Department of Pediatrics, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, Shaanxi 710004, P.R. China.
Mol Med Rep. 2018 Jan;17(1):1198-1204. doi: 10.3892/mmr.2017.7939. Epub 2017 Nov 2.
To understand multidrug resistance gene expression in reactive astrocytes, the present study involved stimulated astrocytes with tumor necrosis factor (TNF)‑α and determined gene expression by reverse transcription‑quantitative polymerase chain reaction and western blot analysis. Stimulation induced P‑glycoprotein (gp) and multidrug resistance‑associated protein (MRP0) 1 expression, which peaked by 24 h. Interestingly, the expression of P‑gp and Mrp1 correlated with cell proliferation. Therefore, reactivation of astrocytes may increase P‑gp and Mrp1 expression through TNF‑α and nuclear factor (NF)‑κB signaling. To the best of the authors' knowledge, the present study is the first to demonstrate that in vitro activated astrocytes likely induced P‑gp and Mrp1 expression by increasing NF‑κB expression. The results of the present study provide a novel insight into the mechanism of refractory epilepsy and suggest inhibiting cytokine signaling may block multidrug resistance.
为了研究反应性星形胶质细胞中多药耐药基因的表达,本研究用肿瘤坏死因子(TNF)-α刺激星形胶质细胞,并通过逆转录-定量聚合酶链反应和 Western blot 分析来确定基因表达。刺激诱导 P-糖蛋白(gp)和多药耐药相关蛋白(MRP0)1 的表达,在 24 小时达到峰值。有趣的是,P-gp 和 Mrp1 的表达与细胞增殖相关。因此,星形胶质细胞的再激活可能通过 TNF-α和核因子(NF)-κB 信号增加 P-gp 和 Mrp1 的表达。据作者所知,本研究首次表明,体外激活的星形胶质细胞可能通过增加 NF-κB 的表达来诱导 P-gp 和 Mrp1 的表达。本研究的结果为耐药性癫痫的发病机制提供了新的见解,并提示抑制细胞因子信号可能阻断多药耐药。