Al Bersaoui Roméo, Robert Isabelle, Lutz Yves, Blanc Frédéric, Sommermeyer-Leroux Ghislaine, Shibaguchi Hirotomo, Aunis Dominique, Fuchs Jean-Paul
Unité 575 INSERM, Physiopathologie du Système Nerveux, Strasbourg, France.
FEBS Lett. 2005 May 9;579(12):2715-21. doi: 10.1016/j.febslet.2005.04.007. Epub 2005 Apr 19.
PrP(c) (cellular prion protein) and Doppel are antagonizing proteins, respectively neuroprotective and neurotoxic. Evidence for Doppel neurotoxicity came from PrP(c)-deficient (Prnp(0/0)) mouse lines developing late onset Purkinje-cell degeneration caused by Doppel overexpression in brain. To address the molecular underpinnings of this cell-type specificity, we generated Doppel N-terminal-specific antibodies and started to examine the spatio-temporal expression of Doppel protein species in Ngsk Prnp(0/0) brain. Although Doppel overexpression is ubiquitous, Western analyses of normal and deglycosylated protein extracts revealed cerebellar patterns distinct from the rest of the brain, supporting the idea that neurotoxicity might be linked to a particular Doppel species pattern. Furthermore, our newly raised antibodies allowed the first Doppel immunohistochemical analyses in brain, showing a distribution in Prnp(0/0) cerebellum similar to PrP(c) in wild type.
细胞朊蛋白(PrP(c))和多普蛋白(Doppel)是相互拮抗的蛋白质,分别具有神经保护和神经毒性作用。多普蛋白具有神经毒性的证据来自于PrP(c)基因缺陷(Prnp(0/0))的小鼠品系,这些小鼠由于大脑中多普蛋白的过度表达而出现迟发性浦肯野细胞变性。为了探究这种细胞类型特异性的分子基础,我们制备了多普蛋白N端特异性抗体,并开始研究多普蛋白在Ngsk Prnp(0/0)小鼠大脑中的时空表达情况。尽管多普蛋白的过度表达是普遍存在的,但对正常和去糖基化蛋白提取物的蛋白质印迹分析显示,小脑的表达模式与大脑其他部位不同,这支持了神经毒性可能与特定的多普蛋白物种模式有关的观点。此外,我们新制备的抗体首次实现了多普蛋白在大脑中的免疫组织化学分析,结果显示其在Prnp(0/0)小鼠小脑的分布与野生型小鼠中PrP(c)的分布相似。