Functional impact of PTP1B-mediated Src regulation on oxidative phosphorylation in rat brain mitochondria

被引:29
作者
Chatelain, Etienne Hebert [1 ]
Dupuy, Jean-William [2 ]
Letellier, Thierry [1 ]
Dachary-Prigent, Jeanne [1 ]
机构
[1] Univ Bordeaux 2, INSERM U688, F-33076 Bordeaux, France
[2] Univ Bordeaux, Ctr Genom Fonct, F-33076 Bordeaux, France
基金
加拿大自然科学与工程研究理事会;
关键词
Src kinase; PTP1B; Mitochondria; Oxidative phosphorylation; Regulation; Signaling; Respiration; CYTOCHROME-C-OXIDASE; TYROSINE PHOSPHATASE-ACTIVITY; IN-VIVO; KINASE-ACTIVITY; IDENTIFICATION; SPECIFICITY; MODULATION; PROTEINS; MUTATION; CULTURES;
D O I
10.1007/s00018-010-0573-6
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
Given the presence of Src and PTP1B within rat brain mitochondria, we have investigated whether PTP1B regulates Src activity in mitochondria as in the cytosol. Results showed that Src was stimulated by in vitro addition of ATP to mitochondria, and this stimulation was reversed by a membrane-permeable allosteric inhibitor of PTP1B and by a potent selective Src inhibitor. They also indicated a direct action of PTP1B on phosphorylated tyrosine 527 residue of Src, thus implicating a role for PTP1B in the modulation of Src activity in mitochondria. Putative Src and PTP1B substrates were identified by liquid chromatography tandem mass spectrometry and two-dimensional blue native/SDS-PAGE. Both inhibitors inhibited ADP-stimulated respirations concurrently with Src activation and complex IV activation by ATP, while having no effect or increasing the activity of the other complexes. Our analysis emphasizes the regulatory function of Src and its modulation by PTP1B on oxidative phosphorylation in mitochondria.
引用
收藏
页码:2603 / 2613
页数:11
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