Laboratory of Stem Cell Biology and Pharmacology of Neurodegenerative Diseases, Department of Biosciences, University of Milan, 20122 Milan, Italy.
Istituto Nazionale Genetica Molecolare, Romeo ed Enrica Invernizzi, Milan 20122, Italy.
Proc Natl Acad Sci U S A. 2018 Jan 23;115(4):E762-E771. doi: 10.1073/pnas.1715865115. Epub 2018 Jan 8.
Increasing evidence suggests that early neurodevelopmental defects in Huntington's disease (HD) patients could contribute to the later adult neurodegenerative phenotype. Here, by using HD-derived induced pluripotent stem cell lines, we report that early telencephalic induction and late neural identity are affected in cortical and striatal populations. We show that a large CAG expansion causes complete failure of the neuro-ectodermal acquisition, while cells carrying shorter CAGs repeats show gross abnormalities in neural rosette formation as well as disrupted cytoarchitecture in cortical organoids. Gene-expression analysis showed that control organoid overlapped with mature human fetal cortical areas, while HD organoids correlated with the immature ventricular zone/subventricular zone. We also report that defects in neuroectoderm and rosette formation could be rescued by molecular and pharmacological approaches leading to a recovery of striatal identity. These results show that mutant huntingtin precludes normal neuronal fate acquisition and highlights a possible connection between mutant huntingtin and abnormal neural development in HD.
越来越多的证据表明,亨廷顿病(HD)患者的早期神经发育缺陷可能导致后期成人神经退行性表型。在这里,我们使用源自 HD 的诱导多能干细胞系报告称,皮质和纹状体群体中的早期端脑诱导和晚期神经身份受到影响。我们表明,较大的 CAG 扩展导致神经外胚层的完全获得失败,而携带较短 CAG 重复的细胞在神经玫瑰花结形成中存在严重异常,并且在皮质类器官中细胞结构被破坏。基因表达分析表明,对照类器官与成熟的人类胎儿皮质区域重叠,而 HD 类器官与未成熟的脑室区/室下区相关。我们还报告说,通过分子和药理学方法可以挽救神经外胚层和玫瑰花结形成的缺陷,从而恢复纹状体的特征。这些结果表明,突变亨廷顿蛋白阻止了正常神经元命运的获得,并强调了突变亨廷顿蛋白与 HD 中异常神经发育之间可能存在联系。