Impaired regulation of electron transport chain subunit genes by nuclear respiratory factor 2 in multiple sclerosis

被引:47
作者
Pandit, Ashish [1 ]
Vadnal, Jonathan [1 ]
Houston, Sara [1 ]
Freeman, Ernest [1 ]
McDonough, Jennifer [1 ]
机构
[1] Kent State Univ, Sch Biomed Sci, Kent State Oak Clin Consortium MS & Neurodegenera, Kent, OH 44242 USA
关键词
Neurodegeneration; Nuclear respiratory factor 2; Mitochondrial gene expression; N-ACETYL-ASPARTATE; BINDING PROTEIN-ALPHA; CYTOCHROME-C-OXIDASE; MITOCHONDRIAL DYSFUNCTION; DNA-BINDING; AXONAL DAMAGE; RAT-BRAIN; NEURODEGENERATION; ACETYLASPARTATE; DISABILITY;
D O I
10.1016/j.jns.2009.01.009
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Multiple sclerosis (MS) is an inflammatory neurodegenerative disease. Recently, decreased expression of nuclear encoded electron transport chain genes was found in neurons in MS cortex. To understand the transcriptional mechanisms responsible for the coordinate down regulation of these genes, we performed electrophoretic mobility shifts with nuclear extracts isolated from gray matter from nonlesion areas of postmortem MS and control cortex. Nine tissue blocks from eight different MS brains and six matched control blocks from five control brains were analyzed. We identified a decrease in a transcription factor complex containing nuclear respiratory factor-2 (NRF-2) in nuclear extracts isolated from MS cortex. This decrease is Correlated with decreased expression of electron transport chain subunit genes and increased oxidative damage measured by increased anti-nitrotyrosine immunoreactivity. We conclude that in MS Cortex a chronic increase in oxidative stress leads to aberrant regulation of transcription of genes involved in energy metabolism. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:14 / 20
页数:7
相关论文
共 43 条
[1]   Inhibition of N-acetylaspartate production: Implications for H-1 MRS studies in vivo [J].
Bates, TE ;
Strangward, M ;
Keelan, J ;
Davey, GP ;
Munro, PMG ;
Clark, JB .
NEUROREPORT, 1996, 7 (08) :1397-1400
[2]  
BERTRAMS HJ, 1976, J IMMUNOL, V117, P1906
[3]  
Bjartmar C, 2000, ANN NEUROL, V48, P893, DOI 10.1002/1531-8249(200012)48:6<893::AID-ANA10>3.3.CO
[4]  
2-2
[5]   Grey matter pathology in multiple sclerosis [J].
Bö, L ;
Geurts, JJG ;
Mörk, SJ ;
van der Valk, P .
ACTA NEUROLOGICA SCANDINAVICA, 2006, 113 :48-50
[6]   Discordant white matter N-acetylasparate and diffusion MRI measures suggest that chronic metabolic dysfunction contributes to axonal pathology in multiple sclerosis [J].
Cader, S. ;
Johansen-Berg, H. ;
Wylezinska, M. ;
Palace, I. ;
Behrens, T. E. ;
Smith, S. ;
Matthews, P. M. .
NEUROIMAGE, 2007, 36 (01) :19-27
[7]  
CASTLE DJ, 2000, PROTEIN SCI
[8]   Identification of redox-sensitive cysteines in GA binding protein-α that regulate DNA binding and heterodimerization [J].
Chinenov, Y ;
Schmidt, T ;
Yang, XY ;
Martin, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (11) :6203-6209
[9]   N-acetyl aspartate:: A marker for neuronal loss or mitochondrial dysfunction [J].
Clark, JB .
DEVELOPMENTAL NEUROSCIENCE, 1998, 20 (4-5) :271-276
[10]   Relapses and progression of disability in multiple sclerosis. [J].
Confavreux, C ;
Vukusic, S ;
Moreau, T ;
Adeleine, P .
NEW ENGLAND JOURNAL OF MEDICINE, 2000, 343 (20) :1430-1438