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Vascular, glial, and lymphatic immune gateways of the central nervous system

Immune privilege of the central nervous system (CNS) has been ascribed to the presence of a blood–brain barrier and the lack of lymphatic vessels within the CNS parenchyma. However, immune reactions occur within the CNS and it is clear that the CNS has a unique relationship with the immune system. R...

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Autores principales: Engelhardt, Britta, Carare, Roxana O., Bechmann, Ingo, Flügel, Alexander, Laman, Jon D., Weller, Roy O.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992028/
https://www.ncbi.nlm.nih.gov/pubmed/27522506
http://dx.doi.org/10.1007/s00401-016-1606-5
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author Engelhardt, Britta
Carare, Roxana O.
Bechmann, Ingo
Flügel, Alexander
Laman, Jon D.
Weller, Roy O.
author_facet Engelhardt, Britta
Carare, Roxana O.
Bechmann, Ingo
Flügel, Alexander
Laman, Jon D.
Weller, Roy O.
author_sort Engelhardt, Britta
collection PubMed
description Immune privilege of the central nervous system (CNS) has been ascribed to the presence of a blood–brain barrier and the lack of lymphatic vessels within the CNS parenchyma. However, immune reactions occur within the CNS and it is clear that the CNS has a unique relationship with the immune system. Recent developments in high-resolution imaging techniques have prompted a reassessment of the relationships between the CNS and the immune system. This review will take these developments into account in describing our present understanding of the anatomical connections of the CNS fluid drainage pathways towards regional lymph nodes and our current concept of immune cell trafficking into the CNS during immunosurveillance and neuroinflammation. Cerebrospinal fluid (CSF) and interstitial fluid are the two major components that drain from the CNS to regional lymph nodes. CSF drains via lymphatic vessels and appears to carry antigen-presenting cells. Interstitial fluid from the CNS parenchyma, on the other hand, drains to lymph nodes via narrow and restricted basement membrane pathways within the walls of cerebral capillaries and arteries that do not allow traffic of antigen-presenting cells. Lymphocytes targeting the CNS enter by a two-step process entailing receptor-mediated crossing of vascular endothelium and enzyme-mediated penetration of the glia limitans that covers the CNS. The contribution of the pathways into and out of the CNS as initiators or contributors to neurological disorders, such as multiple sclerosis and Alzheimer’s disease, will be discussed. Furthermore, we propose a clear nomenclature allowing improved precision when describing the CNS-specific communication pathways with the immune system.
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spelling pubmed-49920282016-09-06 Vascular, glial, and lymphatic immune gateways of the central nervous system Engelhardt, Britta Carare, Roxana O. Bechmann, Ingo Flügel, Alexander Laman, Jon D. Weller, Roy O. Acta Neuropathol Review Immune privilege of the central nervous system (CNS) has been ascribed to the presence of a blood–brain barrier and the lack of lymphatic vessels within the CNS parenchyma. However, immune reactions occur within the CNS and it is clear that the CNS has a unique relationship with the immune system. Recent developments in high-resolution imaging techniques have prompted a reassessment of the relationships between the CNS and the immune system. This review will take these developments into account in describing our present understanding of the anatomical connections of the CNS fluid drainage pathways towards regional lymph nodes and our current concept of immune cell trafficking into the CNS during immunosurveillance and neuroinflammation. Cerebrospinal fluid (CSF) and interstitial fluid are the two major components that drain from the CNS to regional lymph nodes. CSF drains via lymphatic vessels and appears to carry antigen-presenting cells. Interstitial fluid from the CNS parenchyma, on the other hand, drains to lymph nodes via narrow and restricted basement membrane pathways within the walls of cerebral capillaries and arteries that do not allow traffic of antigen-presenting cells. Lymphocytes targeting the CNS enter by a two-step process entailing receptor-mediated crossing of vascular endothelium and enzyme-mediated penetration of the glia limitans that covers the CNS. The contribution of the pathways into and out of the CNS as initiators or contributors to neurological disorders, such as multiple sclerosis and Alzheimer’s disease, will be discussed. Furthermore, we propose a clear nomenclature allowing improved precision when describing the CNS-specific communication pathways with the immune system. Springer Berlin Heidelberg 2016-08-13 2016 /pmc/articles/PMC4992028/ /pubmed/27522506 http://dx.doi.org/10.1007/s00401-016-1606-5 Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Review
Engelhardt, Britta
Carare, Roxana O.
Bechmann, Ingo
Flügel, Alexander
Laman, Jon D.
Weller, Roy O.
Vascular, glial, and lymphatic immune gateways of the central nervous system
title Vascular, glial, and lymphatic immune gateways of the central nervous system
title_full Vascular, glial, and lymphatic immune gateways of the central nervous system
title_fullStr Vascular, glial, and lymphatic immune gateways of the central nervous system
title_full_unstemmed Vascular, glial, and lymphatic immune gateways of the central nervous system
title_short Vascular, glial, and lymphatic immune gateways of the central nervous system
title_sort vascular, glial, and lymphatic immune gateways of the central nervous system
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4992028/
https://www.ncbi.nlm.nih.gov/pubmed/27522506
http://dx.doi.org/10.1007/s00401-016-1606-5
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