多发性硬化症白质病变进展的空间分辨基因特征

IF 21.2 1区 医学 Q1 NEUROSCIENCES
Astrid M. Alsema, Marion H. C. Wijering, Anneke Miedema, Janssen M. Kotah, Mirjam Koster, Merel Rijnsburger, Hilmar R. J. van Weering, Helga E. de Vries, Wia Baron, Susanne M. Kooistra, Bart J. L. Eggen
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引用次数: 0

摘要

多发性硬化症(MS)是一种以髓鞘脱失和进行性神经变性为特征的中枢神经系统炎症性疾病。为了了解多发性硬化症病变的起始和进展,我们生成了多发性硬化症白质(WM)和灰质(GM)病变的空间基因表达图谱。在不同的多发性硬化症病变类型中,我们发现了具有不同基因特征的区域,包括活跃的 WM 病变周围可识别的边缘。星形胶质细胞特异性、少突胶质细胞特异性和小胶质细胞特异性基因组的表达变化是活动性病变边缘的特征。此外,我们还确定了三种 WM 病变进展轨迹,预测了外观正常的 WM 如何发展成 WM 活动性病变或活动-活动混合性病变。我们的数据揭示了多发性硬化病变的动态发展过程。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Spatially resolved gene signatures of white matter lesion progression in multiple sclerosis

Spatially resolved gene signatures of white matter lesion progression in multiple sclerosis

Multiple sclerosis (MS) is an inflammatory disease of the central nervous system characterized by myelin loss and progressive neurodegeneration. To understand MS lesion initiation and progression, we generate spatial gene expression maps of white matter (WM) and grey matter (GM) MS lesions. In different MS lesion types, we detect domains characterized by a distinct gene signature, including an identifiable rim around active WM lesions. Expression changes in astrocyte-specific, oligodendrocyte-specific and microglia-specific gene sets characterize the active lesion rims. Furthermore, we identify three WM lesion progression trajectories, predicting how normal-appearing WM can develop into WM active or mixed active–inactive lesions. Our data shed light on the dynamic progression of MS lesions.

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来源期刊
Nature neuroscience
Nature neuroscience 医学-神经科学
CiteScore
38.60
自引率
1.20%
发文量
212
审稿时长
1 months
期刊介绍: Nature Neuroscience, a multidisciplinary journal, publishes papers of the utmost quality and significance across all realms of neuroscience. The editors welcome contributions spanning molecular, cellular, systems, and cognitive neuroscience, along with psychophysics, computational modeling, and nervous system disorders. While no area is off-limits, studies offering fundamental insights into nervous system function receive priority. The journal offers high visibility to both readers and authors, fostering interdisciplinary communication and accessibility to a broad audience. It maintains high standards of copy editing and production, rigorous peer review, rapid publication, and operates independently from academic societies and other vested interests. In addition to primary research, Nature Neuroscience features news and views, reviews, editorials, commentaries, perspectives, book reviews, and correspondence, aiming to serve as the voice of the global neuroscience community.
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