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早期多发性硬化症中与活动性脱髓鞘病变相邻的白质分子变化

Molecular changes in white matter adjacent to an active demyelinating lesion in early multiple sclerosis.

作者信息

Zeis Thomas, Probst Alfonse, Steck Andreas Johann, Stadelmann Christine, Brück Wolfgang, Schaeren-Wiemers Nicole

机构信息

Neurobiology, Department of Biomedicine and Neurology, University Hospital Basel, Pharmacenter, Basel, Switzerland.

出版信息

Brain Pathol. 2009 Jul;19(3):459-66. doi: 10.1111/j.1750-3639.2008.00231.x. Epub 2008 Oct 31.

Abstract

A stereotactic biopsy of a 17-year-old woman revealed an active inflammatory demyelinating lesion compatible with pattern III multiple sclerosis (MS) according to Lucchinetti et al. The biopsy included a white matter region distant from the active inflammatory demyelinating lesion with abnormal MRI signal, lacking histopathological signs of demyelination and/or oligodendrocyte apoptosis. Expression analysis of this area revealed a strong up-regulation of neuronal nitric oxide synthase (nNOS). Furthermore, detection of nitrotyrosine provided evidence for reactive nitrogen species (RNS)-mediated damage to oligodendrocytes. Concomitantly, genes involved in neuroprotection against oxidative stress such as heme oxygenase 1 were up-regulated. Even though a single case report, this study shows earliest molecular changes in white matter surrounding an actively demyelinating lesion during the first manifestation of MS, pointing toward a more widespread pathological process. Therapeutic targeting of the identified mechanisms of tissue injury might be crucial to prevent further lesion formation or secondary tissue damage.

摘要

对一名17岁女性进行的立体定向活检显示,根据卢基尼蒂等人的标准,存在一个与III型多发性硬化症(MS)相符的活动性炎性脱髓鞘病变。活检包括一个远离活动性炎性脱髓鞘病变且MRI信号异常的白质区域,该区域缺乏脱髓鞘和/或少突胶质细胞凋亡的组织病理学迹象。对该区域的表达分析显示神经元型一氧化氮合酶(nNOS)强烈上调。此外,硝基酪氨酸的检测为活性氮物质(RNS)介导的少突胶质细胞损伤提供了证据。同时,参与对抗氧化应激的神经保护相关基因,如血红素加氧酶1也上调。尽管这是一项单病例报告,但该研究显示了MS首次发作时活动性脱髓鞘病变周围白质最早的分子变化,表明存在更广泛的病理过程。针对已确定的组织损伤机制进行治疗靶向可能对预防进一步的病变形成或继发性组织损伤至关重要。

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本文引用的文献

1
Lame ducks or fierce creatures? The role of oligodendrocytes in multiple sclerosis.
J Mol Neurosci. 2008 May;35(1):91-100. doi: 10.1007/s12031-008-9042-1. Epub 2008 Feb 16.
2
Normal-appearing white matter in multiple sclerosis is in a subtle balance between inflammation and neuroprotection.
Brain. 2008 Jan;131(Pt 1):288-303. doi: 10.1093/brain/awm291. Epub 2007 Dec 4.
5
Imaging correlates of axonal swelling in chronic multiple sclerosis brains.
Ann Neurol. 2007 Sep;62(3):219-28. doi: 10.1002/ana.21113.
6
Heme oxygenase-1 and carbon monoxide suppress autoimmune neuroinflammation.
J Clin Invest. 2007 Feb;117(2):438-47. doi: 10.1172/JCI28844. Epub 2007 Jan 25.
7
Neuronal nitric oxide synthase plays a key role in CNS demyelination.
J Neurosci. 2006 Dec 6;26(49):12672-81. doi: 10.1523/JNEUROSCI.0294-06.2006.
8
Revisions to the 2001 McDonald diagnostic criteria.
Ann Neurol. 2006 Apr;59(4):727-8. doi: 10.1002/ana.20826.
9
STAT4- and STAT6-signaling molecules in a murine model of multiple sclerosis.
FASEB J. 2006 Feb;20(2):343-5. doi: 10.1096/fj.05-4650fje. Epub 2005 Dec 13.
10
Carbon monoxide mediates protection against nitric oxide toxicity in HeLa cells.
Free Radic Biol Med. 2005 Oct 15;39(8):1075-88. doi: 10.1016/j.freeradbiomed.2005.05.023.

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