Modulation of mitochondrial protein phosphorylation by soluble adenylyl cyclase ameliorates cytochrome oxidase defects

被引:94
作者
Acin-Perez, Rebeca [1 ]
Salazar, Eric [2 ,3 ]
Brosel, Sonja [4 ]
Yang, Hua [4 ]
Schon, Eric A. [4 ]
Manfredi, Giovanni [1 ]
机构
[1] Cornell Univ, Weill Med Coll, Dept Neurol & Neurosci, New York, NY 10021 USA
[2] Cornell Univ, Weill Med Coll, Triinst MD PhD Program, New York, NY 10021 USA
[3] Cornell Univ, Weill Med Coll, Dept Pharmacol, New York, NY 10021 USA
[4] Cornell Univ, Dept Neurol, New York, NY 10021 USA
关键词
mitochondria; sAC; cytochrome oxidase; mtDNA; ROS; CAMP-DEPENDENT PHOSPHORYLATION; BOVINE HEART-MITOCHONDRIA; STOP-CODON MUTATION; C-OXIDASE; OXIDATIVE-PHOSPHORYLATION; COMPLEX-I; SUBUNIT-I; TYROSINE PHOSPHORYLATION; SKELETAL-MUSCLE; CULTURED-CELLS;
D O I
10.1002/emmm.200900046
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Phosphorylation of respiratory chain components has emerged as a mode of regulation of mitochondrial energy metabolism, but its mechanisms are still largely unexplored. A recently discovered intramitochondrial signalling pathway links CO2 generated by the Krebs cycle with the respiratory chain, through the action of a mitochondrial soluble adenylyl cyclase (mt-sAC). Cytochrome oxidase (COX), whose deficiency causes a number of fatal metabolic disorders, is a key mitochondrial enzyme activated by mt-sAC. We have now discovered that the mt-sAC pathway modulates mitochondrial biogenesis in a reactive oxygen species dependent manner, in cultured cells and in animals with COX deficiency. We show that upregulation of mt-sAC normalizes ROS production and mitochondrial biogenesis, thereby restoring mitochondrial function. This is the first example of manipulation of a mitochondrial signalling pathway to achieve a direct positive modulation of COX, with clear implications for the development of novel approaches to treat mitochondrial diseases.
引用
收藏
页码:392 / 406
页数:15
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