the 30-min Dex pretreatment group (P≤0.01). These results suggested that Dex may improve PIC import via increasing the cytoplasmic Imα levels. Kunming mice were transfected with the LV, either 30 min or 15 h following an intraperitoneal injection of Dex. The LucA in the liver of the 30-min group mice was significantly lower compared to that of the 15-h group mice (P≤0.01), suggesting that the effect of Dex on LV infection depends mainly on the suppression of immune and inflammatory responses . Taken together, our data indicated that the effect of Dex on LV infection may be associated with Imα, constituting a novel signaling pathway mediating the effects of Dex on HIV-1 infection.
输入蛋白α(Imα)在HIV-1整合前复合物(PIC)从细胞质穿梭至细胞核的过程中发挥着重要作用。Imα可能与糖皮质激素受体(GR)结合,后者在激素结合后定位于细胞核。然而,地塞米松(Dex)与GR的结合是否会影响Imα的重新分布,进而改变PIC的导入,目前尚不清楚。在我们的研究中,用携带荧光素酶(Luci)基因的慢病毒载体(LV)转染293T细胞,转染前进行Dex或RU486预处理。与对照组相比,Dex或RU486组的荧光素酶活性(LucA)显著更高(P≤0.01)。Imα抑制剂Bimax1可抑制Dex和RU486的作用(P≤0.01),尽管增加Dex剂量可减轻Bimax1的抑制作用。此外,观察到30分钟Dex处理组的LucA低于30分钟Dex预处理组(P≤0.01)。这些结果表明,Dex可能通过增加细胞质中Imα的水平来改善PIC的导入。昆明小鼠在腹腔注射Dex后30分钟或15小时用LV转染。30分钟组小鼠肝脏中的LucA显著低于15小时组小鼠(P≤0.01),表明Dex对LV感染的影响主要取决于对免疫和炎症反应的抑制。综上所述,我们的数据表明Dex对LV感染的影响可能与Imα有关,构成了一条介导Dex对HIV-1感染作用的新信号通路。