Abundant extracellular myelin in the meninges of patients with multiple sclerosis

被引:36
作者
Kooi, E-J. [1 ]
van Horssen, J. [1 ,2 ]
Witte, M. E. [1 ]
Amor, S. [1 ,4 ]
Bo, L. [5 ]
Dijkstra, C. D. [2 ]
van der Valk, P. [1 ]
Geurts, J. J. G. [1 ,3 ]
机构
[1] Vrije Univ Amsterdam Med Ctr, Dept Pathol Neuropathol, NL-1081 HV Amsterdam, Netherlands
[2] Vrije Univ Amsterdam Med Ctr, Dept Mol Cell Biol & Immunol, NL-1081 HV Amsterdam, Netherlands
[3] Vrije Univ Amsterdam Med Ctr, Dept Radiol, NL-1081 HV Amsterdam, Netherlands
[4] Queen Mary Univ London, Neuroimmunol Unit, Ctr Neurosci, Inst Cell & Mol Sci, London, England
[5] Univ Bergen, Dept Neurol, Haukeland Univ Hosp, N-5014 Bergen, Norway
关键词
extracellular; meninges; multiple sclerosis; myelin; CENTRAL-NERVOUS-SYSTEM; CERVICAL LYMPH-NODES; B-CELL FOLLICLES; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; EXPERIMENTAL ALLERGIC ENCEPHALOMYELITIS; CEREBROSPINAL-FLUID SEDIMENT; CEREBRAL AMYLOID ANGIOPATHY; INTERSTITIAL FLUID; DENDRITIC CELLS; BASIC-PROTEIN;
D O I
10.1111/j.1365-2990.2008.00986.x
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: In multiple sclerosis (MS) myelin debris has been observed within MS lesions, in cerebrospinal fluid and cervical lymph nodes, but the route of myelin transport out of the brain is unknown. Drainage of interstitial fluid from the brain parenchyma involves the perivascular spaces and leptomeninges, but the presence of myelin debris in these compartments has not been described. Aims: To determine whether myelin products are present in the meninges and perivascular spaces of MS patients. Methods: Formalin-fixed brain tissue containing meninges from 29 MS patients, 9 non-neurological controls, 6 Alzheimer's disease, 5 stroke, 5 meningitis and 7 leucodystrophy patients was investigated, and immunohistochemically stained for several myelin proteins [proteolipid protein (PLP), myelin basic protein (MBP), myelin oligodendrocyte glycoprotein (MOG) and 2',3'-cyclic nucleotide 3'-phosphodiesterase (CNPase)]. On brain material from MS patients and (non)neurological controls, PLP immunostaining was used to systematically investigate the presence of myelin debris in the meninges, using a semiquantitative scale. Results: Extensive extracellular presence of myelin particles, positive for PLP, MBP, MOG and CNPase in the leptomeninges of MS patients, was observed. Myelin particles were also observed in perivascular spaces of MS patients. Immunohistochemical double-labelling for macrophage and dendritic cell markers and PLP confirmed that the vast majority of myelin particles were located extracellularly. Extracellular myelin particles were virtually absent in meningeal tissue of non-neurological controls, Alzheimer's disease, stroke, meningitis and leucodystrophy cases. Conclusions: In MS leptomeninges and perivascular spaces, abundant extracellular myelin can be found, whereas this is not the case for controls and other neurological disease. This may be relevant for understanding sustained immunogenicity or, alternatively, tolerogenicity in MS.
引用
收藏
页码:283 / 295
页数:13
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