Heaven Michael R, Flint Daniel, Randall Shan M, Sosunov Alexander A, Wilson Landon, Barnes Stephen, Goldman James E, Muddiman David C, Brenner Michael
Keck Fourier Transform Mass Spectrometry Laboratory, Department of Chemistry, North Carolina State University , Raleigh, North Carolina 27695, United States.
J Proteome Res. 2016 Jul 1;15(7):2265-82. doi: 10.1021/acs.jproteome.6b00316. Epub 2016 Jun 2.
Alexander disease (AxD) is a neurodegenerative disorder characterized by astrocytic protein aggregates called Rosenthal fibers (RFs). We used mouse models of AxD to determine the protein composition of RFs to obtain information about disease mechanisms including the hypothesis that sequestration of proteins in RFs contributes to disease. A method was developed for RF enrichment, and analysis of the resulting fraction using isobaric tags for relative and absolute quantitation mass spectrometry identified 77 proteins not previously associated with RFs. Three of five proteins selected for follow-up were confirmed enriched in the RF fraction by immunobloting of both the AxD mouse models and human patients: receptor for activated protein C kinase 1 (RACK1), G1/S-specific cyclin D2, and ATP-dependent RNA helicase DDX3X. Immunohistochemistry validated cyclin D2 as a new RF component, but results for RACK1 and DDX3X were equivocal. None of these was decreased in the non-RF fractions compared to controls. A similar result was obtained for the previously known RF component, alphaB-crystallin, which had been a candidate for sequestration. Thus, no support was obtained for the sequestration hypothesis for AxD. Providing possible insight into disease progression, the association of several of the RF proteins with stress granules suggests a role for stress granules in the origin of RFs.
亚历山大病(AxD)是一种神经退行性疾病,其特征是存在被称为罗森塔尔纤维(RFs)的星形胶质细胞蛋白聚集体。我们利用AxD小鼠模型来确定RFs的蛋白质组成,以获取有关疾病机制的信息,包括RFs中蛋白质的隔离导致疾病的假说。我们开发了一种RF富集方法,使用等压标签相对和绝对定量质谱法对所得组分进行分析,鉴定出77种先前未与RFs相关的蛋白质。通过对AxD小鼠模型和人类患者进行免疫印迹,选定用于后续研究的5种蛋白质中有3种被证实在RF组分中富集:活化蛋白C激酶1受体(RACK1)、G1/S特异性细胞周期蛋白D2和ATP依赖性RNA解旋酶DDX3X。免疫组织化学验证细胞周期蛋白D2是一种新的RF成分,但RACK1和DDX3X的结果不明确。与对照组相比,这些蛋白质在非RF组分中均未减少。对于先前已知的RF成分αB晶状体蛋白,也得到了类似的结果,它曾是隔离的候选蛋白。因此,未获得支持AxD隔离假说的证据。几种RF蛋白与应激颗粒的关联为疾病进展提供了可能的见解,表明应激颗粒在RFs起源中起作用。