Center for Virus Research, Westmead Millennium Institute, Westmead Hospital, The University of Sydney, Westmead, NSW 2145, Sydney, Australia.
Mol Neurodegener. 2010 Jun 24;5:27. doi: 10.1186/1750-1326-5-27.
The pathogenesis of HIV-associated dementia (HAD) is poorly understood. To date, detailed proteomic fingerprinting directly from autopsied brain tissues of HAD and HIV non-dementia patients has not been performed.
Here, we have analyzed total proteins from the frontal cortex of 9 HAD and 5 HIV non-dementia patients. Using 2-Dimensional differential in-gel electrophoresis (2-DIGE) to analyze the brain tissue proteome, 76 differentially expressed proteins (p < 0.05; fold change>1.25) were identified between HAD and HIV non-dementia patients, of which 36 protein spots (based on 3D appearance of spots on the images) were chosen for the mass spectrometry analysis. The large majority of identified proteins were represented in the energy metabolic (mitochondria) and signal transduction pathways. Furthermore, over 90% of the protein candidates are common to both HAD and other non-viral neurodegenerative disease, such as Alzheimer's disease. The data was further validated using specific antibodies to 4 proteins (CA2, GS, CKMT and CRMP2) by western blot (WB) in the same samples used for 2D-DIGE, with additional confirmation by immunohistochemitsry (IHC) using frontal lobe tissue from different HAD and HIV+ non-dementia patients. The validation for all 4 antibodies by WB and IHC was in concordance with the DIGE results, lending further credence to the current findings.
These results suggest not only convergent pathogenetic pathways for the two diseases but also the possibility of increased Alzheimer's disease (AD) susceptibility in HAD patients whose life expectancy has been significantly increased by highly active antiretroviral therapy.
HIV 相关痴呆(HAD)的发病机制尚不清楚。迄今为止,尚未对 HAD 和 HIV 非痴呆患者的尸检脑组织进行直接的详细蛋白质组指纹图谱分析。
在这里,我们分析了 9 例 HAD 和 5 例 HIV 非痴呆患者额叶皮层的总蛋白。使用二维差异凝胶电泳(2-DIGE)分析脑组织蛋白质组,在 HAD 和 HIV 非痴呆患者之间鉴定出 76 种差异表达蛋白(p < 0.05;倍数变化>1.25),其中 36 个蛋白斑点(基于斑点在图像上的 3D 外观)被选择进行质谱分析。鉴定出的大多数蛋白质代表能量代谢(线粒体)和信号转导途径。此外,超过 90%的候选蛋白与 HAD 和其他非病毒性神经退行性疾病(如阿尔茨海默病)共同存在。使用针对 4 种蛋白质(CA2、GS、CKMT 和 CRMP2)的特异性抗体通过 Western blot(WB)对相同样本进行进一步验证,对来自不同 HAD 和 HIV+非痴呆患者的额叶组织进行免疫组织化学(IHC)验证,结果与 2D-DIGE 一致。所有 4 种抗体的 WB 和 IHC 验证均与 DIGE 结果一致,进一步证实了目前的发现。
这些结果不仅表明两种疾病存在趋同的发病途径,而且还表明在通过高效抗逆转录病毒疗法显著延长预期寿命的 HAD 患者中,阿尔茨海默病(AD)的易感性增加的可能性。