细胞胺诱导的神经毒性的机制
Jia-Cheng Liu1, Dongpeng Wang1,2, Elsa Callen1
1Laboratory of Genome Integrity, National Cancer Institute, NIH, Bethesda, MD, USA.
通过干扰DNA脱甲基化和修复而导致神经元中的DNA损伤. 这解释了某些癌症药物的神经毒性.
科学领域:
- 表观遗传学
- 神经科学
- DNA 修复
背景情况:
- 甲基化后神经元具有高水平的甲基化细胞素和5-甲基细胞素.
- 这些DNA表观遗传修饰的功能意义在很大程度上仍未知.
研究的目的:
- 研究神经元中的DNA表观遗传修饰的功能相关性.
- 阐明细胞类药物的神经毒性背后的机制.
主要方法:
- 在TET中介脱甲基化过程中由细胞氨基酸诱导的DNA双链断裂.
- 分析了TDG依赖的基切除修复和DNA结合酶IV在细胞因子诱导损伤中的作用.
- 在Purkinje和Golgi细胞中检查了体内神经毒性.
- 评估了由gemcitabine引起的DNA损伤及其通过DNA结合酶III的修复.
主要成果:
- 通过在TET中介脱甲基化过程中中断TDG依赖的基体切除修复,诱导神经元中的DNA双链断裂.
- 这些断裂被DNA连接酶IV转化为缺失和转位.
- 普尔金耶和戈尔吉细胞特别容易受到细胞氨基酸诱导的DNA损伤,影响运动协调至关重要的基因.
- 杰姆西塔会导致单链断裂,由DNA连接酶III进行修复,从而降低毒性.
结论:
- 建立了TET介导的DNA脱甲基化,基因切除修复和神经元中的基因表达之间的机制联系.
- 提供了不同的神经毒性特征的科学理由.
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