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
[81]   THYROID-HORMONE ACTION - MITOCHONDRIAL PATHWAY [J].
STERLING, K ;
MILCH, PO ;
BRENNER, MA ;
LAZARUS, JH .
SCIENCE, 1977, 197 (4307) :996-999
[82]   17β-estradiol promotes striatal medium size spiny neuronal maturation in vitro [J].
Stroppolo, A ;
Tian, C ;
Guinea, B ;
Olm, V ;
Sheffield, R ;
Sommer, J ;
Ehrlich, ME .
NEUROENDOCRINOLOGY, 2004, 79 (05) :259-267
[83]   The mitochondrial genome: structure, transcription, translation and replication [J].
Taanman, JW .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1999, 1410 (02) :103-123
[84]   P53 stabilization is decreased upon NFκB activation:: A role for NFκB in acquisition of resistance to chemotherapy [J].
Tergaonkar, V ;
Pando, M ;
Vafa, O ;
Wahl, G ;
Verma, I .
CANCER CELL, 2002, 1 (05) :493-503
[85]   WT p53, but not tumor-derived mutants, bind to Bcl2 via the DNA binding domain and induce mitochondrial permeabilization [J].
Tomita, Y ;
Marchenko, N ;
Erster, S ;
Nemajerova, A ;
Dehner, A ;
Klein, C ;
Pan, HG ;
Kessler, H ;
Pancoska, P ;
Moll, UM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (13) :8600-8606
[86]   A CONSERVED HEPTAMER MOTIF FOR RIBOSOMAL-RNA TRANSCRIPTION TERMINATION IN ANIMAL MITOCHONDRIA [J].
VALVERDE, JR ;
MARCO, R ;
GARESSE, R .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (12) :5368-5371
[87]   Mitochondrial diseases in man and mouse [J].
Wallace, DC .
SCIENCE, 1999, 283 (5407) :1482-1488
[88]   17 beta-estradiol protects against NMDA-induced excitotoxicity by direct inhibition of NMDA receptors [J].
Weaver, CE ;
ParkChung, M ;
Gibbs, TT ;
Farb, DH .
BRAIN RESEARCH, 1997, 761 (02) :338-341
[89]  
Wilson BE, 1996, MOL CELL BIOL, V16, P5546
[90]   REQUIREMENT FOR THE ORPHAN STEROID-RECEPTOR NUR77 IN APOPTOSIS OF T-CELL HYBRIDOMAS [J].
WORONICZ, JD ;
CALNAN, B ;
NGO, V ;
WINOTO, A .
NATURE, 1994, 367 (6460) :277-281