Mitochondria - Nucleus communication in neurodegenerative disease. Who talks first, who talks louder?

线粒体 背景(考古学) 细胞生物学 逆行信号 生物 核心 线粒体DNA 细胞器 DNA损伤 细胞适应 细胞室 神经科学 遗传学 细胞 DNA 基因 古生物学
作者
Diana Iulia Savu,Nicoleta Moisoi
出处
期刊:Biochimica Et Biophysica Acta - Bioenergetics [Elsevier]
卷期号:1863 (7): 148588-148588 被引量:1
标识
DOI:10.1016/j.bbabio.2022.148588
摘要

Mitochondria - nuclear coadaptation has been central to eukaryotic evolution. The dynamic dialogue between the two compartments within the context of multiorganellar interactions is critical for maintaining cellular homeostasis and directing the balance survival-death in case of cellular stress. The conceptualisation of mitochondria - nucleus communication has so far been focused on the communication from the mitochondria under stress to the nucleus and the consequent signalling responses, as well as from the nucleus to mitochondria in the context of DNA damage and repair. During ageing processes this dialogue may be better viewed as an integrated bidirectional ‘talk’ with feedback loops that expand beyond these two organelles depending on physiological cues. Here we explore the current views on mitochondria - nucleus dialogue and its role in maintaining cellular health with a focus on brain cells and neurodegenerative disease. Thus, we detail the transcriptional responses initiated by mitochondrial dysfunction in order to protect itself and the general cellular homeostasis. Additionally, we are reviewing the knowledge of the stress pathways initiated by DNA damage which affect mitochondria homeostasis and we add the information provided by the study of combined mitochondrial and genotoxic damage. Finally, we reflect on how each organelle may take the lead in this dialogue in an ageing context where both compartments undergo accumulation of stress and damage and where, perhaps, even the communications' mechanisms may suffer interruptions. • Mitochondrial dysfunction initiates multiple protective signalling mechanisms coordinated at nuclear level. • The cellular response to DNA lesions requires the energetic and metabolic support of the mitochondria. • Mitochondria-nucleus dialogue is an integrated bidirectional ‘talk’ with feedback loops dependent on physiological cues. • The signalling may depend on cell type, subcellular localisation and functional specialization of the mitochondria. • Mitochondria - nucleus bidirectional ‘talk’ occurs in autonomous and non-autonomous manner as well as, transgenerationally.
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