突变的亨廷丁对PGC-1alpha的转录抑制导致线粒体功能障碍和神经退行
Libin Cui1, Hyunkyung Jeong, Fran Borovecki
1Department of Neurology, Massachusetts General Hospital, Harvard Medical School, MassGeneral Institute for Neurodegeneration, Charlestown, MA 02129 USA.
Cell
|October 5, 2006
概括
亨廷顿病涉及由于突变的亨廷丁抑制PGC-1alpha.alpha的线粒体功能受损. 恢复PGC-1alpha可以提供神经保护,并在亨廷顿病模型中逆转毒性影响.
科学领域:
- 神经退行性疾病的神经退行性疾病
- 线粒体生物学 线粒体生物学
- 基因调节 基因调节
背景情况:
- 亨廷顿病 (HD) 是一种遗传性神经退行性疾病.
- 病原发生涉及转录性放松调节和改变能量代谢.
- 突变的亨廷丁蛋白质是病因.
研究的目的:
- 为了研究PGC-1alpha在亨廷顿病的发病过程中的作用.
- 确定PGC-1alpha是否可以抵消突变狩猎的影响.
主要方法:
- 研究了突变的亨廷丁对PGC-1α基因转录的影响.
- 使用了PGC-1alpha淘汰和HD淘汰的小鼠模型.
- 在培养的条状神经元和体内使用lentiviral交付评估神经保护.
主要成果:
- 突变的亨廷丁通过干扰CREB/TAF4通路来抑制PGC-1α转录.
- 在HD小鼠中,PGC-1α缺乏会加剧神经退行和运动缺陷.
- 在体外,PGC-1α表达部分逆转了突变的亨廷丁毒性,并在体内提供神经保护.
结论:
- PGC-1α在早期的HD中对能量代谢的调节起着至关重要的作用.
- 准PGC-1alpha代表了亨廷顿病的潜在治疗策略.
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