The blood–brain barrier, chemokines and multiple sclerosis

The infiltration of leukocytes into the central nervous system (CNS) is an essential step in the neuropathogenesis of multiple sclerosis (MS). Leukocyte extravasation from the bloodstream is a multistep process that depends on several factors including fluid dynamics within the vasculature and molec...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Biochimica et biophysica acta 2011-02, Vol.1812 (2), p.220-230
Hauptverfasser: Holman, David W., Klein, Robyn S., Ransohoff, Richard M.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 230
container_issue 2
container_start_page 220
container_title Biochimica et biophysica acta
container_volume 1812
creator Holman, David W.
Klein, Robyn S.
Ransohoff, Richard M.
description The infiltration of leukocytes into the central nervous system (CNS) is an essential step in the neuropathogenesis of multiple sclerosis (MS). Leukocyte extravasation from the bloodstream is a multistep process that depends on several factors including fluid dynamics within the vasculature and molecular interactions between circulating leukocytes and the vascular endothelium. An important step in this cascade is the presence of chemokines on the vascular endothelial cell surface. Chemokines displayed along the endothelial lumen bind chemokine receptors on circulating leukocytes, initiating intracellular signaling that culminates in integrin activation, leukocyte arrest, and extravasation. The presence of chemokines at the endothelial lumen can help guide the movement of leukocytes through peripheral tissues during normal immune surveillance, host defense or inflammation. The expression and display of homeostatic or inflammatory chemokines therefore critically determine which leukocyte subsets extravasate and enter the peripheral tissues. Within the CNS, however, infiltrating leukocytes that cross the endothelium face additional boundaries to parenchymal entry, including the abluminal presence of localizing cues that prevent egress from perivascular spaces. This review focuses on the differential display of chemokines along endothelial surfaces and how they impact leukocyte extravasation into parenchymal tissues, especially within the CNS. In particular, the display of chemokines by endothelial cells of the blood brain barrier may be altered during CNS autoimmune disease, promoting leukocyte entry into this immunologically distinct site. Recent advances in microscopic techniques, including two-photon and intravital imaging have provided new insights into the mechanisms of chemokine-mediated capture of leukocytes within the CNS. ► Leukocyte extravasation from the bloodstream into peripheral tissues is a multistep process. ► Chemokines displayed along endothelial surfaces provide guiding cues to circulating leukocytes and intiate intracellular signalling cascades. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations.
doi_str_mv 10.1016/j.bbadis.2010.07.019
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_hal_primary_oai_HAL_hal_00652656v1</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0925443910001560</els_id><sourcerecordid>820784930</sourcerecordid><originalsourceid>FETCH-LOGICAL-c562t-5e5cb1a4ab5dc2ce64e58607878bec2463d2396ed0f3a14e92eaf703824d7aac3</originalsourceid><addsrcrecordid>eNp9kd9qFDEUxoModlt9A5G5E6GznvydGShCKdoKC95U8C7kz1k325nJNpld8M538A37JGbZWqsX5iZw8p3v5Hw_Ql5RmFOg6t16bq3xIc8ZlBI0c6DdEzKjbdPVTMHXp2QGHZO1ELw7Isc5r6Ec1cBzcsRAdYzzdkbOrldY2T5Gf_fjp00mjJU1KQVMp5Vb4RBvwoi5MqOvhm0_hU2PVXY9pphDfkGeLU2f8eX9fUK-fPxwfXFVLz5ffro4X9ROKjbVEqWz1AhjpXfMoRIoWwVN27QWHROKe8Y7hR6W3FCBHUOzbIC3TPjGGMdPyPuD72ZrB_QOxymZXm9SGEz6rqMJ-u-XMaz0t7jTHEBSYMXg7cFg9U_b1flC72slGMmUVDtatG_uh6V4u8U86SFkh31vRozbrFtWfi46DkUpDkpX0sgJlw_WFPSekV7rAyO9Z6Sh0YVRaXv9eJuHpt9Q_qyLJdNdQaGzCzg69CGhm7SP4f8TfgGVX6XP</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>820784930</pqid></control><display><type>article</type><title>The blood–brain barrier, chemokines and multiple sclerosis</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals Complete</source><source>Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals</source><creator>Holman, David W. ; Klein, Robyn S. ; Ransohoff, Richard M.</creator><creatorcontrib>Holman, David W. ; Klein, Robyn S. ; Ransohoff, Richard M.</creatorcontrib><description>The infiltration of leukocytes into the central nervous system (CNS) is an essential step in the neuropathogenesis of multiple sclerosis (MS). Leukocyte extravasation from the bloodstream is a multistep process that depends on several factors including fluid dynamics within the vasculature and molecular interactions between circulating leukocytes and the vascular endothelium. An important step in this cascade is the presence of chemokines on the vascular endothelial cell surface. Chemokines displayed along the endothelial lumen bind chemokine receptors on circulating leukocytes, initiating intracellular signaling that culminates in integrin activation, leukocyte arrest, and extravasation. The presence of chemokines at the endothelial lumen can help guide the movement of leukocytes through peripheral tissues during normal immune surveillance, host defense or inflammation. The expression and display of homeostatic or inflammatory chemokines therefore critically determine which leukocyte subsets extravasate and enter the peripheral tissues. Within the CNS, however, infiltrating leukocytes that cross the endothelium face additional boundaries to parenchymal entry, including the abluminal presence of localizing cues that prevent egress from perivascular spaces. This review focuses on the differential display of chemokines along endothelial surfaces and how they impact leukocyte extravasation into parenchymal tissues, especially within the CNS. In particular, the display of chemokines by endothelial cells of the blood brain barrier may be altered during CNS autoimmune disease, promoting leukocyte entry into this immunologically distinct site. Recent advances in microscopic techniques, including two-photon and intravital imaging have provided new insights into the mechanisms of chemokine-mediated capture of leukocytes within the CNS. ► Leukocyte extravasation from the bloodstream into peripheral tissues is a multistep process. ► Chemokines displayed along endothelial surfaces provide guiding cues to circulating leukocytes and intiate intracellular signalling cascades. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations.</description><identifier>ISSN: 0925-4439</identifier><identifier>ISSN: 0006-3002</identifier><identifier>EISSN: 1879-260X</identifier><identifier>DOI: 10.1016/j.bbadis.2010.07.019</identifier><identifier>PMID: 20692338</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Animals ; Blood-Brain Barrier - immunology ; Blood-Brain Barrier - physiology ; Blood–brain barrier ; Cell Movement ; Chemokine ; Chemokines - immunology ; Chemokines - physiology ; Endothelium - immunology ; Endothelium - physiology ; Humans ; Immunity, Innate ; Inflammation ; Leukocyte ; Leukocytes - immunology ; Leukocytes - physiology ; Lymphoid Tissue - immunology ; Lymphoid Tissue - physiology ; Models, Immunological ; Models, Neurological ; Multiple Sclerosis - etiology ; Multiple Sclerosis - immunology ; Receptors, Chemokine - immunology ; Receptors, Chemokine - physiology</subject><ispartof>Biochimica et biophysica acta, 2011-02, Vol.1812 (2), p.220-230</ispartof><rights>2010 Elsevier B.V.</rights><rights>2010 Elsevier B.V. All rights reserved.</rights><rights>Distributed under a Creative Commons Attribution 4.0 International License</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c562t-5e5cb1a4ab5dc2ce64e58607878bec2463d2396ed0f3a14e92eaf703824d7aac3</citedby><cites>FETCH-LOGICAL-c562t-5e5cb1a4ab5dc2ce64e58607878bec2463d2396ed0f3a14e92eaf703824d7aac3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.bbadis.2010.07.019$$EHTML$$P50$$Gelsevier$$Hfree_for_read</linktohtml><link.rule.ids>230,314,780,784,885,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/20692338$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttps://hal.science/hal-00652656$$DView record in HAL$$Hfree_for_read</backlink></links><search><creatorcontrib>Holman, David W.</creatorcontrib><creatorcontrib>Klein, Robyn S.</creatorcontrib><creatorcontrib>Ransohoff, Richard M.</creatorcontrib><title>The blood–brain barrier, chemokines and multiple sclerosis</title><title>Biochimica et biophysica acta</title><addtitle>Biochim Biophys Acta</addtitle><description>The infiltration of leukocytes into the central nervous system (CNS) is an essential step in the neuropathogenesis of multiple sclerosis (MS). Leukocyte extravasation from the bloodstream is a multistep process that depends on several factors including fluid dynamics within the vasculature and molecular interactions between circulating leukocytes and the vascular endothelium. An important step in this cascade is the presence of chemokines on the vascular endothelial cell surface. Chemokines displayed along the endothelial lumen bind chemokine receptors on circulating leukocytes, initiating intracellular signaling that culminates in integrin activation, leukocyte arrest, and extravasation. The presence of chemokines at the endothelial lumen can help guide the movement of leukocytes through peripheral tissues during normal immune surveillance, host defense or inflammation. The expression and display of homeostatic or inflammatory chemokines therefore critically determine which leukocyte subsets extravasate and enter the peripheral tissues. Within the CNS, however, infiltrating leukocytes that cross the endothelium face additional boundaries to parenchymal entry, including the abluminal presence of localizing cues that prevent egress from perivascular spaces. This review focuses on the differential display of chemokines along endothelial surfaces and how they impact leukocyte extravasation into parenchymal tissues, especially within the CNS. In particular, the display of chemokines by endothelial cells of the blood brain barrier may be altered during CNS autoimmune disease, promoting leukocyte entry into this immunologically distinct site. Recent advances in microscopic techniques, including two-photon and intravital imaging have provided new insights into the mechanisms of chemokine-mediated capture of leukocytes within the CNS. ► Leukocyte extravasation from the bloodstream into peripheral tissues is a multistep process. ► Chemokines displayed along endothelial surfaces provide guiding cues to circulating leukocytes and intiate intracellular signalling cascades. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations.</description><subject>Animals</subject><subject>Blood-Brain Barrier - immunology</subject><subject>Blood-Brain Barrier - physiology</subject><subject>Blood–brain barrier</subject><subject>Cell Movement</subject><subject>Chemokine</subject><subject>Chemokines - immunology</subject><subject>Chemokines - physiology</subject><subject>Endothelium - immunology</subject><subject>Endothelium - physiology</subject><subject>Humans</subject><subject>Immunity, Innate</subject><subject>Inflammation</subject><subject>Leukocyte</subject><subject>Leukocytes - immunology</subject><subject>Leukocytes - physiology</subject><subject>Lymphoid Tissue - immunology</subject><subject>Lymphoid Tissue - physiology</subject><subject>Models, Immunological</subject><subject>Models, Neurological</subject><subject>Multiple Sclerosis - etiology</subject><subject>Multiple Sclerosis - immunology</subject><subject>Receptors, Chemokine - immunology</subject><subject>Receptors, Chemokine - physiology</subject><issn>0925-4439</issn><issn>0006-3002</issn><issn>1879-260X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kd9qFDEUxoModlt9A5G5E6GznvydGShCKdoKC95U8C7kz1k325nJNpld8M538A37JGbZWqsX5iZw8p3v5Hw_Ql5RmFOg6t16bq3xIc8ZlBI0c6DdEzKjbdPVTMHXp2QGHZO1ELw7Isc5r6Ec1cBzcsRAdYzzdkbOrldY2T5Gf_fjp00mjJU1KQVMp5Vb4RBvwoi5MqOvhm0_hU2PVXY9pphDfkGeLU2f8eX9fUK-fPxwfXFVLz5ffro4X9ROKjbVEqWz1AhjpXfMoRIoWwVN27QWHROKe8Y7hR6W3FCBHUOzbIC3TPjGGMdPyPuD72ZrB_QOxymZXm9SGEz6rqMJ-u-XMaz0t7jTHEBSYMXg7cFg9U_b1flC72slGMmUVDtatG_uh6V4u8U86SFkh31vRozbrFtWfi46DkUpDkpX0sgJlw_WFPSekV7rAyO9Z6Sh0YVRaXv9eJuHpt9Q_qyLJdNdQaGzCzg69CGhm7SP4f8TfgGVX6XP</recordid><startdate>20110201</startdate><enddate>20110201</enddate><creator>Holman, David W.</creator><creator>Klein, Robyn S.</creator><creator>Ransohoff, Richard M.</creator><general>Elsevier B.V</general><general>Elsevier</general><scope>6I.</scope><scope>AAFTH</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>7X8</scope><scope>1XC</scope><scope>VOOES</scope><scope>5PM</scope></search><sort><creationdate>20110201</creationdate><title>The blood–brain barrier, chemokines and multiple sclerosis</title><author>Holman, David W. ; Klein, Robyn S. ; Ransohoff, Richard M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c562t-5e5cb1a4ab5dc2ce64e58607878bec2463d2396ed0f3a14e92eaf703824d7aac3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Animals</topic><topic>Blood-Brain Barrier - immunology</topic><topic>Blood-Brain Barrier - physiology</topic><topic>Blood–brain barrier</topic><topic>Cell Movement</topic><topic>Chemokine</topic><topic>Chemokines - immunology</topic><topic>Chemokines - physiology</topic><topic>Endothelium - immunology</topic><topic>Endothelium - physiology</topic><topic>Humans</topic><topic>Immunity, Innate</topic><topic>Inflammation</topic><topic>Leukocyte</topic><topic>Leukocytes - immunology</topic><topic>Leukocytes - physiology</topic><topic>Lymphoid Tissue - immunology</topic><topic>Lymphoid Tissue - physiology</topic><topic>Models, Immunological</topic><topic>Models, Neurological</topic><topic>Multiple Sclerosis - etiology</topic><topic>Multiple Sclerosis - immunology</topic><topic>Receptors, Chemokine - immunology</topic><topic>Receptors, Chemokine - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Holman, David W.</creatorcontrib><creatorcontrib>Klein, Robyn S.</creatorcontrib><creatorcontrib>Ransohoff, Richard M.</creatorcontrib><collection>ScienceDirect Open Access Titles</collection><collection>Elsevier:ScienceDirect:Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Hyper Article en Ligne (HAL)</collection><collection>Hyper Article en Ligne (HAL) (Open Access)</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Biochimica et biophysica acta</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Holman, David W.</au><au>Klein, Robyn S.</au><au>Ransohoff, Richard M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The blood–brain barrier, chemokines and multiple sclerosis</atitle><jtitle>Biochimica et biophysica acta</jtitle><addtitle>Biochim Biophys Acta</addtitle><date>2011-02-01</date><risdate>2011</risdate><volume>1812</volume><issue>2</issue><spage>220</spage><epage>230</epage><pages>220-230</pages><issn>0925-4439</issn><issn>0006-3002</issn><eissn>1879-260X</eissn><abstract>The infiltration of leukocytes into the central nervous system (CNS) is an essential step in the neuropathogenesis of multiple sclerosis (MS). Leukocyte extravasation from the bloodstream is a multistep process that depends on several factors including fluid dynamics within the vasculature and molecular interactions between circulating leukocytes and the vascular endothelium. An important step in this cascade is the presence of chemokines on the vascular endothelial cell surface. Chemokines displayed along the endothelial lumen bind chemokine receptors on circulating leukocytes, initiating intracellular signaling that culminates in integrin activation, leukocyte arrest, and extravasation. The presence of chemokines at the endothelial lumen can help guide the movement of leukocytes through peripheral tissues during normal immune surveillance, host defense or inflammation. The expression and display of homeostatic or inflammatory chemokines therefore critically determine which leukocyte subsets extravasate and enter the peripheral tissues. Within the CNS, however, infiltrating leukocytes that cross the endothelium face additional boundaries to parenchymal entry, including the abluminal presence of localizing cues that prevent egress from perivascular spaces. This review focuses on the differential display of chemokines along endothelial surfaces and how they impact leukocyte extravasation into parenchymal tissues, especially within the CNS. In particular, the display of chemokines by endothelial cells of the blood brain barrier may be altered during CNS autoimmune disease, promoting leukocyte entry into this immunologically distinct site. Recent advances in microscopic techniques, including two-photon and intravital imaging have provided new insights into the mechanisms of chemokine-mediated capture of leukocytes within the CNS. ► Leukocyte extravasation from the bloodstream into peripheral tissues is a multistep process. ► Chemokines displayed along endothelial surfaces provide guiding cues to circulating leukocytes and intiate intracellular signalling cascades. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations. ► The central nervous system is considered an immunologically specialized site and leukocyte trafficking is tightly regulated by anatomical and biochemical specializations.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>20692338</pmid><doi>10.1016/j.bbadis.2010.07.019</doi><tpages>11</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0925-4439
ispartof Biochimica et biophysica acta, 2011-02, Vol.1812 (2), p.220-230
issn 0925-4439
0006-3002
1879-260X
language eng
recordid cdi_hal_primary_oai_HAL_hal_00652656v1
source MEDLINE; Elsevier ScienceDirect Journals Complete; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals
subjects Animals
Blood-Brain Barrier - immunology
Blood-Brain Barrier - physiology
Blood–brain barrier
Cell Movement
Chemokine
Chemokines - immunology
Chemokines - physiology
Endothelium - immunology
Endothelium - physiology
Humans
Immunity, Innate
Inflammation
Leukocyte
Leukocytes - immunology
Leukocytes - physiology
Lymphoid Tissue - immunology
Lymphoid Tissue - physiology
Models, Immunological
Models, Neurological
Multiple Sclerosis - etiology
Multiple Sclerosis - immunology
Receptors, Chemokine - immunology
Receptors, Chemokine - physiology
title The blood–brain barrier, chemokines and multiple sclerosis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-05T07%3A06%3A05IST&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=The%20blood%E2%80%93brain%20barrier,%20chemokines%20and%20multiple%20sclerosis&rft.jtitle=Biochimica%20et%20biophysica%20acta&rft.au=Holman,%20David%20W.&rft.date=2011-02-01&rft.volume=1812&rft.issue=2&rft.spage=220&rft.epage=230&rft.pages=220-230&rft.issn=0925-4439&rft.eissn=1879-260X&rft_id=info:doi/10.1016/j.bbadis.2010.07.019&rft_dat=%3Cproquest_pubme%3E820784930%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=820784930&rft_id=info:pmid/20692338&rft_els_id=S0925443910001560&rfr_iscdi=true