Bossers Koen, Meerhoff Gideon, Balesar Rawien, van Dongen Jeroen W, Kruse Chris G, Swaab Dick F, Verhaagen Joost
Laboratory for Neuroregeneration, Netherlands Institute for Neuroscience, Royal Netherlands Academy of Arts and Sciences, Amsterdam, The Netherlands.
Brain Pathol. 2009 Jan;19(1):91-107. doi: 10.1111/j.1750-3639.2008.00171.x. Epub 2008 May 7.
Parkinson's disease (PD) is a neurodegenerative disorder characterized by the progressive loss of dopaminergic neurons in the substantia nigra. We have studied alterations in gene expression in the substantia nigra, the caudate nucleus and putamen of four PD patients and four matched controls using custom designed Agilent microarrays. To gain insight into changes in gene expression during early stages of dopaminergic neurodegeneration, we selectively investigated the relatively spared parts of the PD substantia nigra, and correlated gene expression changes with alterations in neuronal density. We identified changes in the expression of 287 transcripts in the substantia nigra, 16 transcripts in the caudate nucleus and four transcripts in the putamen. For selected transcripts, transcriptional alterations were confirmed with qPCR on a larger set of seven PD cases and seven matched controls. We detected concerted changes in functionally connected groups of genes. In the PD substantia nigra, we observed strong evidence for a reduction in neurotrophic support and alterations in axon guidance cues. As the changes occur in relatively spared parts of the PD substantia nigra, they suggest novel disease mechanisms involving neurotrophic support and axon guidance in early stages of cellular stress events, ultimately leading to dopaminergic cell death in PD.
帕金森病(PD)是一种神经退行性疾病,其特征是黑质中多巴胺能神经元逐渐丧失。我们使用定制设计的安捷伦微阵列研究了4例帕金森病患者和4例匹配对照的黑质、尾状核和壳核中的基因表达变化。为了深入了解多巴胺能神经变性早期阶段的基因表达变化,我们选择性地研究了帕金森病黑质中相对未受影响的部分,并将基因表达变化与神经元密度的改变相关联。我们在黑质中鉴定出287个转录本、在尾状核中鉴定出16个转录本以及在壳核中鉴定出4个转录本的表达变化。对于选定的转录本,在另外一组7例帕金森病病例和7例匹配对照中通过qPCR证实了转录改变。我们检测到功能相关基因组的协同变化。在帕金森病黑质中,我们观察到有力证据表明神经营养支持减少以及轴突导向信号改变。由于这些变化发生在帕金森病黑质中相对未受影响的部分,它们提示了在细胞应激事件早期阶段涉及神经营养支持和轴突导向的新疾病机制,最终导致帕金森病中多巴胺能细胞死亡。