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5-氟尿嘧啶通过破坏青春期小鼠的TCF7L2/HDAC1/HDAC2复合物导致严重的中枢神经系统脱髓鞘。

5-Fluorouracil causes severe CNS demyelination by disruption of TCF7L2/HDAC1/HDAC2 complex in adolescent mice.

作者信息

Weng Qinjie, Tan Biqin, Wang Jiajia, Wang Jing, Zhou Hui, Shi Jing, He QiaoJun, Yang Bo

机构信息

Institute of Pharmacology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China; Center for Drug Safety Evaluation and Research, Zhejiang University, Hangzhou 310058, China.

Institute of Pharmacology, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.

出版信息

Toxicology. 2014 Nov 5;325:144-50. doi: 10.1016/j.tox.2014.08.011. Epub 2014 Aug 29.

Abstract

Several studies have showed the anti-cancer efficacy of 5-FU (5-fluorouracil) on pediatric tumors. Although the delayed demyelination induced by 5-FU in adult patients has been reported, the effect of 5-FU on oligodendrocyte myelination in adolescence is still unknown. Here, we demonstrate that systemic administration with 5-FU leads to immediate demyelination in the central nervous system (CNS) of adolescent mice, which is mainly attributed to the death of OLs. Gene-chip microarray transcriptome analysis identifies that oligodendrocyte-specific factor TCF7L2 may be a toxic target of 5-FU-impaired myelination. 5-FU-decreased TCF7L2 results in disruption of the interaction between TCF7L2 and HDAC1/2. Inhibition of crucial myelination-promoting factors by 5-FU is more significantly antagonized by co-transfection of TCF7L2, HDAC1 and HDAC2 than TCF7L2 alone. Our findings reveal that 5-FU could acutely induce the severe myelin degeneration in adolescence and disruption of TCF7L2/HDAC1/HDAC2 complex is at least partially involved in 5-FU-induced demyelination.

摘要

多项研究表明5-氟尿嘧啶(5-FU)对小儿肿瘤具有抗癌疗效。尽管已有报道称5-FU在成年患者中会引发迟发性脱髓鞘,但5-FU对青少年少突胶质细胞髓鞘形成的影响仍不清楚。在此,我们证明对青春期小鼠进行5-FU全身给药会导致中枢神经系统(CNS)立即发生脱髓鞘,这主要归因于少突胶质细胞(OLs)的死亡。基因芯片微阵列转录组分析确定少突胶质细胞特异性因子TCF7L2可能是5-FU损害髓鞘形成的毒性靶点。5-FU使TCF7L2减少,导致TCF7L2与HDAC1/2之间的相互作用中断。与单独转染TCF7L2相比,共转染TCF7L2、HDAC1和HDAC2能更显著地拮抗5-FU对关键髓鞘形成促进因子的抑制作用。我们的研究结果表明,5-FU可在青春期急性诱导严重的髓鞘变性,并且TCF7L2/HDAC1/HDAC2复合物的破坏至少部分参与了5-FU诱导的脱髓鞘过程。

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