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Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies
Tertiary lymphoid structures (TLS) are organized aggregates of B and T cells formed ectopically during different stages of life in response to inflammation, infection, or cancer. Here, we describe formation of structures reminiscent of TLS in the spinal cord meninges under several central nervous sy...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723261/ https://www.ncbi.nlm.nih.gov/pubmed/33277355 http://dx.doi.org/10.26508/lsa.202000907 |
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author | Cohen, Merav Giladi, Amir Raposo, Catarina Zada, Mor Li, Baoguo Ruckh, Julia Deczkowska, Aleksandra Mohar, Boaz Shechter, Ravid Lichtenstein, Rachel G Amit, Ido Schwartz, Michal |
author_facet | Cohen, Merav Giladi, Amir Raposo, Catarina Zada, Mor Li, Baoguo Ruckh, Julia Deczkowska, Aleksandra Mohar, Boaz Shechter, Ravid Lichtenstein, Rachel G Amit, Ido Schwartz, Michal |
author_sort | Cohen, Merav |
collection | PubMed |
description | Tertiary lymphoid structures (TLS) are organized aggregates of B and T cells formed ectopically during different stages of life in response to inflammation, infection, or cancer. Here, we describe formation of structures reminiscent of TLS in the spinal cord meninges under several central nervous system (CNS) pathologies. After acute spinal cord injury, B and T lymphocytes locally aggregate within the meninges to form TLS-like structures, and continue to accumulate during the late phase of the response to the injury, with a negative impact on subsequent pathological conditions, such as experimental autoimmune encephalomyelitis. Using a chronic model of spinal cord pathology, the mSOD1 mouse model of amyotrophic lateral sclerosis, we further showed by single-cell RNA-sequencing that a meningeal lymphocyte niche forms, with a unique organization and activation state, including accumulation of pre-B cells in the spinal cord meninges. Such a response was not found in the CNS-draining cervical lymph nodes. The present findings suggest that a special immune response develops in the meninges during various neurological pathologies in the CNS, a possible reflection of its immune privileged nature. |
format | Online Article Text |
id | pubmed-7723261 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-77232612020-12-21 Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies Cohen, Merav Giladi, Amir Raposo, Catarina Zada, Mor Li, Baoguo Ruckh, Julia Deczkowska, Aleksandra Mohar, Boaz Shechter, Ravid Lichtenstein, Rachel G Amit, Ido Schwartz, Michal Life Sci Alliance Research Articles Tertiary lymphoid structures (TLS) are organized aggregates of B and T cells formed ectopically during different stages of life in response to inflammation, infection, or cancer. Here, we describe formation of structures reminiscent of TLS in the spinal cord meninges under several central nervous system (CNS) pathologies. After acute spinal cord injury, B and T lymphocytes locally aggregate within the meninges to form TLS-like structures, and continue to accumulate during the late phase of the response to the injury, with a negative impact on subsequent pathological conditions, such as experimental autoimmune encephalomyelitis. Using a chronic model of spinal cord pathology, the mSOD1 mouse model of amyotrophic lateral sclerosis, we further showed by single-cell RNA-sequencing that a meningeal lymphocyte niche forms, with a unique organization and activation state, including accumulation of pre-B cells in the spinal cord meninges. Such a response was not found in the CNS-draining cervical lymph nodes. The present findings suggest that a special immune response develops in the meninges during various neurological pathologies in the CNS, a possible reflection of its immune privileged nature. Life Science Alliance LLC 2020-12-04 /pmc/articles/PMC7723261/ /pubmed/33277355 http://dx.doi.org/10.26508/lsa.202000907 Text en © 2020 Cohen et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Research Articles Cohen, Merav Giladi, Amir Raposo, Catarina Zada, Mor Li, Baoguo Ruckh, Julia Deczkowska, Aleksandra Mohar, Boaz Shechter, Ravid Lichtenstein, Rachel G Amit, Ido Schwartz, Michal Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies |
title | Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies |
title_full | Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies |
title_fullStr | Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies |
title_full_unstemmed | Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies |
title_short | Meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies |
title_sort | meningeal lymphoid structures are activated under acute and chronic spinal cord pathologies |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7723261/ https://www.ncbi.nlm.nih.gov/pubmed/33277355 http://dx.doi.org/10.26508/lsa.202000907 |
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