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Live by fusion, avoid fission.

机译:通过融合生活,避免裂变。

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Mitochondria are recognized for their role in energy generation but also represent major factors in aging. Over the years, several mito-chondrial processes have been implicated in aging, but their exact role(s) in cellular longevity is often debated.Mitochondria are known to play a prominent role in the induction of apoptosis, a process that significantly contributes to the pathogenesis of age-related diseases. Also, mitochondrial respiration has been connected to aging. According to the free-radical theory of aging, reactive oxygen species (ROS) generated in mitochondria cause mutations in mitochondrial DNA (mtDNA), which lead to increasing defects in respiration and, hence, to a vicious circle of increasing mtDNA damage and ROS. However, controversy remains in this respect, as mutations in mtDNA contribute to aging but are not invariably accompanied by increased ROS.At present, the significance of mitochondrial dynamics in aging is attracting much attention. Mitochondria are very dynamic and continuously change their morphology by fission and fusion events mediated by several GTPases. When fission is affected, extensive mitochondrial networks are formed. Conversely, fusion-deficient cells contain many small organelles. An important current question is why mitochondrial morphology is so important for cell viability.
机译:线粒体因其在能量产生中的作用而被公认,但也代表了衰老的主要因素。多年来,衰老牵涉到许多线粒体过程,但人们对它们在细胞长寿中的确切作用一直存在争议。老年性疾病的发病机理。此外,线粒体呼吸与衰老有关。根据衰老的自由基理论,线粒体中产生的活性氧(ROS)会导致线粒体DNA(mtDNA)发生突变,从而导致呼吸系统缺陷增加,从而导致mtDNA损伤和ROS增加的恶性循环。然而,在这方面仍存在争议,因为mtDNA的突变会导致衰老,但并非总是伴随着ROS的增加。目前,线粒体动力学在衰老中的重要性正引起人们的广泛关注。线粒体是非常动态的,并通过几种GTP酶介导的裂变和融合事件不断改变其形态。当裂变受到影响时,就会形成广泛的线粒体网络。相反,融合缺陷细胞含有许多小细胞器。当前的一个重要问题是,为什么线粒体形态对于细胞活力如此重要。

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