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Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study

BACKGROUND: The use of mesenchymal stem cells (MSCs) is being extensively studied in clinical trials in the setting of various diseases including diabetes, stroke, and progressive multiple sclerosis. The unique immunomodulatory properties of MSCs also point them as a possible therapeutic tool during...

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Autores principales: Laroye, Caroline, Boufenzer, Amir, Jolly, Lucie, Cunat, Lisiane, Alauzet, Corentine, Merlin, Jean-Louis, Yguel, Clémence, Bensoussan, Danièle, Reppel, Loïc, Gibot, Sébastien
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598309/
https://www.ncbi.nlm.nih.gov/pubmed/31248453
http://dx.doi.org/10.1186/s13287-019-1295-9
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author Laroye, Caroline
Boufenzer, Amir
Jolly, Lucie
Cunat, Lisiane
Alauzet, Corentine
Merlin, Jean-Louis
Yguel, Clémence
Bensoussan, Danièle
Reppel, Loïc
Gibot, Sébastien
author_facet Laroye, Caroline
Boufenzer, Amir
Jolly, Lucie
Cunat, Lisiane
Alauzet, Corentine
Merlin, Jean-Louis
Yguel, Clémence
Bensoussan, Danièle
Reppel, Loïc
Gibot, Sébastien
author_sort Laroye, Caroline
collection PubMed
description BACKGROUND: The use of mesenchymal stem cells (MSCs) is being extensively studied in clinical trials in the setting of various diseases including diabetes, stroke, and progressive multiple sclerosis. The unique immunomodulatory properties of MSCs also point them as a possible therapeutic tool during sepsis and septic shock, a devastating syndrome associated with 30–35% mortality. However, MSCs are not equal regarding their activity, depending on their tissue origin. Here, we aimed at comparing the in vivo properties of MSCs according to their tissue source (bone marrow (BM) versus Wharton’s jelly (WJ)) in a murine cecal ligation and puncture (CLP) model of sepsis that mimics a human peritonitis. We hypothesized that MSC properties may vary depending on their tissue source in the setting of sepsis. METHODS: CLP, adult, male, C57BL/6 mice were randomized in 3 groups receiving respectively 0.25 × 10(6) BM-MSCs, 0.25 × 10(6) WJ-MSCs, or 150 μL phosphate-buffered saline (PBS) intravenously 24 h after the CLP procedure. RESULTS: We observed that both types of MSCs regulated leukocyte trafficking and reduced organ dysfunction, while only WJ-MSCs were able to improve bacterial clearance and survival. CONCLUSION: This study highlights the importance to determine the most appropriate source of MSCs for a given therapeutic indication and suggests a better profile for WJ-MSCs during sepsis.
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spelling pubmed-65983092019-07-11 Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study Laroye, Caroline Boufenzer, Amir Jolly, Lucie Cunat, Lisiane Alauzet, Corentine Merlin, Jean-Louis Yguel, Clémence Bensoussan, Danièle Reppel, Loïc Gibot, Sébastien Stem Cell Res Ther Research BACKGROUND: The use of mesenchymal stem cells (MSCs) is being extensively studied in clinical trials in the setting of various diseases including diabetes, stroke, and progressive multiple sclerosis. The unique immunomodulatory properties of MSCs also point them as a possible therapeutic tool during sepsis and septic shock, a devastating syndrome associated with 30–35% mortality. However, MSCs are not equal regarding their activity, depending on their tissue origin. Here, we aimed at comparing the in vivo properties of MSCs according to their tissue source (bone marrow (BM) versus Wharton’s jelly (WJ)) in a murine cecal ligation and puncture (CLP) model of sepsis that mimics a human peritonitis. We hypothesized that MSC properties may vary depending on their tissue source in the setting of sepsis. METHODS: CLP, adult, male, C57BL/6 mice were randomized in 3 groups receiving respectively 0.25 × 10(6) BM-MSCs, 0.25 × 10(6) WJ-MSCs, or 150 μL phosphate-buffered saline (PBS) intravenously 24 h after the CLP procedure. RESULTS: We observed that both types of MSCs regulated leukocyte trafficking and reduced organ dysfunction, while only WJ-MSCs were able to improve bacterial clearance and survival. CONCLUSION: This study highlights the importance to determine the most appropriate source of MSCs for a given therapeutic indication and suggests a better profile for WJ-MSCs during sepsis. BioMed Central 2019-06-27 /pmc/articles/PMC6598309/ /pubmed/31248453 http://dx.doi.org/10.1186/s13287-019-1295-9 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Laroye, Caroline
Boufenzer, Amir
Jolly, Lucie
Cunat, Lisiane
Alauzet, Corentine
Merlin, Jean-Louis
Yguel, Clémence
Bensoussan, Danièle
Reppel, Loïc
Gibot, Sébastien
Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study
title Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study
title_full Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study
title_fullStr Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study
title_full_unstemmed Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study
title_short Bone marrow vs Wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study
title_sort bone marrow vs wharton’s jelly mesenchymal stem cells in experimental sepsis: a comparative study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6598309/
https://www.ncbi.nlm.nih.gov/pubmed/31248453
http://dx.doi.org/10.1186/s13287-019-1295-9
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