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Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage
Extravasated erythrocytes in cerebrospinal fluid (CSF) critically contribute to the pathogenesis of subarachnoid hemorrhage (SAH). Meningeal lymphatics have been reported to drain macromolecules and immune cells from CSF into cervical lymph nodes (CLNs). However, whether meningeal lymphatics are inv...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308412/ https://www.ncbi.nlm.nih.gov/pubmed/32572022 http://dx.doi.org/10.1038/s41467-020-16851-z |
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author | Chen, Jinman Wang, Linmei Xu, Hao Xing, Lianping Zhuang, Zixin Zheng, Yangkang Li, Xuefei Wang, Chinyun Chen, Shaohua Guo, Zibin Liang, Qianqian Wang, Yongjun |
author_facet | Chen, Jinman Wang, Linmei Xu, Hao Xing, Lianping Zhuang, Zixin Zheng, Yangkang Li, Xuefei Wang, Chinyun Chen, Shaohua Guo, Zibin Liang, Qianqian Wang, Yongjun |
author_sort | Chen, Jinman |
collection | PubMed |
description | Extravasated erythrocytes in cerebrospinal fluid (CSF) critically contribute to the pathogenesis of subarachnoid hemorrhage (SAH). Meningeal lymphatics have been reported to drain macromolecules and immune cells from CSF into cervical lymph nodes (CLNs). However, whether meningeal lymphatics are involved in clearing extravasated erythrocytes in CSF after SAH remains unclear. Here we show that a markedly higher number of erythrocytes are accumulated in the lymphatics of CLNs and meningeal lymphatics after SAH. When the meningeal lymphatics are depleted in a mouse model of SAH, the degree of erythrocyte aggregation in CLNs is significantly lower, while the associated neuroinflammation and the neurologic deficits are dramatically exacerbated. In addition, during SAH lymph flow is increased but without significant lymphangiogenesis and lymphangiectasia. Taken together, this work demonstrates that the meningeal lymphatics drain extravasated erythrocytes from CSF into CLNs after SAH, while suggesting that modulating this draining may offer therapeutic approaches to alleviate SAH severity. |
format | Online Article Text |
id | pubmed-7308412 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-73084122020-06-26 Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage Chen, Jinman Wang, Linmei Xu, Hao Xing, Lianping Zhuang, Zixin Zheng, Yangkang Li, Xuefei Wang, Chinyun Chen, Shaohua Guo, Zibin Liang, Qianqian Wang, Yongjun Nat Commun Article Extravasated erythrocytes in cerebrospinal fluid (CSF) critically contribute to the pathogenesis of subarachnoid hemorrhage (SAH). Meningeal lymphatics have been reported to drain macromolecules and immune cells from CSF into cervical lymph nodes (CLNs). However, whether meningeal lymphatics are involved in clearing extravasated erythrocytes in CSF after SAH remains unclear. Here we show that a markedly higher number of erythrocytes are accumulated in the lymphatics of CLNs and meningeal lymphatics after SAH. When the meningeal lymphatics are depleted in a mouse model of SAH, the degree of erythrocyte aggregation in CLNs is significantly lower, while the associated neuroinflammation and the neurologic deficits are dramatically exacerbated. In addition, during SAH lymph flow is increased but without significant lymphangiogenesis and lymphangiectasia. Taken together, this work demonstrates that the meningeal lymphatics drain extravasated erythrocytes from CSF into CLNs after SAH, while suggesting that modulating this draining may offer therapeutic approaches to alleviate SAH severity. Nature Publishing Group UK 2020-06-22 /pmc/articles/PMC7308412/ /pubmed/32572022 http://dx.doi.org/10.1038/s41467-020-16851-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Chen, Jinman Wang, Linmei Xu, Hao Xing, Lianping Zhuang, Zixin Zheng, Yangkang Li, Xuefei Wang, Chinyun Chen, Shaohua Guo, Zibin Liang, Qianqian Wang, Yongjun Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage |
title | Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage |
title_full | Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage |
title_fullStr | Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage |
title_full_unstemmed | Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage |
title_short | Meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage |
title_sort | meningeal lymphatics clear erythrocytes that arise from subarachnoid hemorrhage |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7308412/ https://www.ncbi.nlm.nih.gov/pubmed/32572022 http://dx.doi.org/10.1038/s41467-020-16851-z |
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