Fernandez-Abascal Jesus, Artal-Sanz Marta
Andalusian Centre for Developmental Biology (CABD), CSIC-Universidad Pablo de Olavide-Junta de Andalucía, Sevilla, Spain.
Department of Molecular Biology and Biochemical Engineering, Universidad Pablo de Olavide, Seville, Spain.
Front Aging. 2022 Nov 3;3:1043300. doi: 10.3389/fragi.2022.1043300. eCollection 2022.
The incidence of age-related neurodegenerative disorders has risen with the increase of life expectancy. Unfortunately, the diagnosis of such disorders is in most cases only possible when the neurodegeneration status is already advanced, and symptoms are evident. Although age-related neurodegeneration is a common phenomenon in living animals, the cellular and molecular mechanisms behind remain poorly understood. Pathways leading to neurodegeneration usually diverge from a common starting point, mitochondrial stress, which can serve as a potential target for early diagnosis and treatments. Interestingly, the evolutionarily conserved mitochondrial prohibitin (PHB) complex is a key regulator of ageing and metabolism that has been associated with neurodegenerative diseases. However, its role in neurodegeneration is still not well characterized. The PHB complex shows protective or toxic effects in different genetic and physiological contexts, while mitochondrial and cellular stress promote both up and downregulation of PHB expression. With this review we aim to shed light into the complex world of PHB's function in neurodegeneration by putting together the latest advances in neurodegeneration and mitochondrial homeostasis associated with PHB. A better understanding of the role of PHB in neurodegeneration will add knowledge to neuron deterioration during ageing and help to identify early molecular markers of mitochondrial stress. This review will deepen our understanding of age-related neurodegeneration and provide questions to be addressed, relevant to human health and to improve the life quality of the elderly.
随着预期寿命的增加,与年龄相关的神经退行性疾病的发病率也在上升。不幸的是,在大多数情况下,只有当神经退行性变状态已经进展且症状明显时,才能诊断出此类疾病。尽管与年龄相关的神经退行性变是活体动物中的常见现象,但其背后的细胞和分子机制仍知之甚少。导致神经退行性变的途径通常从一个共同的起点——线粒体应激—— diverge 开来,线粒体应激可作为早期诊断和治疗的潜在靶点。有趣的是,进化上保守的线粒体抑制素(PHB)复合体是衰老和代谢的关键调节因子,与神经退行性疾病有关。然而,其在神经退行性变中的作用仍未得到充分表征。PHB复合体在不同的遗传和生理背景下表现出保护或毒性作用,而线粒体和细胞应激则促进PHB表达的上调和下调。通过这篇综述,我们旨在通过整合与PHB相关的神经退行性变和线粒体稳态的最新进展,阐明PHB在神经退行性变中的复杂功能世界。更好地理解PHB在神经退行性变中的作用将增加对衰老过程中神经元退化的认识,并有助于识别线粒体应激的早期分子标志物。这篇综述将加深我们对与年龄相关的神经退行性变的理解,并提出与人类健康相关的有待解决的问题,以提高老年人的生活质量。 (注:原文中“diverge”此处翻译较难准确对应一个简洁中文词,保留英文更合适,若一定要翻译可译为“分歧、偏离等”,这里暂保留英文)