Laboratory of Experimental Biophysics, Centre for Advanced Technologies, Tashkent 100174, Uzbekistan.
Cell Physiology and Pathology Laboratory, Orel State University, 302026 Orel, Russia.
Cells. 2022 Feb 17;11(4):706. doi: 10.3390/cells11040706.
Neurodegenerative disorders are currently incurable devastating diseases which are characterized by the slow and progressive loss of neurons in specific brain regions. Progress in the investigation of the mechanisms of these disorders helped to identify a number of genes associated with familial forms of these diseases and a number of toxins and risk factors which trigger sporadic and toxic forms of these diseases. Recently, some similarities in the mechanisms of neurodegenerative diseases were identified, including the involvement of mitochondria, oxidative stress, and the abnormality of Ca signaling in neurons and astrocytes. Thus, mitochondria produce reactive oxygen species during metabolism which play a further role in redox signaling, but this may also act as an additional trigger for abnormal mitochondrial calcium handling, resulting in mitochondrial calcium overload. Combinations of these factors can be the trigger of neuronal cell death in some pathologies. Here, we review the latest literature on the crosstalk of reactive oxygen species and Ca in brain mitochondria in physiology and beyond, considering how changes in mitochondrial metabolism or redox signaling can convert this interaction into a pathological event.
神经退行性疾病是目前无法治愈的破坏性疾病,其特征是特定脑区神经元的缓慢进行性丧失。对这些疾病机制的研究进展有助于确定与这些疾病的家族形式相关的一些基因,以及一些毒素和风险因素,这些因素会引发这些疾病的散发性和毒性形式。最近,在神经退行性疾病的机制中发现了一些相似之处,包括线粒体的参与、氧化应激以及神经元和星形胶质细胞中 Ca 信号的异常。因此,线粒体在代谢过程中产生活性氧,在氧化还原信号中发挥进一步的作用,但这也可能作为异常线粒体钙处理的额外触发因素,导致线粒体钙超载。这些因素的组合可能是某些病理学中神经元细胞死亡的触发因素。在这里,我们回顾了关于脑线粒体中活性氧和 Ca 相互作用的最新文献,考虑了线粒体代谢或氧化还原信号的变化如何将这种相互作用转化为病理事件。