Abundant extracellular myelin in the meninges of patients with multiple sclerosis

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 lept...

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Veröffentlicht in:Neuropathology and applied neurobiology 2009-06, Vol.35 (3), p.283-295
Hauptverfasser: Kooi, E.-J., Van Horssen, J., Witte, M. E., Amor, S., Bø, L., Dijkstra, C. D., Van Der Valk, P., Geurts, J. J. G.
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container_end_page 295
container_issue 3
container_start_page 283
container_title Neuropathology and applied neurobiology
container_volume 35
creator Kooi, E.-J.
Van Horssen, J.
Witte, M. E.
Amor, S.
Bø, L.
Dijkstra, C. D.
Van Der Valk, P.
Geurts, J. J. G.
description 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.
doi_str_mv 10.1111/j.1365-2990.2008.00986.x
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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. 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E.</creatorcontrib><creatorcontrib>Amor, S.</creatorcontrib><creatorcontrib>Bø, L.</creatorcontrib><creatorcontrib>Dijkstra, C. D.</creatorcontrib><creatorcontrib>Van Der Valk, P.</creatorcontrib><creatorcontrib>Geurts, J. J. G.</creatorcontrib><title>Abundant extracellular myelin in the meninges of patients with multiple sclerosis</title><title>Neuropathology and applied neurobiology</title><addtitle>Neuropathol Appl Neurobiol</addtitle><description>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. 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E.</creatorcontrib><creatorcontrib>Amor, S.</creatorcontrib><creatorcontrib>Bø, L.</creatorcontrib><creatorcontrib>Dijkstra, C. D.</creatorcontrib><creatorcontrib>Van Der Valk, P.</creatorcontrib><creatorcontrib>Geurts, J. J. G.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Neuropathology and applied neurobiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kooi, E.-J.</au><au>Van Horssen, J.</au><au>Witte, M. E.</au><au>Amor, S.</au><au>Bø, L.</au><au>Dijkstra, C. D.</au><au>Van Der Valk, P.</au><au>Geurts, J. J. G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abundant extracellular myelin in the meninges of patients with multiple sclerosis</atitle><jtitle>Neuropathology and applied neurobiology</jtitle><addtitle>Neuropathol Appl Neurobiol</addtitle><date>2009-06</date><risdate>2009</risdate><volume>35</volume><issue>3</issue><spage>283</spage><epage>295</epage><pages>283-295</pages><issn>0305-1846</issn><eissn>1365-2990</eissn><coden>NANEDL</coden><abstract>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.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>19473295</pmid><doi>10.1111/j.1365-2990.2008.00986.x</doi><tpages>13</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adrenoleukodystrophy - metabolism
Adrenoleukodystrophy - pathology
Adult
Aged
Aged, 80 and over
Alzheimer Disease - metabolism
Alzheimer Disease - pathology
Biological and medical sciences
Brain - blood supply
Brain - metabolism
Child
Child, Preschool
Dendritic Cells - metabolism
extracellular
Extracellular Space - chemistry
Female
Human viral diseases
Humans
Infectious diseases
Macrophages - metabolism
Male
Medical sciences
meninges
Meninges - chemistry
Meninges - pathology
Meningitis - metabolism
Meningitis - pathology
Middle Aged
multiple sclerosis
Multiple Sclerosis - metabolism
Multiple Sclerosis - pathology
myelin
Myelin Proteins - analysis
Myelin Sheath - chemistry
Myelin Sheath - pathology
Neurology
Stroke - metabolism
Stroke - pathology
Viral diseases
Viral diseases of the nervous system
title Abundant extracellular myelin in the meninges of patients with multiple sclerosis
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