Cha Jang-Ho J
MassGeneral Institute for Neurodegenerative Disease, 114 16th Street/B114-2000, Charlestown, MA 02129-4404, USA.
Prog Neurobiol. 2007 Nov;83(4):228-48. doi: 10.1016/j.pneurobio.2007.03.004. Epub 2007 Apr 1.
While selective neuronal death has been an influential theme in Huntington's disease (HD), there is now a preponderance of evidence that significant neuronal dysfunction precedes frank neuronal death. The best evidence for neuronal dysfunction is the observation that gene expression is altered in HD brain, suggesting that transcriptional dysregulation is a central mechanism. Studies of altered gene expression began with careful observations of postmortem human HD brain and subsequently were accelerated by the development of transgenic mouse models. The application of DNA microarray technology has spurred tremendous progress with respect to the altered transcriptional processes that occur in HD, through gene expression studies of both transgenic mouse models as well as cellular models of HD. Gene expression profiles are remarkably comparable across these models, bolstering the idea that transcriptional signatures reflect an essential feature of disease pathogenesis. Finally, gene expression studies have been applied to human HD, thus not only validating the approach of using model systems, but also solidifying the idea that altered transcription is a key mechanism in HD pathogenesis. In the future, gene expression profiling will be used as a readout in clinical trials aimed at correcting transcriptional dysregulation in Huntington's disease.
虽然选择性神经元死亡一直是亨廷顿舞蹈病(HD)的一个有影响力的主题,但现在有大量证据表明,明显的神经元功能障碍先于明显的神经元死亡。神经元功能障碍的最佳证据是观察到HD大脑中的基因表达发生了改变,这表明转录失调是一种核心机制。对基因表达改变的研究始于对死后人类HD大脑的仔细观察,随后随着转基因小鼠模型的发展而加速。DNA微阵列技术的应用通过对转基因小鼠模型以及HD细胞模型的基因表达研究,在HD中发生的转录过程改变方面取得了巨大进展。这些模型的基因表达谱非常相似,支持了转录特征反映疾病发病机制基本特征的观点。最后,基因表达研究已应用于人类HD,这不仅验证了使用模型系统的方法,也巩固了转录改变是HD发病机制关键机制的观点。未来,基因表达谱将作为旨在纠正亨廷顿舞蹈病转录失调的临床试验中的一个指标。