Distinct gene expression in demyelinated white and grey matter areas of patients with multiple sclerosis

Abstract Demyelination of the central nervous system is a prominent pathological hallmark of multiple sclerosis and affects both white and grey matter. However, demyelinated white and grey matter exhibit clear pathological differences, most notably the presence or absence of inflammation and activat...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Brain communications 2022, Vol.4 (2), p.fcac005-fcac005
Hauptverfasser: van Wageningen, Thecla A., Gerrits, Emma, Brouwer, Nieske, Brevé, John J. P., Geurts, Jeroen J. G., Eggen, Bart J. L., Boddeke, H. W. G. M. (Erik), van Dam, Anne-Marie
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page fcac005
container_issue 2
container_start_page fcac005
container_title Brain communications
container_volume 4
creator van Wageningen, Thecla A.
Gerrits, Emma
Brouwer, Nieske
Brevé, John J. P.
Geurts, Jeroen J. G.
Eggen, Bart J. L.
Boddeke, H. W. G. M. (Erik)
van Dam, Anne-Marie
description Abstract Demyelination of the central nervous system is a prominent pathological hallmark of multiple sclerosis and affects both white and grey matter. However, demyelinated white and grey matter exhibit clear pathological differences, most notably the presence or absence of inflammation and activated glial cells in white and grey matter, respectively. In order to gain more insight into the differential pathology of demyelinated white and grey matter areas, we micro-dissected neighbouring white and grey matter demyelinated areas as well as normal-appearing matter from leucocortical lesions of human post-mortem material and used these samples for RNA sequencing. Our data show that even neighbouring demyelinated white and grey matter of the same leucocortical have a distinct gene expression profile and cellular composition. We propose that, based on their distinct expression profile, pathological processes in neighbouring white and grey matter are likely different which could have implications for the efficacy of treating grey matter lesions with current anti-inflammatory-based multiple sclerosis drugs. van Wageningen et al. present gene expression data of demyelinated and normal-appearing white and grey matter of multiple sclerosis leucocortical lesions. They find that grey matter lesions primarily feature gene expression indicative of a microglial response while white matter lesions feature astrocytic activation and dystrophic neurons. Graphical Abstract Graphical Abstract
doi_str_mv 10.1093/braincomms/fcac005
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8914505</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><oup_id>10.1093/braincomms/fcac005</oup_id><sourcerecordid>2638959815</sourcerecordid><originalsourceid>FETCH-LOGICAL-c440t-21c1b404f97439121dd99c640d8cfa4f5ff91473f3a54093aa21aab3d117eccc3</originalsourceid><addsrcrecordid>eNqNkctuFDEQRS1ERKIkP8ACecmmiZ8z7Q0SCk8pEptkbdW4yzNG3XZju0nm73E0Qwg7VlVS3Tr1uIS85uwdZ0ZebTKE6NI0lSvvwDGmX5AzsZKi48KsXz7LT8llKT8YY0IrLU3_ipxKLXrBV-KM7D6GUhuo0i1GpPgwZywlpEhDpANOexxDhIoDvd-FihTiQLcZ93SCWjFTyAiFJk9nqAFjLfQ-1B2dlrGGeURa3Ig5lVAuyImHseDlMZ6Tu8-fbq-_djffv3y7_nDTOaVY7QR3fKOY8matpOGCD4MxbqXY0DsPymvvDVdr6SVo1f4AIDjARg6cr9E5J8_J-wN3XjYTDq7tlGG0cw4T5L1NEOy_lRh2dpt-2b5xNdMN8PYIyOnngqXaKRSH4wgR01Js-2tvtOn5o1QcpK6dWDL6pzGc2UeX7F-X7NGl1vTm-YJPLX88aYLuIEjL_D_A398IpSE</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2638959815</pqid></control><display><type>article</type><title>Distinct gene expression in demyelinated white and grey matter areas of patients with multiple sclerosis</title><source>DOAJ Directory of Open Access Journals</source><source>Oxford Journals Open Access Collection</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><creator>van Wageningen, Thecla A. ; Gerrits, Emma ; Brouwer, Nieske ; Brevé, John J. P. ; Geurts, Jeroen J. G. ; Eggen, Bart J. L. ; Boddeke, H. W. G. M. (Erik) ; van Dam, Anne-Marie</creator><creatorcontrib>van Wageningen, Thecla A. ; Gerrits, Emma ; Brouwer, Nieske ; Brevé, John J. P. ; Geurts, Jeroen J. G. ; Eggen, Bart J. L. ; Boddeke, H. W. G. M. (Erik) ; van Dam, Anne-Marie</creatorcontrib><description>Abstract Demyelination of the central nervous system is a prominent pathological hallmark of multiple sclerosis and affects both white and grey matter. However, demyelinated white and grey matter exhibit clear pathological differences, most notably the presence or absence of inflammation and activated glial cells in white and grey matter, respectively. In order to gain more insight into the differential pathology of demyelinated white and grey matter areas, we micro-dissected neighbouring white and grey matter demyelinated areas as well as normal-appearing matter from leucocortical lesions of human post-mortem material and used these samples for RNA sequencing. Our data show that even neighbouring demyelinated white and grey matter of the same leucocortical have a distinct gene expression profile and cellular composition. We propose that, based on their distinct expression profile, pathological processes in neighbouring white and grey matter are likely different which could have implications for the efficacy of treating grey matter lesions with current anti-inflammatory-based multiple sclerosis drugs. van Wageningen et al. present gene expression data of demyelinated and normal-appearing white and grey matter of multiple sclerosis leucocortical lesions. They find that grey matter lesions primarily feature gene expression indicative of a microglial response while white matter lesions feature astrocytic activation and dystrophic neurons. Graphical Abstract Graphical Abstract</description><identifier>ISSN: 2632-1297</identifier><identifier>EISSN: 2632-1297</identifier><identifier>DOI: 10.1093/braincomms/fcac005</identifier><identifier>PMID: 35282162</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Original</subject><ispartof>Brain communications, 2022, Vol.4 (2), p.fcac005-fcac005</ispartof><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain. 2022</rights><rights>The Author(s) 2022. Published by Oxford University Press on behalf of the Guarantors of Brain.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-21c1b404f97439121dd99c640d8cfa4f5ff91473f3a54093aa21aab3d117eccc3</citedby><cites>FETCH-LOGICAL-c440t-21c1b404f97439121dd99c640d8cfa4f5ff91473f3a54093aa21aab3d117eccc3</cites><orcidid>0000-0001-7248-8779 ; 0000-0003-1896-3748 ; 0000-0002-5304-9487</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914505/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC8914505/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,864,885,1604,4023,27922,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35282162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>van Wageningen, Thecla A.</creatorcontrib><creatorcontrib>Gerrits, Emma</creatorcontrib><creatorcontrib>Brouwer, Nieske</creatorcontrib><creatorcontrib>Brevé, John J. P.</creatorcontrib><creatorcontrib>Geurts, Jeroen J. G.</creatorcontrib><creatorcontrib>Eggen, Bart J. L.</creatorcontrib><creatorcontrib>Boddeke, H. W. G. M. (Erik)</creatorcontrib><creatorcontrib>van Dam, Anne-Marie</creatorcontrib><title>Distinct gene expression in demyelinated white and grey matter areas of patients with multiple sclerosis</title><title>Brain communications</title><addtitle>Brain Commun</addtitle><description>Abstract Demyelination of the central nervous system is a prominent pathological hallmark of multiple sclerosis and affects both white and grey matter. However, demyelinated white and grey matter exhibit clear pathological differences, most notably the presence or absence of inflammation and activated glial cells in white and grey matter, respectively. In order to gain more insight into the differential pathology of demyelinated white and grey matter areas, we micro-dissected neighbouring white and grey matter demyelinated areas as well as normal-appearing matter from leucocortical lesions of human post-mortem material and used these samples for RNA sequencing. Our data show that even neighbouring demyelinated white and grey matter of the same leucocortical have a distinct gene expression profile and cellular composition. We propose that, based on their distinct expression profile, pathological processes in neighbouring white and grey matter are likely different which could have implications for the efficacy of treating grey matter lesions with current anti-inflammatory-based multiple sclerosis drugs. van Wageningen et al. present gene expression data of demyelinated and normal-appearing white and grey matter of multiple sclerosis leucocortical lesions. They find that grey matter lesions primarily feature gene expression indicative of a microglial response while white matter lesions feature astrocytic activation and dystrophic neurons. Graphical Abstract Graphical Abstract</description><subject>Original</subject><issn>2632-1297</issn><issn>2632-1297</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNqNkctuFDEQRS1ERKIkP8ACecmmiZ8z7Q0SCk8pEptkbdW4yzNG3XZju0nm73E0Qwg7VlVS3Tr1uIS85uwdZ0ZebTKE6NI0lSvvwDGmX5AzsZKi48KsXz7LT8llKT8YY0IrLU3_ipxKLXrBV-KM7D6GUhuo0i1GpPgwZywlpEhDpANOexxDhIoDvd-FihTiQLcZ93SCWjFTyAiFJk9nqAFjLfQ-1B2dlrGGeURa3Ig5lVAuyImHseDlMZ6Tu8-fbq-_djffv3y7_nDTOaVY7QR3fKOY8matpOGCD4MxbqXY0DsPymvvDVdr6SVo1f4AIDjARg6cr9E5J8_J-wN3XjYTDq7tlGG0cw4T5L1NEOy_lRh2dpt-2b5xNdMN8PYIyOnngqXaKRSH4wgR01Js-2tvtOn5o1QcpK6dWDL6pzGc2UeX7F-X7NGl1vTm-YJPLX88aYLuIEjL_D_A398IpSE</recordid><startdate>2022</startdate><enddate>2022</enddate><creator>van Wageningen, Thecla A.</creator><creator>Gerrits, Emma</creator><creator>Brouwer, Nieske</creator><creator>Brevé, John J. P.</creator><creator>Geurts, Jeroen J. G.</creator><creator>Eggen, Bart J. L.</creator><creator>Boddeke, H. W. G. M. (Erik)</creator><creator>van Dam, Anne-Marie</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-7248-8779</orcidid><orcidid>https://orcid.org/0000-0003-1896-3748</orcidid><orcidid>https://orcid.org/0000-0002-5304-9487</orcidid></search><sort><creationdate>2022</creationdate><title>Distinct gene expression in demyelinated white and grey matter areas of patients with multiple sclerosis</title><author>van Wageningen, Thecla A. ; Gerrits, Emma ; Brouwer, Nieske ; Brevé, John J. P. ; Geurts, Jeroen J. G. ; Eggen, Bart J. L. ; Boddeke, H. W. G. M. (Erik) ; van Dam, Anne-Marie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-21c1b404f97439121dd99c640d8cfa4f5ff91473f3a54093aa21aab3d117eccc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Original</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>van Wageningen, Thecla A.</creatorcontrib><creatorcontrib>Gerrits, Emma</creatorcontrib><creatorcontrib>Brouwer, Nieske</creatorcontrib><creatorcontrib>Brevé, John J. P.</creatorcontrib><creatorcontrib>Geurts, Jeroen J. G.</creatorcontrib><creatorcontrib>Eggen, Bart J. L.</creatorcontrib><creatorcontrib>Boddeke, H. W. G. M. (Erik)</creatorcontrib><creatorcontrib>van Dam, Anne-Marie</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Brain communications</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>van Wageningen, Thecla A.</au><au>Gerrits, Emma</au><au>Brouwer, Nieske</au><au>Brevé, John J. P.</au><au>Geurts, Jeroen J. G.</au><au>Eggen, Bart J. L.</au><au>Boddeke, H. W. G. M. (Erik)</au><au>van Dam, Anne-Marie</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Distinct gene expression in demyelinated white and grey matter areas of patients with multiple sclerosis</atitle><jtitle>Brain communications</jtitle><addtitle>Brain Commun</addtitle><date>2022</date><risdate>2022</risdate><volume>4</volume><issue>2</issue><spage>fcac005</spage><epage>fcac005</epage><pages>fcac005-fcac005</pages><issn>2632-1297</issn><eissn>2632-1297</eissn><abstract>Abstract Demyelination of the central nervous system is a prominent pathological hallmark of multiple sclerosis and affects both white and grey matter. However, demyelinated white and grey matter exhibit clear pathological differences, most notably the presence or absence of inflammation and activated glial cells in white and grey matter, respectively. In order to gain more insight into the differential pathology of demyelinated white and grey matter areas, we micro-dissected neighbouring white and grey matter demyelinated areas as well as normal-appearing matter from leucocortical lesions of human post-mortem material and used these samples for RNA sequencing. Our data show that even neighbouring demyelinated white and grey matter of the same leucocortical have a distinct gene expression profile and cellular composition. We propose that, based on their distinct expression profile, pathological processes in neighbouring white and grey matter are likely different which could have implications for the efficacy of treating grey matter lesions with current anti-inflammatory-based multiple sclerosis drugs. van Wageningen et al. present gene expression data of demyelinated and normal-appearing white and grey matter of multiple sclerosis leucocortical lesions. They find that grey matter lesions primarily feature gene expression indicative of a microglial response while white matter lesions feature astrocytic activation and dystrophic neurons. Graphical Abstract Graphical Abstract</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>35282162</pmid><doi>10.1093/braincomms/fcac005</doi><orcidid>https://orcid.org/0000-0001-7248-8779</orcidid><orcidid>https://orcid.org/0000-0003-1896-3748</orcidid><orcidid>https://orcid.org/0000-0002-5304-9487</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 2632-1297
ispartof Brain communications, 2022, Vol.4 (2), p.fcac005-fcac005
issn 2632-1297
2632-1297
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_8914505
source DOAJ Directory of Open Access Journals; Oxford Journals Open Access Collection; EZB-FREE-00999 freely available EZB journals; PubMed Central
subjects Original
title Distinct gene expression in demyelinated white and grey matter areas of patients with multiple sclerosis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T17%3A59%3A31IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Distinct%20gene%20expression%20in%20demyelinated%20white%20and%20grey%20matter%20areas%20of%20patients%20with%20multiple%20sclerosis&rft.jtitle=Brain%20communications&rft.au=van%20Wageningen,%20Thecla%20A.&rft.date=2022&rft.volume=4&rft.issue=2&rft.spage=fcac005&rft.epage=fcac005&rft.pages=fcac005-fcac005&rft.issn=2632-1297&rft.eissn=2632-1297&rft_id=info:doi/10.1093/braincomms/fcac005&rft_dat=%3Cproquest_pubme%3E2638959815%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2638959815&rft_id=info:pmid/35282162&rft_oup_id=10.1093/braincomms/fcac005&rfr_iscdi=true