坏死细胞死亡途径驱动阿尔茨海默病的神经变性。

IF 9.3 1区 医学 Q1 CLINICAL NEUROLOGY
Sriram Balusu, Bart De Strooper
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引用次数: 0

摘要

虽然凋亡、热凋亡和铁凋亡都与 AD 有关,但它们都不能完全解释在 AD 大脑中观察到的大量神经元丢失。最近的证据表明,坏死在AD中大量存在,坏死与Tau病理学的出现密切相关,而且坏死标记物在颗粒细胞神经变性囊泡中积聚。我们在此回顾了粒细胞介导的神经元-坏死通路的神经元特异性激活、该通路上游的潜在AD相关诱因、坏死体与内溶酶体通路的相互作用,这些可能与Tau病理学有关。此外,我们还强调了抑制坏死蛋白沉积对神经退行性疾病(如阿氏痴呆症)的治疗潜力,因为这为针对神经元缺失以保护认知能力的药物开发提供了一条新途径。当这种方法与降低淀粉样蛋白的药物相结合时,似乎尤为重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The necroptosis cell death pathway drives neurodegeneration in Alzheimer's disease.

The necroptosis cell death pathway drives neurodegeneration in Alzheimer's disease.

Although apoptosis, pyroptosis, and ferroptosis have been implicated in AD, none fully explains the extensive neuronal loss observed in AD brains. Recent evidence shows that necroptosis is abundant in AD, that necroptosis is closely linked to the appearance of Tau pathology, and that necroptosis markers accumulate in granulovacuolar neurodegeneration vesicles (GVD). We review here the neuron-specific activation of the granulovacuolar mediated neuronal-necroptosis pathway, the potential AD-relevant triggers upstream of this pathway, and the interaction of the necrosome with the endo-lysosomal pathway, possibly providing links to Tau pathology. In addition, we underscore the therapeutic potential of inhibiting necroptosis in neurodegenerative diseases such as AD, as this presents a novel avenue for drug development targeting neuronal loss to preserve cognitive abilities. Such an approach seems particularly relevant when combined with amyloid-lowering drugs.

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来源期刊
Acta Neuropathologica
Acta Neuropathologica 医学-病理学
CiteScore
23.70
自引率
3.90%
发文量
118
审稿时长
4-8 weeks
期刊介绍: Acta Neuropathologica publishes top-quality papers on the pathology of neurological diseases and experimental studies on molecular and cellular mechanisms using in vitro and in vivo models, ideally validated by analysis of human tissues. The journal accepts Original Papers, Review Articles, Case Reports, and Scientific Correspondence (Letters). Manuscripts must adhere to ethical standards, including review by appropriate ethics committees for human studies and compliance with principles of laboratory animal care for animal experiments. Failure to comply may result in rejection of the manuscript, and authors are responsible for ensuring accuracy and adherence to these requirements.
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