多发性硬化症白质病变星形胶质细胞中脑脊液疾病标志物嗜铬粒蛋白A和聚簇蛋白的表达升高

Marvin M. van Luijn, M. van Meurs, M. Stoop, E. Verbraak, A. Wierenga-wolf, M. Melief, K. Kreft, R. Verdijk, B. '. ’t Hart, T. Luider, J. Laman, R. Hintzen
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引用次数: 19

摘要

利用蛋白质组学,我们先前在多发性硬化症(MS)患者的脑脊液(CSF)中发现了嗜铬粒蛋白A (CgA)和聚簇蛋白(CLU)作为疾病相关蛋白。CgA和CLU参与细胞存活,与神经退行性疾病有关,也可能在MS病理生理中起作用。我们研究了CgA和CLU在MS患者和对照组死后大脑病变和非病变区域以及实验性自身免疫性脑脊髓炎狨猴大脑中的表达。通过定量PCR, MS患者白质中CgA和CLU mRNA水平升高,而灰质中无升高。原位分析显示,在MS患者和狨猴的白质病变中,CgA和CLU的表达高于正常区域,主要是在血管周围间隙和炎症浸润内或附近。这两种蛋白均由胶质原纤维酸性蛋白阳性星形胶质细胞表达。CgA多局限于血管周围的星形细胞突起和终足,并大量存在于浅表胶质细胞边界和室管膜,2 csf -脑边界。在MS白质病变的反应性星形胶质细胞中,CgA和CLU的表达增加,支持了这些分子作为神经炎症介质的作用,以及它们作为MS患者活跃病理过程的CSF标志物的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Elevated Expression of the Cerebrospinal Fluid Disease Markers Chromogranin A and Clusterin in Astrocytes of Multiple Sclerosis White Matter Lesions
Using proteomics, we previously identified chromogranin A (CgA) and clusterin (CLU) as disease-related proteins in the cerebrospinal fluid (CSF) of patients with multiple sclerosis (MS). CgA and CLU are involved in cell survival and are implicated in neurodegenerative disorders and may also have roles in MS pathophysiology. We investigated CgA and CLU expression in lesions and nonlesional regions in postmortem brains of MS patients and controls and in the brains of marmosets with experimental autoimmune encephalomyelitis. By quantitative PCR, mRNA levels of CgA and CLU were elevated in white matter but not in grey matter of MS patients. In situ analyses showed greater expression of CgA and CLU in white matter lesions than in normal-appearing regions in MS patients and in the marmosets, primarily in or adjacent to perivascular spaces and inflammatory infiltrates. Both proteins were expressed by glial fibrillary acidic protein-positive astrocytes. CgA was more localized in astrocytic processes and endfeet surrounding blood vessels and was abundant in the superficial glia limitans and ependyma, 2 CSF-brain borders. Increased expression of CgA and CLU in reactive astrocytes in MS white matter lesions supports a role for these molecules as neuro-inflammatory mediators and their potential as CSF markers of active pathological processes in MS patients.
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