Activation of the unfolded protein response in Parkinson's disease

被引:421
作者
Hoozemans, J. J. M.
van Haastert, E. S.
Eikelenboom, P.
de Vos, R. A. I.
Rozemuller, J. M.
Scheper, W.
机构
[1] Vrije Univ Amsterdam, Ctr Med, Dept Pathol, NL-1081 HV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Ctr Med, Dept Psychiat, NL-1081 HV Amsterdam, Netherlands
[3] Lab Neuropathol E Netherlands, Enschede, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Neurogenet Lab, NL-1105 AZ Amsterdam, Netherlands
[5] Univ Amsterdam, Acad Med Ctr, Dept Neurol, NL-1105 AZ Amsterdam, Netherlands
关键词
Parkinson's disease; unfolded protein response; endoplasmic reticulum stress; PERK; alpha-synuclein; eIF2; alpha;
D O I
10.1016/j.bbrc.2007.01.043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Parkinson's disease (PD) is, at the neuropathological level, characterized by the accumulation of misfolded proteins. The presence of misfolded proteins can trigger a cellular stress response in the endoplasmic reticulum (ER) called the Unfolded Protein Response (UPR). The UPR has been shown to be involved in cellular models for PD. In this study, we investigated UPR activation in the substantia nigra of control and PD patients. Immunoreactivity for the UPR activation markers phosphorylated pancreatic ER kinase (pPERK) and phosphorylated eukaryotic initiation factor 2 alpha (peIF2 alpha) is detected in neuromelanin containing dopaminergic neurons in the substantia nigra of PD cases but not in control cases. In addition, pPERK immunoreactivity is colocalized with increased alpha-synuclein immunoreactivity in dopaminergic neurons. These data show that the UPR is activated in PD and that UPR activation is closely associated with the accumulation and aggregation of alpha-synuclein. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:707 / 711
页数:5
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