Kadenbach Bernhard, Ramzan Rabia, Vogt Sebastian
Fachbereich Chemie, Philipps-University, D-35032 Marburg, Germany.
Trends Mol Med. 2009 Apr;15(4):139-47. doi: 10.1016/j.molmed.2009.02.004. Epub 2009 Mar 18.
Aging and degenerative diseases are associated with increased levels of reactive oxygen species (ROS). ROS are mostly produced in mitochondria, and their levels increase with higher mitochondrial membrane potential. Cellular respiratory control is based on inhibition of respiration by high membrane potentials. However, we have described a second mechanism of respiratory control based on allosteric inhibition of cytochrome c oxidase (CcO), the terminal enzyme of the respiratory chain, at high ATP:ADP ratios. The mechanism is independent of membrane potential. We have proposed that feedback inhibition of CcO by ATP keeps the membrane potential and ROS production at low levels. Various forms of stress switch off allosteric ATP-inhibition via reversible dephosphorylation of CcO, resulting in increased membrane potential and cellular ROS levels. This mechanism is proposed to represent a missing molecular link between stress and degenerative diseases.
衰老和退行性疾病与活性氧(ROS)水平升高有关。ROS主要在线粒体中产生,其水平随着线粒体膜电位升高而增加。细胞呼吸控制基于高膜电位对呼吸的抑制作用。然而,我们已经描述了一种基于呼吸链末端酶细胞色素c氧化酶(CcO)在高ATP:ADP比率下的变构抑制的呼吸控制的第二种机制。该机制与膜电位无关。我们提出,ATP对CcO的反馈抑制使膜电位和ROS产生保持在低水平。各种形式的应激通过CcO的可逆去磷酸化关闭变构ATP抑制,导致膜电位和细胞ROS水平升高。该机制被认为是应激与退行性疾病之间缺失的分子联系。