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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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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E. ; Amor, S. ; Bø, L. ; Dijkstra, C. D. ; Van Der Valk, P. ; Geurts, J. J. G.</creator><creatorcontrib>Kooi, E.-J. ; Van Horssen, J. ; Witte, M. E. ; Amor, S. ; Bø, L. ; Dijkstra, C. D. ; Van Der Valk, P. ; Geurts, J. J. G.</creatorcontrib><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.</description><identifier>ISSN: 0305-1846</identifier><identifier>EISSN: 1365-2990</identifier><identifier>DOI: 10.1111/j.1365-2990.2008.00986.x</identifier><identifier>PMID: 19473295</identifier><identifier>CODEN: NANEDL</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>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</subject><ispartof>Neuropathology and applied neurobiology, 2009-06, Vol.35 (3), p.283-295</ispartof><rights>2009 Blackwell Publishing Ltd</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5156-e28bfc4762dfb3ce86a6057280151551ae78fee93565b6866c44d3fce6dfe2163</citedby><cites>FETCH-LOGICAL-c5156-e28bfc4762dfb3ce86a6057280151551ae78fee93565b6866c44d3fce6dfe2163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2990.2008.00986.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2990.2008.00986.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,777,781,1412,27905,27906,45555,45556</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21376086$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19473295$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kooi, E.-J.</creatorcontrib><creatorcontrib>Van Horssen, J.</creatorcontrib><creatorcontrib>Witte, M. 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. This may be relevant for understanding sustained immunogenicity or, alternatively, tolerogenicity in MS.</description><subject>Adolescent</subject><subject>Adrenoleukodystrophy - metabolism</subject><subject>Adrenoleukodystrophy - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Alzheimer Disease - metabolism</subject><subject>Alzheimer Disease - pathology</subject><subject>Biological and medical sciences</subject><subject>Brain - blood supply</subject><subject>Brain - metabolism</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Dendritic Cells - metabolism</subject><subject>extracellular</subject><subject>Extracellular Space - chemistry</subject><subject>Female</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Macrophages - metabolism</subject><subject>Male</subject><subject>Medical sciences</subject><subject>meninges</subject><subject>Meninges - chemistry</subject><subject>Meninges - pathology</subject><subject>Meningitis - metabolism</subject><subject>Meningitis - pathology</subject><subject>Middle Aged</subject><subject>multiple sclerosis</subject><subject>Multiple Sclerosis - metabolism</subject><subject>Multiple Sclerosis - pathology</subject><subject>myelin</subject><subject>Myelin Proteins - analysis</subject><subject>Myelin Sheath - chemistry</subject><subject>Myelin Sheath - pathology</subject><subject>Neurology</subject><subject>Stroke - metabolism</subject><subject>Stroke - pathology</subject><subject>Viral diseases</subject><subject>Viral diseases of the nervous system</subject><issn>0305-1846</issn><issn>1365-2990</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkE2P0zAQhi0EYsvCX0C-wC3BH7FjS1zKChbQbtFKRRwtx5mwLk5aYkfb_nucbVWOYFnyYZ7XM_MghCkpaT7vNiXlUhRMa1IyQlRJiFay3D9Bi3PhKVoQTkRBVSUv0IsYN4QQUUv9HF1QXdWcabFAd8tmGlo7JAz7NFoHIUzBjrg_QPADzjfdA-5h8MNPiHjb4Z1NHoYU8YNP97ifQvK7ADi6AOM2-vgSPetsiPDq9F6i758-rq8-Fzffrr9cLW8KJ6iQBTDVdK6qJWu7hjtQ0so8HlOE5rqgFmrVAWgupGikktJVVcs7B7LtgFHJL9Hb47-7cft7gphM7-M8vx1gO0Uj81-UVtU_QUZElZvqDKoj6PIicYTO7Ebf2_FgKDGzd7Mxs14z6zWzd_Po3exz9PWpx9T00P4NnkRn4M0JsNHZ0I12cD6eOUZ5LYmat3p_5B58gMN_D2BWy5V-jBfHuI8J9ue4HX9lH7wW5sfq2tzerT_cCvnVrPkfK7itqA</recordid><startdate>200906</startdate><enddate>200906</enddate><creator>Kooi, E.-J.</creator><creator>Van Horssen, J.</creator><creator>Witte, M. E.</creator><creator>Amor, S.</creator><creator>Bø, L.</creator><creator>Dijkstra, C. D.</creator><creator>Van Der Valk, P.</creator><creator>Geurts, J. J. G.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope></search><sort><creationdate>200906</creationdate><title>Abundant extracellular myelin in the meninges of patients with multiple sclerosis</title><author>Kooi, E.-J. ; Van Horssen, J. ; Witte, M. E. ; Amor, S. ; Bø, L. ; Dijkstra, C. D. ; Van Der Valk, P. ; Geurts, J. J. G.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5156-e28bfc4762dfb3ce86a6057280151551ae78fee93565b6866c44d3fce6dfe2163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adolescent</topic><topic>Adrenoleukodystrophy - metabolism</topic><topic>Adrenoleukodystrophy - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Alzheimer Disease - metabolism</topic><topic>Alzheimer Disease - pathology</topic><topic>Biological and medical sciences</topic><topic>Brain - blood supply</topic><topic>Brain - metabolism</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Dendritic Cells - metabolism</topic><topic>extracellular</topic><topic>Extracellular Space - chemistry</topic><topic>Female</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Macrophages - metabolism</topic><topic>Male</topic><topic>Medical sciences</topic><topic>meninges</topic><topic>Meninges - chemistry</topic><topic>Meninges - pathology</topic><topic>Meningitis - metabolism</topic><topic>Meningitis - pathology</topic><topic>Middle Aged</topic><topic>multiple sclerosis</topic><topic>Multiple Sclerosis - metabolism</topic><topic>Multiple Sclerosis - pathology</topic><topic>myelin</topic><topic>Myelin Proteins - analysis</topic><topic>Myelin Sheath - chemistry</topic><topic>Myelin Sheath - pathology</topic><topic>Neurology</topic><topic>Stroke - metabolism</topic><topic>Stroke - pathology</topic><topic>Viral diseases</topic><topic>Viral diseases of the nervous system</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kooi, E.-J.</creatorcontrib><creatorcontrib>Van Horssen, J.</creatorcontrib><creatorcontrib>Witte, M. 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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