Regulation of mitochondrial functions by protein phosphorylation and dephosphorylation

被引:79
作者
Lim, Sangbin [1 ]
Smith, Kelly R. [1 ]
Lim, Ssang-Taek Steve [2 ]
Tian, Rong [3 ]
Lu, Jianrong [4 ]
Tan, Ming [1 ]
机构
[1] Univ S Alabama, Ctr Cell Death & Metab, Mitchell Canc Inst, Mobile, AL 36688 USA
[2] Univ S Alabama, Coll Med, Dept Biochem & Mol Biol, Mobile, AL USA
[3] Univ Washington, Mitochondria & Metab Ctr, Dept Anesthesiol & Pain Med, Seattle, WA 98195 USA
[4] Univ Florida, Coll Med, Dept Biochem & Mol Biol, Gainesville, FL 32610 USA
基金
美国国家卫生研究院;
关键词
Mitochondria; Kinase; Phosphatase; Phosphorylation; Metabolism; GLYCOGEN-SYNTHASE KINASE-3-BETA; KINASE-C-DELTA; CHRONIC MYELOGENOUS LEUKEMIA; PYRUVATE-DEHYDROGENASE ACTIVITY; AMYLOID-BETA-PEPTIDE; ABL TYROSINE KINASE; FACTOR-KAPPA-B; PARKINSONS-DISEASE; PKC-EPSILON; PINK1; FUNCTION;
D O I
10.1186/s13578-016-0089-3
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
The mitochondria are double membrane-bound organelles found in most eukaryotic cells. They generate most of the cell's energy supply of adenosine triphosphate (ATP). Protein phosphorylation and dephosphorylation are critical mechanisms in the regulation of cell signaling networks and are essential for almost all the cellular functions. For many decades, mitochondria were considered autonomous organelles merely functioning to generate energy for cells to survive and proliferate, and were thought to be independent of the cellular signaling networks. Consequently, phosphorylation and dephosphorylation processes of mitochondrial kinases and phosphatases were largely neglected. However, evidence accumulated in recent years on mitochondria-localized kinases/phosphatases has changed this longstanding view. Mitochondria are increasingly recognized as a hub for cell signaling, and many kinases and phosphatases have been reported to localize in mitochondria and play important functions. However, the strength of the evidence on mitochondrial localization and the activities of the reported kinases and phosphatases vary greatly, and the detailed mechanisms on how these kinases/phosphatases translocate to mitochondria, their subsequent function, and the physiological and pathological implications of their localization are still poorly understood. Here, we provide an updated perspective on the recent advancement in this area, with an emphasis on the implications of mitochondrial kinases/phosphatases in cancer and several other diseases.
引用
收藏
页数:15
相关论文
共 176 条
[1]   ROS-Triggered Phosphorylation of Complex II by Fgr Kinase Regulates Cellular Adaptation to Fuel Use [J].
Acin-Perez, Rebeca ;
Carrascoso, Isabel ;
Baixauli, Francesc ;
Roche-Molina, Marta ;
Latorre-Pellicer, Ana ;
Fernandez-Silva, Patricio ;
Mittelbrunn, Maria ;
Sanchez-Madrid, Francisco ;
Perez-Martos, Acisclo ;
Lowell, Clifford A. ;
Manfredi, Giovanni ;
Antonio Enriquez, Jose .
CELL METABOLISM, 2014, 19 (06) :1020-1033
[2]   Essential role of A-kinase anchor protein 121 for cAMP signaling to mitochondria [J].
Affaitati, A ;
Cardone, L ;
de Cristofaro, T ;
Carlucci, A ;
Ginsberg, MD ;
Varrone, S ;
Gottesman, ME ;
Avvedimento, EV ;
Feliciello, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (06) :4286-4294
[3]   Activation of the neuronal c-Abl tyrosine kinase by amyloid-β-peptide and reactive oxygen species [J].
Alvarez, AR ;
Sandoval, PC ;
Leal, NR ;
Castro, PU ;
Kosik, KS .
NEUROBIOLOGY OF DISEASE, 2004, 17 (02) :326-336
[4]   Localization of PTP-1B, SHP-2, and Src exclusively in rat brain mitochondria and functional consequences [J].
Arachiche, Amal ;
Augereau, Olivier ;
Decossas, Marion ;
Pertuiset, Claire ;
Gontier, Etienne ;
Letellier, Thierry ;
Dachary-Prigent, Jeanne .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2008, 283 (36) :24406-24411
[5]   Mitochondrial PKCε and MAPK form signaling modules in the murine heart -: Enhanced mitochondrial PKCε-MAPK interactions and differential MAPK activation in PKCε-induced cardioprotection [J].
Baines, CP ;
Zhang, J ;
Wang, GW ;
Zheng, YT ;
Xiu, JX ;
Cardwell, EM ;
Bolli, R ;
Ping, P .
CIRCULATION RESEARCH, 2002, 90 (04) :390-397
[6]   Acute adenosine preconditioning is mediated by p38 MAPK activation in discrete subcellular compartments [J].
Ballard-Croft, C ;
Kristo, G ;
Yoshimura, Y ;
Reid, E ;
Keith, BJ ;
Mentzer, RM ;
Lasley, RD .
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY, 2005, 288 (03) :H1359-H1366
[7]   The basal flux of Akt in the mitochondria is mediated by heat shock protein 90 [J].
Barksdale, Keri A. ;
Bijur, Gautam N. .
JOURNAL OF NEUROCHEMISTRY, 2009, 108 (05) :1289-1299
[8]   The small heat shock-related protein, HSP20, is phosphorylated on serine 16 during cyclic nucleotide-dependent relaxation [J].
Beall, A ;
Bagwell, D ;
Woodrum, D ;
Stoming, TA ;
Kato, K ;
Suzuki, A ;
Rasmussen, H ;
Brophy, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (16) :11344-11351
[9]   THE CHRONIC MYELOGENOUS LEUKEMIA SPECIFIC P210-PROTEIN IS THE PRODUCT OF THE BCR/ABL HYBRID GENE [J].
BEN-NERIAH, Y ;
DALEY, GQ ;
MESMASSON, AM ;
WITTE, ON ;
BALTIMORE, D .
SCIENCE, 1986, 233 (4760) :212-214
[10]  
Bhakar AL, 2003, J NEUROSCI, V23, P11373