Mitochondrial signalling and homeostasis: from cell biology to neurological disease

被引:76
作者
Collier, Jack J. [1 ]
Olahova, Monika [2 ]
McWilliams, Thomas G. [3 ,4 ]
Taylor, Robert W. [2 ,5 ]
机构
[1] McGill Univ, Montreal Neurol Inst, Dept Neurol & Neurosurg, Montreal, PQ, Canada
[2] Newcastle Univ, Translat & Clin Res Inst, Wellcome Ctr Mitochondrial Res, Newcastle Upon Tyne, Tyne & Wear, England
[3] Univ Helsinki, Translat Stem Cell Biol & Metab Program, Res Programs Unit, Helsinki, Finland
[4] Univ Helsinki, Fac Med, Dept Anat, Helsinki, Finland
[5] Newcastle Univ, NHS Highly Specialised Serv Rare Mitochondrial Di, Newcastle Upon Tyne, Tyne & Wear, England
基金
英国医学研究理事会; 芬兰科学院;
关键词
HUNTINGTON-DISEASE; CA2+ DYNAMICS; MOUSE MODEL; VESICLES; PROMOTES; PATHWAY; PEROXISOMES; MUTATIONS; TRANSPORT; ORGANELLE;
D O I
10.1016/j.tins.2022.12.001
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Efforts to understand how mitochondrial dysfunction contributes to neurode-generation have primarily focussed on the role of mitochondria in neuronal energy metabolism. However, progress in understanding the etiological nature of emerging mitochondrial functions has yielded new ideas about the mitochondrial basis of neurological disease. Studies aimed at deciphering how mitochondria signal through interorganellar contacts, vesicular trafficking, and metabolic transmission have revealed that mitochondrial regulation of immunometabolism, cell death, organelle dynamics, and neuroimmune interplay are critical determinants of neural health. Moreover, the homeostatic mechanisms that exist to protect mitochondrial health through turnover via nanoscale proteostasis and lysosomal degradation have become integrated within mitochondrial signalling pathways to support meta-bolic plasticity and stress responses in the nervous system. This review highlights how these distinct mitochondrial pathways converge to influence neurological health and contribute to disease pathology.
引用
收藏
页码:137 / 152
页数:16
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