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Protocol for the isolation and purification of human follicular dendritic cells for functional assays

In this protocol, we detail how to isolate and purify human follicular dendritic cells (FDCs) from lymphoid tissues. FDCs play a vital role in antibody development by presenting antigens to B cells in germinal centers. The assay involves enzymatic digestion and fluorescence-activated cell sorting an...

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Detalles Bibliográficos
Autores principales: Breeuwsma, Martijn, Heesters, Balthasar A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336301/
https://www.ncbi.nlm.nih.gov/pubmed/37392392
http://dx.doi.org/10.1016/j.xpro.2023.102404
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author Breeuwsma, Martijn
Heesters, Balthasar A.
author_facet Breeuwsma, Martijn
Heesters, Balthasar A.
author_sort Breeuwsma, Martijn
collection PubMed
description In this protocol, we detail how to isolate and purify human follicular dendritic cells (FDCs) from lymphoid tissues. FDCs play a vital role in antibody development by presenting antigens to B cells in germinal centers. The assay involves enzymatic digestion and fluorescence-activated cell sorting and is successfully applied to various lymphoid tissues, including tonsils, lymph nodes, and tertiary lymphoid structures. Our robust technique enables the isolation of FDCs and facilitates downstream functional and descriptive assays. For complete details on the use and execution of this protocol, please refer to Heesters et al.(1)
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spelling pubmed-103363012023-07-13 Protocol for the isolation and purification of human follicular dendritic cells for functional assays Breeuwsma, Martijn Heesters, Balthasar A. STAR Protoc Protocol In this protocol, we detail how to isolate and purify human follicular dendritic cells (FDCs) from lymphoid tissues. FDCs play a vital role in antibody development by presenting antigens to B cells in germinal centers. The assay involves enzymatic digestion and fluorescence-activated cell sorting and is successfully applied to various lymphoid tissues, including tonsils, lymph nodes, and tertiary lymphoid structures. Our robust technique enables the isolation of FDCs and facilitates downstream functional and descriptive assays. For complete details on the use and execution of this protocol, please refer to Heesters et al.(1) Elsevier 2023-06-30 /pmc/articles/PMC10336301/ /pubmed/37392392 http://dx.doi.org/10.1016/j.xpro.2023.102404 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Breeuwsma, Martijn
Heesters, Balthasar A.
Protocol for the isolation and purification of human follicular dendritic cells for functional assays
title Protocol for the isolation and purification of human follicular dendritic cells for functional assays
title_full Protocol for the isolation and purification of human follicular dendritic cells for functional assays
title_fullStr Protocol for the isolation and purification of human follicular dendritic cells for functional assays
title_full_unstemmed Protocol for the isolation and purification of human follicular dendritic cells for functional assays
title_short Protocol for the isolation and purification of human follicular dendritic cells for functional assays
title_sort protocol for the isolation and purification of human follicular dendritic cells for functional assays
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336301/
https://www.ncbi.nlm.nih.gov/pubmed/37392392
http://dx.doi.org/10.1016/j.xpro.2023.102404
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