Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.

In vitro generation of dendritic cells (DCs) is advantageous for overcoming the low frequency of primary DCs and the difficulty of applying isolation techniques for studying DC immunobiology. The culture of bone marrow cells with granulocyte-macrophage colony-stimulating factor (GM-CSF) has been use...

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Main Authors: Sang Eun Kim, Jeong Ho Hwang, Young Kyu Kim, Hoon Taek Lee
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0223590
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spelling doaj-3871fbd59a654721adee6006658f9b542021-03-03T21:15:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-011411e022359010.1371/journal.pone.0223590Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.Sang Eun KimJeong Ho HwangYoung Kyu KimHoon Taek LeeIn vitro generation of dendritic cells (DCs) is advantageous for overcoming the low frequency of primary DCs and the difficulty of applying isolation techniques for studying DC immunobiology. The culture of bone marrow cells with granulocyte-macrophage colony-stimulating factor (GM-CSF) has been used extensively to generate bone marrow-derived dendritic cells (BMDCs). Studies have reported the heterogeneity of cells grown in murine GM-CSF culture based on the levels of MHCII expression. Although porcine DCs are generated by this classical method, the exact characteristics of the BMDC population have not yet been defined. In this study, we discriminated GM-CSF-grown BMDCs from gnotobiotic miniature pigs according to several criteria including morphology, phenotype, gene expression pattern and function. We showed that porcine BMDCs were heterogeneous cells that differentially expressed MHCII. MHCIIhigh cells displayed more representative of DC-like morphology and phenotype, including costimulatory molecules, as well as they showed a superior T cell priming capacity as compared to MHCIIlow cell. Our data showed that the difference in MHCIIhigh and MHCIIlow cell populations involved distinct maturation states rather than the presence of different cell types. Overall, characterization of porcine BMDC cultures provides important information about this widely used cellular model.https://doi.org/10.1371/journal.pone.0223590
collection DOAJ
language English
format Article
sources DOAJ
author Sang Eun Kim
Jeong Ho Hwang
Young Kyu Kim
Hoon Taek Lee
spellingShingle Sang Eun Kim
Jeong Ho Hwang
Young Kyu Kim
Hoon Taek Lee
Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.
PLoS ONE
author_facet Sang Eun Kim
Jeong Ho Hwang
Young Kyu Kim
Hoon Taek Lee
author_sort Sang Eun Kim
title Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.
title_short Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.
title_full Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.
title_fullStr Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.
title_full_unstemmed Heterogeneity of porcine bone marrow-derived dendritic cells induced by GM-CSF.
title_sort heterogeneity of porcine bone marrow-derived dendritic cells induced by gm-csf.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description In vitro generation of dendritic cells (DCs) is advantageous for overcoming the low frequency of primary DCs and the difficulty of applying isolation techniques for studying DC immunobiology. The culture of bone marrow cells with granulocyte-macrophage colony-stimulating factor (GM-CSF) has been used extensively to generate bone marrow-derived dendritic cells (BMDCs). Studies have reported the heterogeneity of cells grown in murine GM-CSF culture based on the levels of MHCII expression. Although porcine DCs are generated by this classical method, the exact characteristics of the BMDC population have not yet been defined. In this study, we discriminated GM-CSF-grown BMDCs from gnotobiotic miniature pigs according to several criteria including morphology, phenotype, gene expression pattern and function. We showed that porcine BMDCs were heterogeneous cells that differentially expressed MHCII. MHCIIhigh cells displayed more representative of DC-like morphology and phenotype, including costimulatory molecules, as well as they showed a superior T cell priming capacity as compared to MHCIIlow cell. Our data showed that the difference in MHCIIhigh and MHCIIlow cell populations involved distinct maturation states rather than the presence of different cell types. Overall, characterization of porcine BMDC cultures provides important information about this widely used cellular model.
url https://doi.org/10.1371/journal.pone.0223590
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