Protein levels of glycogen synthase 3 kinase are normal in progressive supranuclear palsy

被引:5
作者
Borghi, R
Piccini, A
Delacourte, A
Strocchi, P
Zaccheo, D
Tabaton, M
机构
[1] Univ Genoa, Dept Neurosci Ophthalmol & Genet, I-16132 Genoa, Italy
[2] Univ Lille 2, Fac Med, INSERM, U422, F-59045 Lille, France
[3] Univ Bologna, Dept Pharmacol, I-40126 Bologna, Italy
[4] Univ Genoa, Dept Expt Med, Sect Human Anat, I-16132 Genoa, Italy
关键词
progressive supranuclear palsy; GSK3; tau phosphorylation;
D O I
10.1016/j.neulet.2004.05.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Progressive supranuclear palsy (PSP) is a neurodegenerative disorder characterized by pure neurofibrillary tau pathology involving mainly basal ganglia and brain stem nuclei. One of the kinases involved in tau phosphorylation is glycogen synthase 3 kinase (GSK3). In mammals GSK3 is present in two isoforms, alpha and beta regulated by phosphorylation: phosphorylation of Ser-9 in GSK3beta or Ser21 in GSK3alpha leads to inactivation while phosphorylation of Tyr216 in GSK3beta or Tyr279 in GSK3alpha leads to activation. We analyzed the protein levels of GSK3alpha/beta and of the phosphorylated forms GSK3beta S-9, GSK3beta Y-216, GSK3alpha Y-279 in brain tissues of subjects with PSP. The analysis failed to show significant differences of all GSK3 isoforms in PSP in comparison to age-matched control cases. This negative result argues against the role of GSK3 in the pathogenesis of PSP. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:67 / 70
页数:4
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