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利用人脑组织微阵列阐明亨廷顿舞蹈病中的皮质神经血管受累情况。

Elucidating cortical neurovascular involvement in Huntington's disease using human brain tissue microarrays.

作者信息

Tan Adelie Y S, Martinez Lance C M G, Murray Helen C, Mehrabi Nasim F, Tippett Lynette J, Turner Clinton P, Curtis Maurice A, Faull Richard L M, Dragunow Mike, Singh-Bains Malvindar K

机构信息

Centre for Brain Research, University of Auckland, Auckland 1023, New Zealand; Department of Anatomy and Medical Imaging, University of Auckland, Auckland 1023, New Zealand.

Centre for Brain Research, University of Auckland, Auckland 1023, New Zealand; Department of Pharmacology and Clinical Pharmacology, University of Auckland, Auckland 1023, New Zealand.

出版信息

Neurobiol Dis. 2025 Mar;206:106829. doi: 10.1016/j.nbd.2025.106829. Epub 2025 Feb 3.

Abstract

Although the genetic basis of Huntington's disease (HD) has been determined, the underlying pathophysiological mechanisms contributing to neurodegeneration remain largely unknown. In recent years, increasing evidence has posited vascular dysfunction as a significant early event in disease pathogenesis; however, these processes remain to be fully elucidated. High-content immunohistochemical screening studies were conducted on HD middle temporal gyrus (MTG) human brain tissue microarrays (TMAs) to investigate various components of the vascular system, including endothelial cells (UEA-1), pericytes (PDGFRβ), vascular smooth muscle cells (αSMA), extracellular matrix components (ECM; collagen IV and fibronectin), and leakage markers (haemoglobin and fibrinogen). Analyses of vascular markers revealed an increase in the number of vessels in the HD TMA cohort which was associated with advancing striatal pathology and earlier symptom onset. Furthermore, our findings highlight the preservation of pericytes, vascular smooth muscle cells, ECM components, and blood-brain barrier integrity in the HD MTG. Collectively, the TMA findings allude to mild vascular remodelling in the temporal cortex which is known to present with a lesser degree of neuronal degeneration in HD.

摘要

尽管亨廷顿舞蹈症(HD)的遗传基础已被确定,但导致神经退行性变的潜在病理生理机制在很大程度上仍不清楚。近年来,越来越多的证据表明血管功能障碍是疾病发病机制中的一个重要早期事件;然而,这些过程仍有待充分阐明。我们对HD中颞叶回(MTG)人脑组织微阵列(TMA)进行了高内涵免疫组化筛选研究,以调查血管系统的各种成分,包括内皮细胞(UEA-1)、周细胞(PDGFRβ)、血管平滑肌细胞(αSMA)、细胞外基质成分(ECM;IV型胶原和纤连蛋白)以及渗漏标志物(血红蛋白和纤维蛋白原)。对血管标志物的分析显示,HD TMA队列中的血管数量增加,这与纹状体病理进展和症状提前出现有关。此外,我们的研究结果突出了HD MTG中周细胞、血管平滑肌细胞、ECM成分以及血脑屏障完整性的保留。总体而言,TMA研究结果表明颞叶皮质存在轻度血管重塑,而HD中该区域的神经元变性程度较轻。

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