Livigni Alessandra, Scorziello Antonella, Agnese Savina, Adornetto Annagrazia, Carlucci Annalisa, Garbi Corrado, Castaldo Imma, Annunziato Lucio, Avvedimento Enrico V, Feliciello Antonio
Dipartimento di Biologia e Patologia Molecolare e Cellulare, Istituto di Endocrinologia ed Oncologia Sperimentale, CNR, 80131 Napoli, Italy.
Mol Biol Cell. 2006 Jan;17(1):263-71. doi: 10.1091/mbc.e05-09-0827. Epub 2005 Oct 26.
AKAP121 focuses distinct signaling events from membrane to mitochondria by binding and targeting cAMP-dependent protein kinase (PKA), protein tyrosine phosphatase (PTPD1), and mRNA. We find that AKAP121 also targets src tyrosine kinase to mitochondria via PTPD1. AKAP121 increased src-dependent phosphorylation of mitochondrial substrates and enhanced the activity of cytochrome c oxidase, a component of the mitochondrial respiratory chain. Mitochondrial membrane potential and ATP oxidative synthesis were enhanced by AKAP121 in an src- and PKA-dependent manner. Finally, siRNA-mediated silencing of endogenous AKAP121 drastically impaired synthesis and accumulation of mitochondrial ATP. These findings indicate that AKAP121, through its role in enhancing cAMP and tyrosine kinase signaling to distal organelles, is an important regulator in mitochondrial metabolism.
AKAP121通过结合并靶向环磷酸腺苷依赖性蛋白激酶(PKA)、蛋白酪氨酸磷酸酶(PTPD1)和信使核糖核酸,将不同的信号事件从细胞膜聚焦到线粒体。我们发现,AKAP121还通过PTPD1将src酪氨酸激酶靶向线粒体。AKAP121增加了src依赖的线粒体底物磷酸化,并增强了细胞色素c氧化酶(线粒体呼吸链的一个组成部分)的活性。AKAP121以src和PKA依赖的方式增强线粒体膜电位和ATP氧化合成。最后,小干扰RNA介导的内源性AKAP121沉默极大地损害了线粒体ATP的合成和积累。这些发现表明,AKAP121通过其在增强向远端细胞器的环磷酸腺苷和酪氨酸激酶信号传导中的作用,是线粒体代谢的重要调节因子。