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Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes

Conventional dendritic cells (cDCs) are divided into the following different subtypes: cDC1, which promotes a Th1 response, and cDC2, which stimulates a Th2 and Th17 response. These cells have not been characterized in porcine lymphoid tissues. DEC205 is a receptor that increases antigen presentatio...

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Autores principales: Parra-Sánchez, Héctor, Puebla-Clark, Lucinda, Reséndiz, Mónica, Valenzuela, Olivia, Hernández, Jesús
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112646/
https://www.ncbi.nlm.nih.gov/pubmed/29433077
http://dx.doi.org/10.1016/j.molimm.2018.02.003
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author Parra-Sánchez, Héctor
Puebla-Clark, Lucinda
Reséndiz, Mónica
Valenzuela, Olivia
Hernández, Jesús
author_facet Parra-Sánchez, Héctor
Puebla-Clark, Lucinda
Reséndiz, Mónica
Valenzuela, Olivia
Hernández, Jesús
author_sort Parra-Sánchez, Héctor
collection PubMed
description Conventional dendritic cells (cDCs) are divided into the following different subtypes: cDC1, which promotes a Th1 response, and cDC2, which stimulates a Th2 and Th17 response. These cells have not been characterized in porcine lymphoid tissues. DEC205 is a receptor that increases antigen presentation and allows DCs to cross-present antigens. The objectives of this work were to characterize cDCs subsets in the tonsil, submaxillary and mesenteric lymph nodes and spleen lymphoid tissues and to determine their expression of DEC205 by flow cytometry. The cDC1 (MHCII(high)CADM1(high)CD172a(−/low)) and cDC2 (MHCII(high)CADM1(high)CD172a(+)) phenotypes were confirmed by the expression of characteristic cDC1 and cDC2 transcripts (FLT3, XCR1 and FCER1α). Among all lymphoid tissues, the spleen had the highest frequency of total cDCs. The cDC1:cDC2 ratio showed that all lymph tissues had higher levels of cDC1 than levels of cDC2. DEC205(+) cDCs were found in all analyzed tissues, albeit with different frequencies. Our research will facilitate the study on the function of these cells and the investigation of the strategies for DEC205 targeting and functional studies.
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spelling pubmed-71126462020-04-02 Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes Parra-Sánchez, Héctor Puebla-Clark, Lucinda Reséndiz, Mónica Valenzuela, Olivia Hernández, Jesús Mol Immunol Article Conventional dendritic cells (cDCs) are divided into the following different subtypes: cDC1, which promotes a Th1 response, and cDC2, which stimulates a Th2 and Th17 response. These cells have not been characterized in porcine lymphoid tissues. DEC205 is a receptor that increases antigen presentation and allows DCs to cross-present antigens. The objectives of this work were to characterize cDCs subsets in the tonsil, submaxillary and mesenteric lymph nodes and spleen lymphoid tissues and to determine their expression of DEC205 by flow cytometry. The cDC1 (MHCII(high)CADM1(high)CD172a(−/low)) and cDC2 (MHCII(high)CADM1(high)CD172a(+)) phenotypes were confirmed by the expression of characteristic cDC1 and cDC2 transcripts (FLT3, XCR1 and FCER1α). Among all lymphoid tissues, the spleen had the highest frequency of total cDCs. The cDC1:cDC2 ratio showed that all lymph tissues had higher levels of cDC1 than levels of cDC2. DEC205(+) cDCs were found in all analyzed tissues, albeit with different frequencies. Our research will facilitate the study on the function of these cells and the investigation of the strategies for DEC205 targeting and functional studies. Elsevier Ltd. 2018-04 2018-02-10 /pmc/articles/PMC7112646/ /pubmed/29433077 http://dx.doi.org/10.1016/j.molimm.2018.02.003 Text en © 2018 Elsevier Ltd. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Parra-Sánchez, Héctor
Puebla-Clark, Lucinda
Reséndiz, Mónica
Valenzuela, Olivia
Hernández, Jesús
Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes
title Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes
title_full Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes
title_fullStr Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes
title_full_unstemmed Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes
title_short Characterization and expression of DEC205 in the cDC1 and cDC2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes
title_sort characterization and expression of dec205 in the cdc1 and cdc2 subsets of porcine dendritic cells from spleen, tonsil, and submaxillary and mesenteric lymph nodes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7112646/
https://www.ncbi.nlm.nih.gov/pubmed/29433077
http://dx.doi.org/10.1016/j.molimm.2018.02.003
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