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Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway

BACKGROUND: Preconditioning with inflammatory stimuli is used to improve the secretion of anti-inflammatory agents in stem cells from variant species such as mouse, human, and dog. However, there are only few studies on feline stem cells. OBJECTIVES: This study aimed to evaluate the immune regulator...

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Autores principales: Park, Seol-Gi, An, Ju-Hyun, Li, Qiang, Chae, Hyung-Kyu, Park, Su-Min, Lee, Jeong-Hwa, Ahn, Jin-Ok, Song, Woo-Jin, Youn, Hwa-Young
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Society of Veterinary Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007449/
https://www.ncbi.nlm.nih.gov/pubmed/33774932
http://dx.doi.org/10.4142/jvs.2021.22.e16
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author Park, Seol-Gi
An, Ju-Hyun
Li, Qiang
Chae, Hyung-Kyu
Park, Su-Min
Lee, Jeong-Hwa
Ahn, Jin-Ok
Song, Woo-Jin
Youn, Hwa-Young
author_facet Park, Seol-Gi
An, Ju-Hyun
Li, Qiang
Chae, Hyung-Kyu
Park, Su-Min
Lee, Jeong-Hwa
Ahn, Jin-Ok
Song, Woo-Jin
Youn, Hwa-Young
author_sort Park, Seol-Gi
collection PubMed
description BACKGROUND: Preconditioning with inflammatory stimuli is used to improve the secretion of anti-inflammatory agents in stem cells from variant species such as mouse, human, and dog. However, there are only few studies on feline stem cells. OBJECTIVES: This study aimed to evaluate the immune regulatory capacity of feline adipose tissue-derived (fAT) mesenchymal stem cells (MSCs) pretreated with interferon-gamma (IFN-γ). METHODS: To assess the interaction of lymphocytes and macrophages with IFN-γ-pretreated fAT-MSCs, mouse splenocytes and RAW 264.7 cells were cultured with the conditioned media from IFN-γ-pretreated MSCs. RESULTS: Pretreatment with IFN-γ increased the gene expression levels of cyclooxygenase-2, indoleamine 2,3-dioxygenase, hepatocyte growth factor, and transforming growth factor-beta 1 in the MSCs. The conditioned media from IFN-γ-pretreated MSCs increased the expression levels of M2 macrophage markers and regulatory T-cell markers compared to those in the conditioned media from naive MSCs. Further, prostaglandin E(2) (PGE(2)) inhibitor NS-398 attenuated the immunoregulatory potential of MSCs, suggesting that the increased PGE(2) levels induced by IFN-γ stimulation is a crucial factor in the immune regulatory capacity of MSCs pretreated with IFN-γ. CONCLUSIONS: IFN-γ pretreatment improves the immune regulatory profile of fAT-MSCs mainly via the secretion of PGE(2), which induces macrophage polarization and increases regulatory T-cell numbers.
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spelling pubmed-80074492021-04-07 Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway Park, Seol-Gi An, Ju-Hyun Li, Qiang Chae, Hyung-Kyu Park, Su-Min Lee, Jeong-Hwa Ahn, Jin-Ok Song, Woo-Jin Youn, Hwa-Young J Vet Sci Original Article BACKGROUND: Preconditioning with inflammatory stimuli is used to improve the secretion of anti-inflammatory agents in stem cells from variant species such as mouse, human, and dog. However, there are only few studies on feline stem cells. OBJECTIVES: This study aimed to evaluate the immune regulatory capacity of feline adipose tissue-derived (fAT) mesenchymal stem cells (MSCs) pretreated with interferon-gamma (IFN-γ). METHODS: To assess the interaction of lymphocytes and macrophages with IFN-γ-pretreated fAT-MSCs, mouse splenocytes and RAW 264.7 cells were cultured with the conditioned media from IFN-γ-pretreated MSCs. RESULTS: Pretreatment with IFN-γ increased the gene expression levels of cyclooxygenase-2, indoleamine 2,3-dioxygenase, hepatocyte growth factor, and transforming growth factor-beta 1 in the MSCs. The conditioned media from IFN-γ-pretreated MSCs increased the expression levels of M2 macrophage markers and regulatory T-cell markers compared to those in the conditioned media from naive MSCs. Further, prostaglandin E(2) (PGE(2)) inhibitor NS-398 attenuated the immunoregulatory potential of MSCs, suggesting that the increased PGE(2) levels induced by IFN-γ stimulation is a crucial factor in the immune regulatory capacity of MSCs pretreated with IFN-γ. CONCLUSIONS: IFN-γ pretreatment improves the immune regulatory profile of fAT-MSCs mainly via the secretion of PGE(2), which induces macrophage polarization and increases regulatory T-cell numbers. The Korean Society of Veterinary Science 2021-03 2021-02-10 /pmc/articles/PMC8007449/ /pubmed/33774932 http://dx.doi.org/10.4142/jvs.2021.22.e16 Text en © 2021 The Korean Society of Veterinary Science https://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (https://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Park, Seol-Gi
An, Ju-Hyun
Li, Qiang
Chae, Hyung-Kyu
Park, Su-Min
Lee, Jeong-Hwa
Ahn, Jin-Ok
Song, Woo-Jin
Youn, Hwa-Young
Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway
title Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway
title_full Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway
title_fullStr Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway
title_full_unstemmed Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway
title_short Feline adipose tissue-derived mesenchymal stem cells pretreated with IFN-γ enhance immunomodulatory effects through the PGE(2) pathway
title_sort feline adipose tissue-derived mesenchymal stem cells pretreated with ifn-γ enhance immunomodulatory effects through the pge(2) pathway
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007449/
https://www.ncbi.nlm.nih.gov/pubmed/33774932
http://dx.doi.org/10.4142/jvs.2021.22.e16
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