Individual dopaminergic neurons show raised iron levels in Parkinson disease

被引:263
作者
Oakley, A. E.
Collingwood, J. F.
Dobson, J.
Love, G.
Perrott, H. R.
Edwardson, J. A.
Elstner, M.
Morris, C. M.
机构
[1] Univ Newcastle, Med Toxicol Res Ctr, Wolfson Unit Clin Pharmacol, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
[2] Univ Newcastle, Inst Ageing & Hlth, Wolfson Unit Clin Pharmacol, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
[3] Univ Newcastle, Dept Neurol, Newcastle Upon Tyne NE2 4AA, Tyne & Wear, England
[4] Univ Keele, Postgrad Med Sch, Inst Sci & Technol Med, Keele ST5 5BG, Staffs, England
[5] Univ Bath, Ctr Electron Opt Studies, Bath BA2 7AY, Avon, England
[6] Univ Munich, Dept Neurol, D-8000 Munich, Germany
基金
英国工程与自然科学研究理事会;
关键词
D O I
10.1212/01.wnl.0000262033.01945.9a
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: Evidence suggests that abnormal iron metabolism is associated with Parkinson disease (PD), with raised iron levels found in pathologically affected areas in PD. It is unknown if this elevated iron is actually associated with neurons or reactive glia, and we therefore addressed this issue by determining if raised iron was present in single dopaminergic neurons. Methods: We used unfixed frozen sections from postmortem tissue of PD patients and elderly normal individuals to avoid metal contamination and translocation. Levels of iron and other elements were measured using sensitive and specific wavelength dispersive electron probe x-ray microanalysis coupled with cathodoluminescence spectroscopy in individual substantia nigra dopaminergic neurons. Results: We identified raised intraneuronal iron in single defined substantia nigra neurons in PD ( mean neuronal iron 2,838 vs 1,611, p < 0.0001) but not in other movement disorders such as Huntington disease. These findings were unrelated to the density of remaining neurons. Conclusions: Primary changes in neuronal iron could lead to neurodegeneration in Parkinson disease.
引用
收藏
页码:1820 / 1825
页数:6
相关论文
共 37 条
[1]   A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe [J].
Abbas, N ;
Lücking, CB ;
Ricard, S ;
Dürr, A ;
Bonifati, V ;
De Michele, G ;
Bouley, S ;
Vaughan, JR ;
Gasser, T ;
Marconi, R ;
Broussolle, E ;
Brefel-Courbon, C ;
Harhangi, BS ;
Oostra, AB ;
Fabrizio, E ;
Böhme, GA ;
Pradier, L ;
Wood, NW ;
Filla, A ;
Meco, G ;
Denefle, P ;
Agid, Y ;
Brice, A .
HUMAN MOLECULAR GENETICS, 1999, 8 (04) :567-574
[2]   T2 RELAXATION-TIME IN PATIENTS WITH PARKINSONS-DISEASE [J].
ANTONINI, A ;
LEENDERS, KL ;
MEIER, D ;
OERTEL, WH ;
BOESIGER, P ;
ANLIKER, M .
NEUROLOGY, 1993, 43 (04) :697-700
[3]   High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease [J].
Bender, A ;
Krishnan, KJ ;
Morris, CM ;
Taylor, GA ;
Reeve, AK ;
Perry, RH ;
Jaros, E ;
Hersheson, JS ;
Betts, J ;
Klopstock, T ;
Taylor, RW ;
Turnbull, DM .
NATURE GENETICS, 2006, 38 (05) :515-517
[4]  
Collingwood JF, 2005, J ALZHEIMERS DIS, V7, P267
[5]   ISOFORMS OF FERRITIN HAVE A SPECIFIC CELLULAR-DISTRIBUTION IN THE BRAIN [J].
CONNOR, JR ;
BOESHORE, KL ;
BENKOVIC, SA ;
MENZIES, SL .
JOURNAL OF NEUROSCIENCE RESEARCH, 1994, 37 (04) :461-465
[6]   Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease [J].
Curtis, ARJ ;
Fey, C ;
Morris, CM ;
Bindoff, LA ;
Ince, PG ;
Chinnery, PF ;
Coulthard, A ;
Jackson, MJ ;
Jackson, AP ;
McHale, DP ;
Hay, D ;
Barker, WA ;
Markham, AF ;
Bates, D ;
Curtis, A ;
Burn, J .
NATURE GENETICS, 2001, 28 (04) :350-354
[7]  
El-Agnaf OMA, 2002, BIOCHEM SOC T, V30, P559
[8]   Mossbauer spectroscopy and ELISA studies reveal differences between. Parkinson's disease and control substantia nigra [J].
Galazka-Friedman, J ;
Bauminger, ER ;
Koziorowski, D ;
Friedman, A .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2004, 1688 (02) :130-136
[9]  
Gerlach M, 1997, MOVEMENT DISORD, V12, P258
[10]   ANATOMY, PIGMENTATION, VENTRAL AND DORSAL SUBPOPULATIONS OF THE SUBSTANTIA-NIGRA, AND DIFFERENTIAL CELL-DEATH IN PARKINSONS-DISEASE [J].
GIBB, WRG ;
LEES, AJ .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1991, 54 (05) :388-396