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CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells
Follicular dendritic cells (FDCs) are a specialized type of stromal cells that exclusively reside in B‐cell follicles. When inflammation occurs, the FDC network is reorganized to support germinal center (GC) polarization into the light zone (LZ) and dark zone (DZ). Despite the indispensable role of...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804338/ https://www.ncbi.nlm.nih.gov/pubmed/35907260 http://dx.doi.org/10.1002/eji.202249879 |
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author | Chen, Xin Zheng, Yuhan Liu, Siming Yu, Wenjing Liu, Zhiduo |
author_facet | Chen, Xin Zheng, Yuhan Liu, Siming Yu, Wenjing Liu, Zhiduo |
author_sort | Chen, Xin |
collection | PubMed |
description | Follicular dendritic cells (FDCs) are a specialized type of stromal cells that exclusively reside in B‐cell follicles. When inflammation occurs, the FDC network is reorganized to support germinal center (GC) polarization into the light zone (LZ) and dark zone (DZ). Despite the indispensable role of FDCs in supporting humoral responses, the FDC regulatory requirements remain incompletely defined. In this study, we unexpectedly observed an accumulation of CD169(+) subcapsular sinus macrophage (SSM)‐derived microvesicles (MVs) in the B‐cell zone, which were tightly associated with the FDC network. Interestingly, a selective deposition of CD169(+) MVs was detected in both GC LZ FDCs in secondary follicles and on predetermined LZ FDCs in primary follicles. The ablation of CD169(+) MVs, resulting from SSM depletion, resulted in significantly decreased expression of LZ‐related genes in FDCs. In addition, we found that CD169(+) MVs could colocalize with fluorescently tagged antigen‐containing immune complexes (ICs), supporting a possible role of CD169(+) MVs in transporting antigens to the FDC network. Thus, our data reveal intimate crosstalk between FDCs and SSMs located outside B‐cell follicles via SSM‐released MVs, providing a novel perspective on the mechanisms underlying the regulation of FDC maturation and polarization. |
format | Online Article Text |
id | pubmed-9804338 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98043382023-01-03 CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells Chen, Xin Zheng, Yuhan Liu, Siming Yu, Wenjing Liu, Zhiduo Eur J Immunol Tissue immunology and leukocyte trafficking Follicular dendritic cells (FDCs) are a specialized type of stromal cells that exclusively reside in B‐cell follicles. When inflammation occurs, the FDC network is reorganized to support germinal center (GC) polarization into the light zone (LZ) and dark zone (DZ). Despite the indispensable role of FDCs in supporting humoral responses, the FDC regulatory requirements remain incompletely defined. In this study, we unexpectedly observed an accumulation of CD169(+) subcapsular sinus macrophage (SSM)‐derived microvesicles (MVs) in the B‐cell zone, which were tightly associated with the FDC network. Interestingly, a selective deposition of CD169(+) MVs was detected in both GC LZ FDCs in secondary follicles and on predetermined LZ FDCs in primary follicles. The ablation of CD169(+) MVs, resulting from SSM depletion, resulted in significantly decreased expression of LZ‐related genes in FDCs. In addition, we found that CD169(+) MVs could colocalize with fluorescently tagged antigen‐containing immune complexes (ICs), supporting a possible role of CD169(+) MVs in transporting antigens to the FDC network. Thus, our data reveal intimate crosstalk between FDCs and SSMs located outside B‐cell follicles via SSM‐released MVs, providing a novel perspective on the mechanisms underlying the regulation of FDC maturation and polarization. John Wiley and Sons Inc. 2022-08-10 2022-10 /pmc/articles/PMC9804338/ /pubmed/35907260 http://dx.doi.org/10.1002/eji.202249879 Text en © 2022 The Authors. European Journal of Immunology published by Wiley‐VCH GmbH https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Tissue immunology and leukocyte trafficking Chen, Xin Zheng, Yuhan Liu, Siming Yu, Wenjing Liu, Zhiduo CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells |
title | CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells |
title_full | CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells |
title_fullStr | CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells |
title_full_unstemmed | CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells |
title_short | CD169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells |
title_sort | cd169(+) subcapsular sinus macrophage‐derived microvesicles are associated with light zone follicular dendritic cells |
topic | Tissue immunology and leukocyte trafficking |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9804338/ https://www.ncbi.nlm.nih.gov/pubmed/35907260 http://dx.doi.org/10.1002/eji.202249879 |
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