Molecular Changes in White Matter Adjacent to an Active Demyelinating Lesion in Early Multiple Sclerosis

被引:56
|
作者
Zeis, Thomas [1 ]
Probst, Alfonse [2 ]
Steck, Andreas Johann [1 ]
Stadelmann, Christine [3 ]
Brueck, Wolfgang [3 ]
Schaeren-Wiemers, Nicole [1 ]
机构
[1] Univ Basel Hosp, Dept Biomed & Neurol, Pharmactr, CH-4056 Basel, Switzerland
[2] Univ Basel Hosp, Inst Neuropathol, CH-4056 Basel, Switzerland
[3] Univ Gottingen, Inst Neuropathol, Gottingen, Germany
关键词
multiple sclerosis; oligodendrocyte pathology; oxidative stress; white matter injury; HYPOXIA-INDUCIBLE FACTOR-1; NITRIC-OXIDE; OLIGODENDROCYTE INJURY; OXIDATIVE STRESS; HEME OXYGENASE-1; CELLS; ASTROCYTES; EXPRESSION; DISEASE;
D O I
10.1111/j.1750-3639.2008.00231.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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.
引用
收藏
页码:459 / 466
页数:8
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