De novo interleukin-10 production primed by Lactobacillus sakei CVL-001 amplifies the immunomodulatory abilities of mesenchymal stem cells to alleviate colitis

Mesenchymal stem cells (MSCs) hold therapeutic promise for treating inflammatory bowel disease (IBD) owing to their immunomodulatory properties. Currently, pre-conditioning strategies with several beneficial agents have been applied to enhance the efficacy of MSCs in treating IBDs. Probiotics are in...

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Veröffentlicht in:Biomedicine & pharmacotherapy 2025-01, Vol.182, p.117745, Article 117745
Hauptverfasser: Nguyen, Phuong Thao, Seo, Yoojin, Ahn, Ji-Su, Oh, Su-Jeong, Park, Hee-Jeong, Yu, Jeong Hyun, Kim, Seong Hui, Lee, Yunji, Yang, Ji Won, Cho, Jaejin, Kang, Min-Jung, Park, Jong-Hwan, Kim, Hyung-Sik
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container_start_page 117745
container_title Biomedicine & pharmacotherapy
container_volume 182
creator Nguyen, Phuong Thao
Seo, Yoojin
Ahn, Ji-Su
Oh, Su-Jeong
Park, Hee-Jeong
Yu, Jeong Hyun
Kim, Seong Hui
Lee, Yunji
Yang, Ji Won
Cho, Jaejin
Kang, Min-Jung
Park, Jong-Hwan
Kim, Hyung-Sik
description Mesenchymal stem cells (MSCs) hold therapeutic promise for treating inflammatory bowel disease (IBD) owing to their immunomodulatory properties. Currently, pre-conditioning strategies with several beneficial agents have been applied to enhance the efficacy of MSCs in treating IBDs. Probiotics are increasingly acknowledged as supplemental therapy for IBD; however, their potential benefits in MSCs-based therapy remain largely unexplored. In this study, we hypothesized that pretreating MSCs with Lactobacillus sakei CVL-001 (L. sakei CVL-001), a representative probiotic strain, could improve their therapeutic effectiveness for IBD. In line with this hypothesis, we noted that pretreatment with L. sakei CVL-001 significantly induced IL-10 secretion in MSCs via the activation of the STAT3 signaling pathway. These primed MSCs reduced pro-inflammatory cytokine production in LPS/IFN-γ-treated macrophages and promoted an M2 phenotype, associated with immunoregulation and tissue repair, in undifferentiated macrophages. In addition, their conditioned media significantly reduced the proliferation capacity of Jurkat T cells and splenocytes, while the neutralization of IL-10 reversed these phenomena. Furthermore, MSCs treated with L. sakei CVL-001 mitigated inflammatory responses and promoted epithelial regeneration, leading to accelerated recovery from disease symptoms and improved survival rates compared to naive MSCs in a DSS-induced colitis mouse model. In conclusion, our findings suggest that probiotics, such as L. sakei CVL-001, can improve the therapeutic efficacy of MSCs for treating IBD. [Display omitted] •L. sakei CVL-001 primes human MSCs to produce IL-10, through the activation of the STAT3 signaling pathway.•IL-10 from L. sakei CVL-001-primed MSCs suppresses M1 macrophage activation, while promoting M2 macrophage polarization.•L. sakei CVL-001-primed MSCs reduce the proliferation of both ConA-activated T cells and splenocytes.•Treatment with L. sakei CVL-001-primed MSCs in murine colitis model alleviates inflammation and enhances regeneration.
doi_str_mv 10.1016/j.biopha.2024.117745
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Currently, pre-conditioning strategies with several beneficial agents have been applied to enhance the efficacy of MSCs in treating IBDs. Probiotics are increasingly acknowledged as supplemental therapy for IBD; however, their potential benefits in MSCs-based therapy remain largely unexplored. In this study, we hypothesized that pretreating MSCs with Lactobacillus sakei CVL-001 (L. sakei CVL-001), a representative probiotic strain, could improve their therapeutic effectiveness for IBD. In line with this hypothesis, we noted that pretreatment with L. sakei CVL-001 significantly induced IL-10 secretion in MSCs via the activation of the STAT3 signaling pathway. These primed MSCs reduced pro-inflammatory cytokine production in LPS/IFN-γ-treated macrophages and promoted an M2 phenotype, associated with immunoregulation and tissue repair, in undifferentiated macrophages. 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[Display omitted] •L. sakei CVL-001 primes human MSCs to produce IL-10, through the activation of the STAT3 signaling pathway.•IL-10 from L. sakei CVL-001-primed MSCs suppresses M1 macrophage activation, while promoting M2 macrophage polarization.•L. sakei CVL-001-primed MSCs reduce the proliferation of both ConA-activated T cells and splenocytes.•Treatment with L. sakei CVL-001-primed MSCs in murine colitis model alleviates inflammation and enhances regeneration.</description><identifier>ISSN: 0753-3322</identifier><identifier>ISSN: 1950-6007</identifier><identifier>EISSN: 1950-6007</identifier><identifier>DOI: 10.1016/j.biopha.2024.117745</identifier><identifier>PMID: 39705909</identifier><language>eng</language><publisher>France: Elsevier Masson SAS</publisher><subject>Animals ; Cell Proliferation - drug effects ; Colitis - chemically induced ; Colitis - immunology ; Colitis - microbiology ; Colitis - therapy ; Dextran Sulfate ; Disease Models, Animal ; Humans ; Immunomodulation ; Inflammatory Bowel Disease ; Interleukin-10 - metabolism ; Lactobacillus sakei CVL-001 ; Latilactobacillus sakei ; Macrophages - drug effects ; Macrophages - immunology ; Macrophages - metabolism ; Male ; Mesenchymal Stem Cell Transplantation - methods ; Mesenchymal Stem Cells ; Mesenchymal Stem Cells - immunology ; Mesenchymal Stem Cells - metabolism ; Mice ; Mice, Inbred C57BL ; Probiotics - pharmacology ; Regeneration</subject><ispartof>Biomedicine &amp; pharmacotherapy, 2025-01, Vol.182, p.117745, Article 117745</ispartof><rights>2024 The Authors</rights><rights>Copyright © 2024 The Authors. 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In addition, their conditioned media significantly reduced the proliferation capacity of Jurkat T cells and splenocytes, while the neutralization of IL-10 reversed these phenomena. Furthermore, MSCs treated with L. sakei CVL-001 mitigated inflammatory responses and promoted epithelial regeneration, leading to accelerated recovery from disease symptoms and improved survival rates compared to naive MSCs in a DSS-induced colitis mouse model. In conclusion, our findings suggest that probiotics, such as L. sakei CVL-001, can improve the therapeutic efficacy of MSCs for treating IBD. [Display omitted] •L. sakei CVL-001 primes human MSCs to produce IL-10, through the activation of the STAT3 signaling pathway.•IL-10 from L. sakei CVL-001-primed MSCs suppresses M1 macrophage activation, while promoting M2 macrophage polarization.•L. sakei CVL-001-primed MSCs reduce the proliferation of both ConA-activated T cells and splenocytes.•Treatment with L. sakei CVL-001-primed MSCs in murine colitis model alleviates inflammation and enhances regeneration.</abstract><cop>France</cop><pub>Elsevier Masson SAS</pub><pmid>39705909</pmid><doi>10.1016/j.biopha.2024.117745</doi><oa>free_for_read</oa></addata></record>
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subjects Animals
Cell Proliferation - drug effects
Colitis - chemically induced
Colitis - immunology
Colitis - microbiology
Colitis - therapy
Dextran Sulfate
Disease Models, Animal
Humans
Immunomodulation
Inflammatory Bowel Disease
Interleukin-10 - metabolism
Lactobacillus sakei CVL-001
Latilactobacillus sakei
Macrophages - drug effects
Macrophages - immunology
Macrophages - metabolism
Male
Mesenchymal Stem Cell Transplantation - methods
Mesenchymal Stem Cells
Mesenchymal Stem Cells - immunology
Mesenchymal Stem Cells - metabolism
Mice
Mice, Inbred C57BL
Probiotics - pharmacology
Regeneration
title De novo interleukin-10 production primed by Lactobacillus sakei CVL-001 amplifies the immunomodulatory abilities of mesenchymal stem cells to alleviate colitis
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