Faculty of Medicine & Dentistry, Neuroscience and Mental Health Institute, University of Alberta, Edmonton, Canada.
Wellcome Trust- MRC Cambridge Stem Cell Institute, University of Cambridge, Cambridge, UK.
Mol Neurodegener. 2022 May 7;17(1):34. doi: 10.1186/s13024-022-00538-8.
The dietary consumption of cuprizone - a copper chelator - has long been known to induce demyelination of specific brain structures and is widely used as model of multiple sclerosis. Despite the extensive use of cuprizone, the mechanism by which it induces demyelination are still unknown. With this review we provide an updated understanding of this model, by showcasing two distinct yet overlapping modes of action for cuprizone-induced demyelination; 1) damage originating from within the oligodendrocyte, caused by mitochondrial dysfunction or reduced myelin protein synthesis. We term this mode of action 'intrinsic cell damage'. And 2) damage to the oligodendrocyte exerted by inflammatory molecules, brain resident cells, such as oligodendrocytes, astrocytes, and microglia or peripheral immune cells - neutrophils or T-cells. We term this mode of action 'extrinsic cellular damage'. Lastly, we summarize recent developments in research on different forms of cell death induced by cuprizone, which could add valuable insights into the mechanisms of cuprizone toxicity. With this review we hope to provide a modern understanding of cuprizone-induced demyelination to understand the causes behind the demyelination in MS.
长期以来,饮食中摄入铜螯合剂——铜离子载体(cuprizone)——已被证实可导致特定脑区脱髓鞘,因此被广泛用作多发性硬化症(MS)的模型。尽管 cuprizone 被广泛应用,但导致脱髓鞘的确切机制仍不清楚。在本篇综述中,我们通过展示 cuprizone 诱导脱髓鞘的两种截然不同但又相互重叠的作用模式,为该模型提供了最新的认识:1)源自少突胶质细胞内部的损伤,由线粒体功能障碍或髓鞘蛋白合成减少引起。我们将这种作用模式称为“内在细胞损伤”。2)由炎症分子、脑固有细胞(如少突胶质细胞、星形胶质细胞和小胶质细胞)或外周免疫细胞(中性粒细胞或 T 细胞)对少突胶质细胞造成的损伤。我们将这种作用模式称为“外在细胞损伤”。最后,我们总结了 cuprizone 诱导的不同形式细胞死亡的最新研究进展,这可能为 cuprizone 毒性的机制提供有价值的见解。希望通过本篇综述,为理解 MS 中脱髓鞘的原因提供 cuprizone 诱导脱髓鞘的现代认识。