Mitochondrial nuclear receptors and transcription factors: Who's minding the cell?

被引:37
作者
Lee, Junghee [1 ,2 ]
Sharma, Swati [1 ,2 ]
Kim, Jinho [1 ,2 ]
Ferrante, Robert J. [1 ,3 ]
Ryu, Hoon [1 ,2 ]
机构
[1] Boston Univ, Sch Med,VA Med Ctr, Dept Neurol, GRECC Unit 182B, Bedford, MA 01730 USA
[2] Vet Affairs Med Ctr, Ctr Geriatr Res Educ & Clin, Bedford, MA USA
[3] Boston Univ, Sch Med, Dept Pathol & Psychiat, Boston, MA 02215 USA
关键词
mitochondria; neurodegeneration; transcription regulation;
D O I
10.1002/jnr.21564
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Mitochondria are power organelles generating biochemical energy, ATP, in the cell. Mitochondria play a variety of roles, including integrating extracellular signals and executing critical intracellular events, such as neuronal cell survival and death. Increasing evidence suggests that a cross-talk mechanism between mitochondria and the nucleus is closely related to neuronal function and activity. Nuclear receptors (estrogen receptors, thyroid (T3) hormone receptor, peroxisome proliferators-activated receptor gamma2) and transcription factors (cAMP response binding protein, p53) have been found to target mitochondria and exert pro-survival and prodeath pathways. In this context, the regulation of mitochondrial function via the translocation of nuclear receptors and transcription factors may underlie some of the mechanisms involved in neuronal survival and death. Understanding the function of nuclear receptors and transcription factors in the mitochondria may provide important pharmacological utility in the treatment of neurodegenerative conditions. Thus, the modulation of signaling pathways via mitochondria-targeting nuclear receptors and transcription factors is rapidly emerging as a novel therapeutic target. (C) 2007 Wiley-Liss, Inc.
引用
收藏
页码:961 / 971
页数:11
相关论文
共 98 条
[1]  
Albers DS, 2000, J NEURAL TRANSM-SUPP, P133
[2]   p53 mediates cellular dysfunction and behavioral abnormalities in Huntington's disease [J].
Bae, BI ;
Xu, H ;
Igarashi, S ;
Fujimuro, M ;
Agrawal, N ;
Taya, Y ;
Hayward, SD ;
Moran, TH ;
Montell, C ;
Ross, CA ;
Snyder, SH ;
Sawa, A .
NEURON, 2005, 47 (01) :29-41
[3]   DO DEFECTS IN MITOCHONDRIAL ENERGY-METABOLISM UNDERLIE THE PATHOLOGY OF NEURODEGENERATIVE DISEASES [J].
BEAL, MF ;
HYMAN, BT ;
KOROSHETZ, W .
TRENDS IN NEUROSCIENCES, 1993, 16 (04) :125-131
[4]   Experience-dependent increase in cAMP-responsive element binding protein in synaptic and nonsynaptic mitochondria of the rat hippocampus [J].
Bevilaqua, LRM ;
Cammarota, M ;
Paratcha, G ;
de Stein, ML ;
Izquierdo, I ;
Medina, JH .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1999, 11 (10) :3753-3756
[5]  
Bogdanov MB, 1998, J NEUROCHEM, V71, P2642
[6]   A dynamic machinery for import of mitochondrial precursor proteins [J].
Bohnert, Maria ;
Pfanner, Nikolaus ;
van der Laan, Martin .
FEBS LETTERS, 2007, 581 (15) :2802-2810
[7]   P53-DEPENDENT APOPTOSIS IN THE ABSENCE OF TRANSCRIPTIONAL ACTIVATION OF P53-TARGET GENES [J].
CAELLES, C ;
HELMBERG, A ;
KARIN, M .
NATURE, 1994, 370 (6486) :220-223
[8]  
CANIMAROTA M, 1999, J NEUROCHEM, V72, P2272
[9]   A 45 kDa protein related to PPARγ2, induced by peroxisome proliferators, is located in the mitochondrial matrix [J].
Casas, F ;
Domenjoud, L ;
Rochard, P ;
Hatier, R ;
Rodier, A ;
Daury, L ;
Bianchi, A ;
Kremarik-Bouillaud, P ;
Becuwe, P ;
Keller, JM ;
Schohn, H ;
Wrutniak-Cabello, C ;
Cabello, G ;
Dauça, M .
FEBS LETTERS, 2000, 478 (1-2) :4-8
[10]   Mitochondrial localization of ERα and ERβ in human MCF7 cells [J].
Chen, JQ ;
Delannoy, M ;
Cooke, C ;
Yager, JD .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2004, 286 (06) :E1011-E1022