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Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis

Tertiary lymphoid structures (TLS) develop in the kidneys of lupus-prone mice and systemic lupus erythematosus (SLE) patients with lupus nephritis (LN). Here we investigated the presence of mesenchymal stem cells (MSCs) in the development of TLS in murine LN, as well as the role of human MSCs as lym...

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Autores principales: Dorraji, S. Esmaeil, Hovd, Aud-Malin K., Kanapathippillai, Premasany, Bakland, Gunnstein, Eilertsen, Gro Østli, Figenschau, Stine L., Fenton, Kristin A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959845/
https://www.ncbi.nlm.nih.gov/pubmed/29777158
http://dx.doi.org/10.1038/s41598-018-26265-z
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author Dorraji, S. Esmaeil
Hovd, Aud-Malin K.
Kanapathippillai, Premasany
Bakland, Gunnstein
Eilertsen, Gro Østli
Figenschau, Stine L.
Fenton, Kristin A.
author_facet Dorraji, S. Esmaeil
Hovd, Aud-Malin K.
Kanapathippillai, Premasany
Bakland, Gunnstein
Eilertsen, Gro Østli
Figenschau, Stine L.
Fenton, Kristin A.
author_sort Dorraji, S. Esmaeil
collection PubMed
description Tertiary lymphoid structures (TLS) develop in the kidneys of lupus-prone mice and systemic lupus erythematosus (SLE) patients with lupus nephritis (LN). Here we investigated the presence of mesenchymal stem cells (MSCs) in the development of TLS in murine LN, as well as the role of human MSCs as lymphoid tissue organizer (LTo) cells on the activation of CD4+ T cells from three groups of donors including Healthy, SLE and LN patients. Mesenchymal stem like cells were detected within the pelvic wall and TLS in kidneys of lupus-prone mice. An increase in LTβ, CXCL13, CCL19, VCAM1 and ICAM1 gene expressions were detected during the development of murine LN. Human MSCs stimulated with the pro-inflammatory cytokines TNF-α and IL-1β significantly increased the expression of CCL19, VCAM1, ICAM1, TNF-α, and IL-1β. Stimulated MSCs induced proliferation of CD4(+) T cells, but an inhibitory effect was observed when in co-culture with non-stimulated MSCs. A contact dependent increase in Th2 and Th17 subsets were observed for T cells from the Healthy group after co-culture with stimulated MSCs. Our data suggest that tissue-specific or/and migratory MSCs could have pivotal roles as LTo cells in accelerating early inflammatory processes and initiating the formation of kidney specific TLS in chronic inflammatory conditions.
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spelling pubmed-59598452018-05-24 Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis Dorraji, S. Esmaeil Hovd, Aud-Malin K. Kanapathippillai, Premasany Bakland, Gunnstein Eilertsen, Gro Østli Figenschau, Stine L. Fenton, Kristin A. Sci Rep Article Tertiary lymphoid structures (TLS) develop in the kidneys of lupus-prone mice and systemic lupus erythematosus (SLE) patients with lupus nephritis (LN). Here we investigated the presence of mesenchymal stem cells (MSCs) in the development of TLS in murine LN, as well as the role of human MSCs as lymphoid tissue organizer (LTo) cells on the activation of CD4+ T cells from three groups of donors including Healthy, SLE and LN patients. Mesenchymal stem like cells were detected within the pelvic wall and TLS in kidneys of lupus-prone mice. An increase in LTβ, CXCL13, CCL19, VCAM1 and ICAM1 gene expressions were detected during the development of murine LN. Human MSCs stimulated with the pro-inflammatory cytokines TNF-α and IL-1β significantly increased the expression of CCL19, VCAM1, ICAM1, TNF-α, and IL-1β. Stimulated MSCs induced proliferation of CD4(+) T cells, but an inhibitory effect was observed when in co-culture with non-stimulated MSCs. A contact dependent increase in Th2 and Th17 subsets were observed for T cells from the Healthy group after co-culture with stimulated MSCs. Our data suggest that tissue-specific or/and migratory MSCs could have pivotal roles as LTo cells in accelerating early inflammatory processes and initiating the formation of kidney specific TLS in chronic inflammatory conditions. Nature Publishing Group UK 2018-05-18 /pmc/articles/PMC5959845/ /pubmed/29777158 http://dx.doi.org/10.1038/s41598-018-26265-z Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Dorraji, S. Esmaeil
Hovd, Aud-Malin K.
Kanapathippillai, Premasany
Bakland, Gunnstein
Eilertsen, Gro Østli
Figenschau, Stine L.
Fenton, Kristin A.
Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis
title Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis
title_full Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis
title_fullStr Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis
title_full_unstemmed Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis
title_short Mesenchymal stem cells and T cells in the formation of Tertiary Lymphoid Structures in Lupus Nephritis
title_sort mesenchymal stem cells and t cells in the formation of tertiary lymphoid structures in lupus nephritis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5959845/
https://www.ncbi.nlm.nih.gov/pubmed/29777158
http://dx.doi.org/10.1038/s41598-018-26265-z
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