Weng Qinjie, Tan Biqin, Wang Jiajia, Wang Jing, Zhou Hui, Shi Jing, He QiaoJun, Yang Bo
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.
Toxicology. 2014 Nov 5;325:144-50. doi: 10.1016/j.tox.2014.08.011. Epub 2014 Aug 29.
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.
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。