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The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model

Inflammasomes are cytosolic, multiprotein complexes that act at the frontline of the immune responses by recognizing pathogen- or danger-associated molecular patterns or abnormal host molecules. Mesenchymal stem cells (MSCs) have been reported to possess multipotency to differentiate into various ce...

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Autores principales: Ahn, Ji-Su, Seo, Yoojin, Oh, Su-Jeong, Yang, Ji Won, Shin, Ye Young, Lee, Byung-Chul, Kang, Kyung-Sun, Sung, Eui-Suk, Lee, Byung-Joo, Mohammadpour, Hemn, Hur, Jin, Shin, Tae-Hoon, Kim, Hyung-Sik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society for Biochemistry and Molecular Biology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330809/
https://www.ncbi.nlm.nih.gov/pubmed/32475381
http://dx.doi.org/10.5483/BMBRep.2020.53.6.065
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author Ahn, Ji-Su
Seo, Yoojin
Oh, Su-Jeong
Yang, Ji Won
Shin, Ye Young
Lee, Byung-Chul
Kang, Kyung-Sun
Sung, Eui-Suk
Lee, Byung-Joo
Mohammadpour, Hemn
Hur, Jin
Shin, Tae-Hoon
Kim, Hyung-Sik
author_facet Ahn, Ji-Su
Seo, Yoojin
Oh, Su-Jeong
Yang, Ji Won
Shin, Ye Young
Lee, Byung-Chul
Kang, Kyung-Sun
Sung, Eui-Suk
Lee, Byung-Joo
Mohammadpour, Hemn
Hur, Jin
Shin, Tae-Hoon
Kim, Hyung-Sik
author_sort Ahn, Ji-Su
collection PubMed
description Inflammasomes are cytosolic, multiprotein complexes that act at the frontline of the immune responses by recognizing pathogen- or danger-associated molecular patterns or abnormal host molecules. Mesenchymal stem cells (MSCs) have been reported to possess multipotency to differentiate into various cell types and immunoregulatory effects. In this study, we investigated the expression and functional regulation of NLR Family Pyrin Domain Containing 3 (NLRP3) inflammasome in human umbilical cord blood-derived MSCs (hUCB-MSCs). hUCB-MSCs expressed inflammasome components that are necessary for its complex assembly. Interestingly, NLRP3 inflammasome activation suppressed the differentiation of hUCB-MSCs into osteoblasts, which was restored when the expression of adaptor proteins for inflammasome assembly was inhibited. Moreover, the suppressive effects of MSCs on T cell responses and the macrophage activation were augmented in response to NLRP3 activation. In vivo studies using colitic mice revealed that the protective abilities of hUCB-MSCs increased after NLRP3 stimulation. In conclusion, our findings suggest that the NLRP3 inflammasome components are expressed in hUCB-MSCs and its activation can regulate the differentiation capability and the immunomodulatory effects of hUCB-MSCs.
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spelling pubmed-73308092020-07-14 The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model Ahn, Ji-Su Seo, Yoojin Oh, Su-Jeong Yang, Ji Won Shin, Ye Young Lee, Byung-Chul Kang, Kyung-Sun Sung, Eui-Suk Lee, Byung-Joo Mohammadpour, Hemn Hur, Jin Shin, Tae-Hoon Kim, Hyung-Sik BMB Rep Article Inflammasomes are cytosolic, multiprotein complexes that act at the frontline of the immune responses by recognizing pathogen- or danger-associated molecular patterns or abnormal host molecules. Mesenchymal stem cells (MSCs) have been reported to possess multipotency to differentiate into various cell types and immunoregulatory effects. In this study, we investigated the expression and functional regulation of NLR Family Pyrin Domain Containing 3 (NLRP3) inflammasome in human umbilical cord blood-derived MSCs (hUCB-MSCs). hUCB-MSCs expressed inflammasome components that are necessary for its complex assembly. Interestingly, NLRP3 inflammasome activation suppressed the differentiation of hUCB-MSCs into osteoblasts, which was restored when the expression of adaptor proteins for inflammasome assembly was inhibited. Moreover, the suppressive effects of MSCs on T cell responses and the macrophage activation were augmented in response to NLRP3 activation. In vivo studies using colitic mice revealed that the protective abilities of hUCB-MSCs increased after NLRP3 stimulation. In conclusion, our findings suggest that the NLRP3 inflammasome components are expressed in hUCB-MSCs and its activation can regulate the differentiation capability and the immunomodulatory effects of hUCB-MSCs. Korean Society for Biochemistry and Molecular Biology 2020-06-30 2020-06-30 /pmc/articles/PMC7330809/ /pubmed/32475381 http://dx.doi.org/10.5483/BMBRep.2020.53.6.065 Text en Copyright © 2020 by the The Korean Society for Biochemistry and Molecular Biology This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://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 Article
Ahn, Ji-Su
Seo, Yoojin
Oh, Su-Jeong
Yang, Ji Won
Shin, Ye Young
Lee, Byung-Chul
Kang, Kyung-Sun
Sung, Eui-Suk
Lee, Byung-Joo
Mohammadpour, Hemn
Hur, Jin
Shin, Tae-Hoon
Kim, Hyung-Sik
The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model
title The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model
title_full The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model
title_fullStr The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model
title_full_unstemmed The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model
title_short The activation of NLRP3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model
title_sort activation of nlrp3 inflammasome potentiates the immunomodulatory abilities of mesenchymal stem cells in a murine colitis model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7330809/
https://www.ncbi.nlm.nih.gov/pubmed/32475381
http://dx.doi.org/10.5483/BMBRep.2020.53.6.065
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