血管周围胶质反应性是慢性外伤性脑病中磷酸化tau病变的一个特征

IF 9.3 1区 医学 Q1 CLINICAL NEUROLOGY
Chelsie Osterman, Danica Hamlin, Catherine M. Suter, Andrew J. Affleck, Brian S. Gloss, Clinton P. Turner, Richard L. M. Faull, Thor D. Stein, Ann McKee, Michael E. Buckland, Maurice A. Curtis, Helen C. Murray
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引用次数: 0

摘要

慢性创伤性脑病(CTE)是一种与重复性头部损伤相关的神经退行性疾病,其特征是皮层脑沟深处血管周围过度磷酸化的tau蛋白(p-tau)积累。尽管大多数CTE文献关注的是p-tau病理,但其他病理特征,如神经胶质反应性、血管损伤和轴突损伤等相对未被探索。在这项研究中,我们旨在表征这些其他病理特征,特别是在CTE p-tau病变区域,以更好地了解病变周围的微环境。我们利用多重免疫组织化学研究了与创伤性脑损伤和神经变性相关的32种不同的细胞结构和病理标志物的分布。我们定性地评估了多重图像,并测量了CTE病例病变和非病变区域中每个标记物的标记面积百分比。我们发现血管周围胶质反应性是CTE p-tau病变的一个突出特征,主要是由于星形胶质细胞反应性比非病变区域增加。此外,我们还发现了标记有NAD(P)H醌脱氢酶1 (NQO1)和l -铁蛋白的星形胶质细胞,这表明病变相关的胶质反应性可能是对铁诱导的氧化应激的代偿反应。我们的研究结果表明,血管周围炎症是CTE病理病变的一致特征,可能有助于脑损伤相关神经变性的发病机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Perivascular glial reactivity is a feature of phosphorylated tau lesions in chronic traumatic encephalopathy

Chronic traumatic encephalopathy (CTE), a neurodegenerative disease associated with repetitive head injuries, is characterised by perivascular hyperphosphorylated tau (p-tau) accumulations within the depths of cortical sulci. Although the majority of CTE literature focuses on p-tau pathology, other pathological features such as glial reactivity, vascular damage, and axonal damage are relatively unexplored. In this study, we aimed to characterise these other pathological features, specifically in CTE p-tau lesion areas, to better understand the microenvironment surrounding the lesion. We utilised multiplex immunohistochemistry to investigate the distribution of 32 different markers of cytoarchitecture and pathology that are relevant to both traumatic brain injury and neurodegeneration. We qualitatively assessed the multiplex images and measured the percentage area of labelling for each marker in the lesion and non-lesion areas of CTE cases. We identified perivascular glial reactivity as a prominent feature of CTE p-tau lesions, largely driven by increases in astrocyte reactivity compared to non-lesion areas. Furthermore, we identified astrocytes labelled for both NAD(P)H quinone dehydrogenase 1 (NQO1) and L-ferritin, indicating that lesion-associated glial reactivity may be a compensatory response to iron-induced oxidative stress. Our findings demonstrate that perivascular inflammation is a consistent feature of the CTE pathognomonic lesion and may contribute to the pathogenesis of brain injury-related neurodegeneration.

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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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