Src kinases are important regulators of mitochondrial functions

被引:61
作者
Hebert-Chatelain, Etienne [1 ]
机构
[1] Univ Bordeaux, INSERM, U688 Physiopathol Mitochondriale, F-33076 Bordeaux, France
关键词
Mitochondria; Oxidative phosphorylation; Tyrosine phosphorylation; Src kinases; DEPENDENT PROTEIN-KINASE; TYROSINE-PHOSPHORYLATED PROTEINS; NF-KAPPA-B; CYTOCHROME-C; FAMILY KINASES; REVERSIBLE PHOSPHORYLATION; OXIDATIVE-PHOSPHORYLATION; SUCCINATE-DEHYDROGENASE; POSITIVE REGULATOR; INDUCED APOPTOSIS;
D O I
10.1016/j.biocel.2012.08.014
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
Mitochondria produce the most part of the energy used by the cells. This energetic production occurs through the oxidative phosphorylation (OXPHOS) process. Mitochondrial functions such as OXPHOS need to be tightly regulated to respect the needs of cells. Phosphorylation of mitochondrial proteins now appears as a major regulation pathway of mitochondrial functions. Several kinases and phosphatases are specifically targeted to mitochondria where they modulate mitochondrial functions. However, we still poorly understand the extent of tyrosine phosphorylation events on mitochondrial metabolism. Among the tyrosine-kinases observed in mitochondria, Src kinases emerge as key players. In the past years, several mitochondrial proteins were shown to be substrates of Src kinases. Notably, these kinases can impact greatly OXPHOS and apoptosis. Important regulators of Src kinases activity are also observed in mitochondria. The aim of this review is to summarize the recent findings on how overall mitochondrial tyrosine phosphorylation events and more specifically Src kinases can influence mitochondrial functions. The different mechanisms of Src kinases regulation and translocation into mitochondria will be also discussed. This article is part of a Directed Issue entitled: Bioenergetic dysfunction, adaptation and therapy. (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:90 / 98
页数:9
相关论文
共 115 条
[1]   Cyclic AMP Produced inside Mitochondria Regulates Oxidative Phosphorylation [J].
Acin-Perez, Rebeca ;
Salazar, Eric ;
Kamenetsky, Margarita ;
Buck, Jochen ;
Levin, Lonny R. ;
Manfredi, Giovanni .
CELL METABOLISM, 2009, 9 (03) :265-276
[2]   Nitric oxide controls Src kinase activity through a sulfhydryl group modification-mediated Tyr-527-independent and Tyr-416-linked mechanism [J].
Akhand, AK ;
Pu, MY ;
Senga, T ;
Kato, M ;
Suzuki, H ;
Miyata, T ;
Hamaguchi, M ;
Nakashima, I .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (36) :25821-25826
[3]   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
[4]   Identification of tyrosine-phosphorylated proteins of the mitochondrial oxidative phosphorylation machinery [J].
Augereau, O ;
Claverol, S ;
Boudes, N ;
Basurko, MJ ;
Bonneu, M ;
Rossignol, R ;
Mazat, JP ;
Letellier, T ;
Dachary-Prigent, J .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (13) :1478-1488
[5]   Glutaredoxin 2 catalyzes the reversible oxidation and glutathionylation of mitochondrial membrane thiol proteins - Implications for mitochondrial redox regulation and antioxidant defense [J].
Beer, SM ;
Taylor, ER ;
Brown, SE ;
Dahm, CC ;
Costa, NJ ;
Runswick, MJ ;
Murphy, MP .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (46) :47939-47951
[6]   The tyrosine kinase Lck is required for CD95-independent caspase-8 activation and apoptosis in response to ionizing radiation [J].
Belka, C ;
Marini, P ;
Lepple-Wienhues, A ;
Budach, W ;
Jekle, A ;
Los, M ;
Lang, F ;
Schulze-Osthoff, K ;
Gulbins, E ;
Bamberg, M .
ONCOGENE, 1999, 18 (35) :4983-4992
[7]   Phosphorylation of Y845 on the epidermal growth factor receptor mediates binding to the mitochondrial protein cytochrome c oxidase subunit II [J].
Boerner, JL ;
Demory, ML ;
Silva, C ;
Parsons, SJ .
MOLECULAR AND CELLULAR BIOLOGY, 2004, 24 (16) :7059-7071
[8]   Structure and regulation of Src family kinases [J].
Boggon, TJ ;
Eck, MJ .
ONCOGENE, 2004, 23 (48) :7918-7927
[9]   EXPRESSION OF THE V-SRC OR V-FPS ONCOGENE INCREASES FRUCTOSE 2,6-BISPHOSPHATE IN CHICK-EMBRYO FIBROBLASTS - NOVEL MECHANISM FOR THE STIMULATION OF GLYCOLYSIS BY RETROVIRUSES [J].
BOSCA, L ;
MOJENA, M ;
GHYSDAEL, J ;
ROUSSEAU, GG ;
HUE, L .
BIOCHEMICAL JOURNAL, 1986, 236 (02) :595-599
[10]   Regulation, substrates and functions of src [J].
Brown, MT ;
Cooper, JA .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1996, 1287 (2-3) :121-149