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Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation

Bone marrow mesenchymal stromal cells (MSCs) play a crucial role in the regulation of hematopoiesis. These cells affect the process through direct cell–cell contact, as well as releasing various trophic factors and extracellular vehicles (EVs) into the bone marrow microenvironment. MSC-derived EVs (...

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Autores principales: Sarvar, Davod Pashoutan, Effatpanah, Hosein, Akbarzadehlaleh, Parvin, Shamsasenjan, Karim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109321/
https://www.ncbi.nlm.nih.gov/pubmed/35578300
http://dx.doi.org/10.1186/s13287-022-02875-3
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author Sarvar, Davod Pashoutan
Effatpanah, Hosein
Akbarzadehlaleh, Parvin
Shamsasenjan, Karim
author_facet Sarvar, Davod Pashoutan
Effatpanah, Hosein
Akbarzadehlaleh, Parvin
Shamsasenjan, Karim
author_sort Sarvar, Davod Pashoutan
collection PubMed
description Bone marrow mesenchymal stromal cells (MSCs) play a crucial role in the regulation of hematopoiesis. These cells affect the process through direct cell–cell contact, as well as releasing various trophic factors and extracellular vehicles (EVs) into the bone marrow microenvironment. MSC-derived EVs (MSC-EVs) are prominent intercellular communication tolls enriched with broad-spectrum bioactive factors such as proteins, cytokines, lipids, miRNAs, and siRNAs. They mimic some effects of MSCs by direct fusion with hematopoietic stem cells (HSC) membranes in the bone marrow (BM), thereby affecting HSC fate. MSC-EVs are attractive scope in cell-free therapy because of their unique capacity to repair BM tissue and regulate proliferation and differentiation of HSCs. These vesicles modulate the immune system responses and inhibit graft-versus-host disease following hematopoietic stem cell transplantation (HSCT). Recent studies have demonstrated that MSC-EVs play an influential role in the BM niches because of their unprecedented capacity to regulate HSC fate. Therefore, the existing paper intends to speculate upon the preconditioned MSC-EVs as a novel approach in HSCT.
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spelling pubmed-91093212022-05-17 Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation Sarvar, Davod Pashoutan Effatpanah, Hosein Akbarzadehlaleh, Parvin Shamsasenjan, Karim Stem Cell Res Ther Review Bone marrow mesenchymal stromal cells (MSCs) play a crucial role in the regulation of hematopoiesis. These cells affect the process through direct cell–cell contact, as well as releasing various trophic factors and extracellular vehicles (EVs) into the bone marrow microenvironment. MSC-derived EVs (MSC-EVs) are prominent intercellular communication tolls enriched with broad-spectrum bioactive factors such as proteins, cytokines, lipids, miRNAs, and siRNAs. They mimic some effects of MSCs by direct fusion with hematopoietic stem cells (HSC) membranes in the bone marrow (BM), thereby affecting HSC fate. MSC-EVs are attractive scope in cell-free therapy because of their unique capacity to repair BM tissue and regulate proliferation and differentiation of HSCs. These vesicles modulate the immune system responses and inhibit graft-versus-host disease following hematopoietic stem cell transplantation (HSCT). Recent studies have demonstrated that MSC-EVs play an influential role in the BM niches because of their unprecedented capacity to regulate HSC fate. Therefore, the existing paper intends to speculate upon the preconditioned MSC-EVs as a novel approach in HSCT. BioMed Central 2022-05-16 /pmc/articles/PMC9109321/ /pubmed/35578300 http://dx.doi.org/10.1186/s13287-022-02875-3 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Sarvar, Davod Pashoutan
Effatpanah, Hosein
Akbarzadehlaleh, Parvin
Shamsasenjan, Karim
Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation
title Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation
title_full Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation
title_fullStr Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation
title_full_unstemmed Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation
title_short Mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation
title_sort mesenchymal stromal cell-derived extracellular vesicles: novel approach in hematopoietic stem cell transplantation
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9109321/
https://www.ncbi.nlm.nih.gov/pubmed/35578300
http://dx.doi.org/10.1186/s13287-022-02875-3
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