Department of Cell and Developmental Biology and Consortium for Mitochondrial Research, UCL, Gower Street, London WC1E 6BT, UK.
Department of Cell and Developmental Biology and Consortium for Mitochondrial Research, UCL, Gower Street, London WC1E 6BT, UK.
Trends Cell Biol. 2022 May;32(5):391-405. doi: 10.1016/j.tcb.2021.10.005. Epub 2021 Nov 23.
Mitochondria generate the energy to sustain cell viability and serve as a hub for cell signalling. Their own genome (mtDNA) encodes genes critical for oxidative phosphorylation. Mutations of mtDNA cause major disease and disability with a wide range of presentations and severity. We review here an emerging body of data suggesting that changes in cell metabolism and signalling pathways in response to the presence of mtDNA mutations play a key role in shaping disease presentation and progression. Understanding the impact of mtDNA mutations on cellular energy homeostasis and signalling pathways seems fundamental to identify novel therapeutic interventions with the potential to improve the prognosis for patients with primary mitochondrial disease.
线粒体产生维持细胞活力所需的能量,并作为细胞信号的枢纽。它们自身的基因组(mtDNA)编码对氧化磷酸化至关重要的基因。mtDNA 的突变会导致多种表现形式和严重程度的重大疾病和残疾。我们在这里回顾了一系列新的数据,这些数据表明,细胞代谢和信号通路的变化对 mtDNA 突变的存在的反应在塑造疾病表现和进展方面起着关键作用。了解 mtDNA 突变对细胞能量平衡和信号通路的影响似乎对于确定具有改善原发性线粒体疾病患者预后潜力的新的治疗干预措施至关重要。