Bowles Kathryn R, Brooks Simon P, Dunnett Stephen B, Jones Lesley
Institute of Psychological Medicine and Clinical Neurosciences, MRC centre for Neuropsychiatric Genetics and Genomics, School of Medicine, Hadyn Ellis building, Maindy Road, Cardiff University, Cardiff CF24 4HQ, Wales, United Kingdom.
The Brain Repair Group, School of Biosciences, Cardiff University, Museum Avenue, Cardiff CF10 3AX, Wales, United Kingdom.
PLoS One. 2015 Dec 14;10(12):e0144864. doi: 10.1371/journal.pone.0144864. eCollection 2015.
Huntington's disease is a neurodegenerative disorder characterised primarily by motor abnormalities, and is caused by an expanded polyglutamine repeat in the huntingtin protein. Huntingtin dynamically shuttles between subcellular compartments, and the mutant huntingtin protein is mislocalised to cell nuclei, where it may interfere with nuclear functions, such as transcription. However, the mechanism by which mislocalisation of mutant huntingtin occurs is currently unknown. An immortalised embryonic striatal cell model of HD (StHdhQ111) was stimulated with epidermal growth factor in order to determine whether the subcellular localisation of huntingtin is dependent on kinase signalling pathway activation. Aberrant phosphorylation of AKT and MEK signalling pathways was identified in cells carrying mutant huntingtin. Activity within these pathways was found to contribute to the regulation of huntingtin and mutant huntingtin localisation, as well as to the expression of immediate-early genes. We propose that altered kinase signalling is a phenotype of Huntington's disease that occurs prior to cell death; specifically, that altered kinase signalling may influence huntingtin localisation, which in turn may impact upon nuclear processes such as transcriptional regulation. Aiming to restore the balance of activity between kinase signalling networks may therefore prove to be an effective approach to delaying Huntington's disease symptom development and progression.
亨廷顿舞蹈症是一种主要以运动异常为特征的神经退行性疾病,由亨廷顿蛋白中多聚谷氨酰胺重复序列扩增所致。亨廷顿蛋白在亚细胞区室间动态穿梭,而突变的亨廷顿蛋白会错误定位于细胞核,在那里它可能干扰核功能,如转录。然而,突变的亨廷顿蛋白错误定位发生的机制目前尚不清楚。为了确定亨廷顿蛋白的亚细胞定位是否依赖于激酶信号通路激活,用表皮生长因子刺激了一种永生化的亨廷顿舞蹈症胚胎纹状体细胞模型(StHdhQ111)。在携带突变亨廷顿蛋白的细胞中发现了AKT和MEK信号通路的异常磷酸化。发现这些通路中的活性有助于调节亨廷顿蛋白和突变亨廷顿蛋白的定位,以及即刻早期基因的表达。我们提出,激酶信号改变是亨廷顿舞蹈症在细胞死亡之前出现的一种表型;具体而言,激酶信号改变可能影响亨廷顿蛋白的定位,这反过来可能影响诸如转录调控等核过程。因此,旨在恢复激酶信号网络之间活性平衡可能被证明是延缓亨廷顿舞蹈症症状发展和进展的一种有效方法。