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...
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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 |
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► 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> |
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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 |
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