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Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis

Dendritic cells have been known as a member of strong innate immune cells against infectious organelles. In this study, we evaluated the cytokine expression of splenic dendritic cells in chronic mouse toxoplasmosis by tissue cyst-forming Me49 strain and demonstrated the distribution of lymphoid dend...

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Autores principales: Nam, Ho-Woo, Ahn, Hye-Jin, Yang, Hyun-Jong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society for Parasitology 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121066/
https://www.ncbi.nlm.nih.gov/pubmed/21738265
http://dx.doi.org/10.3347/kjp.2011.49.2.109
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author Nam, Ho-Woo
Ahn, Hye-Jin
Yang, Hyun-Jong
author_facet Nam, Ho-Woo
Ahn, Hye-Jin
Yang, Hyun-Jong
author_sort Nam, Ho-Woo
collection PubMed
description Dendritic cells have been known as a member of strong innate immune cells against infectious organelles. In this study, we evaluated the cytokine expression of splenic dendritic cells in chronic mouse toxoplasmosis by tissue cyst-forming Me49 strain and demonstrated the distribution of lymphoid dendritic cells by fluorescence-activated cell sorter (FACS). Pro-inflammatory cytokines, such as IL-1α, IL-1β, IL-6, and IL-10 increased rapidly at week 1 post-infection (PI) and peaked at week 3 PI. Serum IL-10 level followed the similar patterns. FACS analysis showed that the number of CD8α(+)/CD11c(+) splenic dendritic cells increased at week 1 and peaked at week 3 PI. In conclusion, mouse splenic dendritic cells showed early and rapid cytokine changes and may have important protective roles in early phases of murine toxoplasmosis.
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spelling pubmed-31210662011-07-07 Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis Nam, Ho-Woo Ahn, Hye-Jin Yang, Hyun-Jong Korean J Parasitol Original Article Dendritic cells have been known as a member of strong innate immune cells against infectious organelles. In this study, we evaluated the cytokine expression of splenic dendritic cells in chronic mouse toxoplasmosis by tissue cyst-forming Me49 strain and demonstrated the distribution of lymphoid dendritic cells by fluorescence-activated cell sorter (FACS). Pro-inflammatory cytokines, such as IL-1α, IL-1β, IL-6, and IL-10 increased rapidly at week 1 post-infection (PI) and peaked at week 3 PI. Serum IL-10 level followed the similar patterns. FACS analysis showed that the number of CD8α(+)/CD11c(+) splenic dendritic cells increased at week 1 and peaked at week 3 PI. In conclusion, mouse splenic dendritic cells showed early and rapid cytokine changes and may have important protective roles in early phases of murine toxoplasmosis. The Korean Society for Parasitology 2011-06 2011-06-14 /pmc/articles/PMC3121066/ /pubmed/21738265 http://dx.doi.org/10.3347/kjp.2011.49.2.109 Text en © 2011, Korean Society for Parasitology http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Nam, Ho-Woo
Ahn, Hye-Jin
Yang, Hyun-Jong
Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis
title Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis
title_full Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis
title_fullStr Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis
title_full_unstemmed Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis
title_short Pro-inflammatory Cytokine Expression of Spleen Dendritic Cells in Mouse Toxoplasmosis
title_sort pro-inflammatory cytokine expression of spleen dendritic cells in mouse toxoplasmosis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3121066/
https://www.ncbi.nlm.nih.gov/pubmed/21738265
http://dx.doi.org/10.3347/kjp.2011.49.2.109
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