Demyelination Causes Synaptic Alterations in Hippocampi from Multiple Sclerosis Patients

被引:270
作者
Dutta, Ranjan [1 ]
Chang, Ansi [1 ]
Doud, Mary K. [1 ]
Kidd, Grahame J. [1 ]
Ribaudo, Michael V. [1 ]
Young, Elizabeth A. [1 ]
Fox, Robert J. [2 ]
Staugaitis, Susan M. [1 ,3 ]
Trapp, Bruce D. [1 ]
机构
[1] Cleveland Clin, Lerner Res Inst, Dept Neurosci, Cleveland, OH 44195 USA
[2] Cleveland Clin, Mellen Ctr Multiple Sclerosis Treatment & Res, Cleveland, OH 44195 USA
[3] Cleveland Clin, Dept Anat Pathol, Pathol & Lab Med Inst, Cleveland, OH 44195 USA
关键词
DEFICIENT MICE; PLASTICITY; MEMORY; MECHANISMS; NEURONS; NEUROGENESIS; LESIONS; DYSFUNCTION; ACTIVATION; TRANSPORT;
D O I
10.1002/ana.22337
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Objective: Multiple Sclerosis (MS) is an inflammatory demyelinating disease of the human central nervous system. Although the clinical impact of gray matter pathology in MS brains is unknown, 30 to 40% of MS patients demonstrate memory impairment. The molecular basis of this memory dysfunction has not yet been investigated in MS patients. Methods: To investigate possible mechanisms of memory impairment in MS patients, we compared morphological and molecular changes in myelinated and demyelinated hippocampi from postmortem MS brains. Results: Demyelinated hippocampi had minimal neuronal loss but significant decreases in synaptic density. Neuronal proteins essential for axonal transport, synaptic plasticity, glutamate neurotransmission, glutamate homeostasis, and memory/learning were significantly decreased in demyelinated hippocampi, but not in demyelinated motor cortices from MS brains. Interpretation: Collectively, these data support hippocampal demyelination as a cause of synaptic alterations in MS patients and establish that the neuronal genes regulated by myelination reflect specific functions of neuronal subpopulations. ANN NEUROL 2011;69:445-454
引用
收藏
页码:445 / 454
页数:10
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