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鱼藤酮慢性帕金森病小鼠黑质蛋白质组学研究

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目的:为进一步在蛋白质水平上阐明帕金森病(PD)的发病机制,并寻找与疾病密切相关的疾病特异性蛋白(DSPs),探讨了鱼藤酮诱导的慢性PD小鼠模型脑黑质蛋白质表达谱的改变.方法:采用鱼藤酮制备慢性PD小鼠模型,观察模型小鼠行为学变化,PD模型小鼠黑质区α-突触核蛋白(α-SYN)出现证明模型的成功后行双向电泳实验.Pdques t8.O图形分析软件分析蛋白表达差异信息,用基质辅助激光解吸飞行时间质谱(MALDI-TOF-MS)分析仪进行分析.结果:与对照组相比,实验组α-突触核蛋白,经双向电泳蛋白质组学的研究共有18个蛋白点发生了变化:选其中2个有明显改变的蛋白.结论:新鉴定出1个蛋白,另1个与本课题组前阶段研究的1-甲基4-苯基-1,2,3,6一四氢吡啶(MPTP)模型得出相同的蛋白质.这些蛋白的显著改变可能与PD发病机制密切相关,可作PD的DSPs.
Proteomic research of mouse's substantia nigra of chronic Parkinson's disease induced by rotenone
AIM: To search for the DSPs of PD,we separate and evaluate rotenone-induced differential protein expression through the use of proteomics in the Substantia nigra of a mouse model of chronic Parkinson's disease. METHODS: Establishing Parkinson's mouse model induced by rotenone, proteins of control and treated are extracted, and 2-DE handbook ( Bio-Rad Company ) was refer-enced for two-dimensional electrophoresis. PDQUEST8.0 analytical electrophoresis pattern was adopted to evaluate differential protein expression. The altered protein are identified with MALDI-TOF-MS and database searching. RESULTS: Thirty-two differential protein expressions between the two groups. One is the same result of our study teams, another new protein is evaluated.CONCLUSION:There are two proteins that exhibit differential expression,Coiled-coil domain-containing protein 85A, Ubiquitin-like protein 3 precursor. The changes of these proteins are probably related with the DSPs of PD.

rotenoneParkinson's diseaseproteomicssubstantianigra

龙汉春、张玉平、万金城、陈莹、周长青、彭国光

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重庆医科大学附属第一医院神经内科,重庆400016

鱼藤酮 帕金森病 蛋白质组学 黑质

国家自然科学基金

30370499

2009

第四军医大学学报
第四军医大学

第四军医大学学报

CSTPCDCSCD北大核心
影响因子:0.599
ISSN:1000-2790
年,卷(期):2009.30(23)
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