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Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin

BACKGROUND: Multipotent mesenchymal stromal cells (MSCs) are precursors of various cell types. Through soluble factors, direct cell–cell interactions and other intercellular communication mechanisms such as extracellular vesicles and tunneling nanotubes, MSCs support tissue homeostasis. In the bone...

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Autores principales: Deniz, Ilker A., Karbanová, Jana, Wobus, Manja, Bornhäuser, Martin, Wimberger, Pauline, Kuhlmann, Jan Dominik, Corbeil, Denis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926842/
https://www.ncbi.nlm.nih.gov/pubmed/36788616
http://dx.doi.org/10.1186/s12964-022-01028-6
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author Deniz, Ilker A.
Karbanová, Jana
Wobus, Manja
Bornhäuser, Martin
Wimberger, Pauline
Kuhlmann, Jan Dominik
Corbeil, Denis
author_facet Deniz, Ilker A.
Karbanová, Jana
Wobus, Manja
Bornhäuser, Martin
Wimberger, Pauline
Kuhlmann, Jan Dominik
Corbeil, Denis
author_sort Deniz, Ilker A.
collection PubMed
description BACKGROUND: Multipotent mesenchymal stromal cells (MSCs) are precursors of various cell types. Through soluble factors, direct cell–cell interactions and other intercellular communication mechanisms such as extracellular vesicles and tunneling nanotubes, MSCs support tissue homeostasis. In the bone marrow microenvironment, they promote hematopoiesis. The interaction between MSCs and cancer cells enhances the cancer and metastatic potential. Here, we have demonstrated that plastic-adherent MSCs isolated from human bone marrow generate migrasomes, a newly discovered organelle playing a role in intercellular communication. RESULTS: Migrasomes are forming a network with retraction fibers behind the migrating MSCs or surrounding them after membrane retraction. The MSC markers, CD44, CD73, CD90, CD105 and CD166 are present on the migrasome network, the latter being specific to migrasomes. Some migrasomes harbor the late endosomal GTPase Rab7 and exosomal marker CD63 indicating the presence of multivesicular bodies. Stromal cell-derived factor 1 (SDF-1) was detected in migrasomes, suggesting that they play a chemoattractant role. Co-cultures with KG-1a leukemic cells or primary CD34(+) hematopoietic progenitors revealed that MSC-associated migrasomes attracted them, a process intercepted by the addition of AMD3100, a specific CXCR4 receptor inhibitor, or recombinant SDF-1. An antibody directed against CD166 reduced the association of hematopoietic cells and MSC-associated migrasomes. In contrast to primary CD34(+) progenitors, leukemic cells can take up migrasomes. CONCLUSION: Overall, we described a novel mechanism used by MSCs to communicate with cells of hematopoietic origin and further studies are needed to decipher all biological aspects of migrasomes in the healthy and transformed bone marrow microenvironment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-022-01028-6.
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spelling pubmed-99268422023-02-15 Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin Deniz, Ilker A. Karbanová, Jana Wobus, Manja Bornhäuser, Martin Wimberger, Pauline Kuhlmann, Jan Dominik Corbeil, Denis Cell Commun Signal Research BACKGROUND: Multipotent mesenchymal stromal cells (MSCs) are precursors of various cell types. Through soluble factors, direct cell–cell interactions and other intercellular communication mechanisms such as extracellular vesicles and tunneling nanotubes, MSCs support tissue homeostasis. In the bone marrow microenvironment, they promote hematopoiesis. The interaction between MSCs and cancer cells enhances the cancer and metastatic potential. Here, we have demonstrated that plastic-adherent MSCs isolated from human bone marrow generate migrasomes, a newly discovered organelle playing a role in intercellular communication. RESULTS: Migrasomes are forming a network with retraction fibers behind the migrating MSCs or surrounding them after membrane retraction. The MSC markers, CD44, CD73, CD90, CD105 and CD166 are present on the migrasome network, the latter being specific to migrasomes. Some migrasomes harbor the late endosomal GTPase Rab7 and exosomal marker CD63 indicating the presence of multivesicular bodies. Stromal cell-derived factor 1 (SDF-1) was detected in migrasomes, suggesting that they play a chemoattractant role. Co-cultures with KG-1a leukemic cells or primary CD34(+) hematopoietic progenitors revealed that MSC-associated migrasomes attracted them, a process intercepted by the addition of AMD3100, a specific CXCR4 receptor inhibitor, or recombinant SDF-1. An antibody directed against CD166 reduced the association of hematopoietic cells and MSC-associated migrasomes. In contrast to primary CD34(+) progenitors, leukemic cells can take up migrasomes. CONCLUSION: Overall, we described a novel mechanism used by MSCs to communicate with cells of hematopoietic origin and further studies are needed to decipher all biological aspects of migrasomes in the healthy and transformed bone marrow microenvironment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12964-022-01028-6. BioMed Central 2023-02-14 /pmc/articles/PMC9926842/ /pubmed/36788616 http://dx.doi.org/10.1186/s12964-022-01028-6 Text en © The Author(s) 2023 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 Research
Deniz, Ilker A.
Karbanová, Jana
Wobus, Manja
Bornhäuser, Martin
Wimberger, Pauline
Kuhlmann, Jan Dominik
Corbeil, Denis
Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin
title Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin
title_full Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin
title_fullStr Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin
title_full_unstemmed Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin
title_short Mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin
title_sort mesenchymal stromal cell-associated migrasomes: a new source of chemoattractant for cells of hematopoietic origin
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9926842/
https://www.ncbi.nlm.nih.gov/pubmed/36788616
http://dx.doi.org/10.1186/s12964-022-01028-6
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