Liu Yingjun, Zhou Qinbo, Tang Mi, Fu Ning, Shao Wei, Zhang Shuzhen, Yin Yanqing, Zeng Rong, Wang Xiaomin, Hu Gang, Zhou Jiawei
Institute of Neuroscience, State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China.
Institute of Neuroscience, State Key Laboratory of Neuroscience, CAS Center for Excellence in Brain Science, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai, China; Jiangsu Key Laboratory of Neurodegeneration, Department of Pharmacology, Nanjing Medical University, Nanjing, Jiangsu, China.
Neurobiol Aging. 2015 Apr;36(4):1686-1691. doi: 10.1016/j.neurobiolaging.2015.01.015. Epub 2015 Jan 22.
Parkinson's disease (PD) is one of the most devastating neurodegenerative disorders. The underlying mechanisms of the characteristic neurodegeneration in the substantia nigra (SN) are still not fully understood. To better understand the molecular events occurring in the SN of PD brain, we used the culture-derived isotope tag-based quantitative proteomics to compare the protein expression profiles in the nigral tissue of PD patients and control subjects. We identified a total of 11 differentially expressed proteins, including alphaB-crystallin (Cryab). Both the levels and pattern of Cryab expression in the SN were validated. It was revealed that Cryab was markedly upregulated in the SN of PD brain. Cryab expression was also upregulated in reactive astrocytes and microglia in a neurotoxin-induced mouse PD model. Moreover, we showed increased expression of Cryab in cytoplasmic inclusions in a subset of glial cells in Parkinsonian brain. Thus, we identified Cryab that is highly expressed in the SN of PD brain and may be involved in the glial pathology during dopaminergic neuron degeneration in PD.
帕金森病(PD)是最具破坏性的神经退行性疾病之一。黑质(SN)中特征性神经退行性变的潜在机制仍未完全明确。为了更好地理解PD患者大脑黑质中发生的分子事件,我们使用基于培养物衍生同位素标记的定量蛋白质组学方法,比较了PD患者和对照受试者黑质组织中的蛋白质表达谱。我们共鉴定出11种差异表达蛋白,其中包括αB-晶状体蛋白(Cryab)。黑质中Cryab表达的水平和模式均得到了验证。结果显示,PD患者大脑黑质中Cryab显著上调。在神经毒素诱导的小鼠PD模型中,反应性星形胶质细胞和小胶质细胞中Cryab表达也上调。此外,我们发现帕金森病大脑中一部分胶质细胞的胞质内含物中Cryab表达增加。因此,我们鉴定出在PD患者大脑黑质中高表达且可能参与PD多巴胺能神经元变性过程中胶质病理改变的Cryab。