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Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow

Ionizing radiation (IR)-induced bystander effects contribute to biological responses to radiation, and extracellular vesicles (EVs) play important roles in mediating these effects. In this study we investigated the role of bone marrow (BM)-derived EVs in the bystander transfer of radiation damage. M...

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Autores principales: Kis, Dávid, Csordás, Ilona Barbara, Persa, Eszter, Jezsó, Bálint, Hargitai, Rita, Szatmári, Tünde, Sándor, Nikolett, Kis, Enikő, Balázs, Katalin, Sáfrány, Géza, Lumniczky, Katalin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750882/
https://www.ncbi.nlm.nih.gov/pubmed/35011718
http://dx.doi.org/10.3390/cells11010155
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author Kis, Dávid
Csordás, Ilona Barbara
Persa, Eszter
Jezsó, Bálint
Hargitai, Rita
Szatmári, Tünde
Sándor, Nikolett
Kis, Enikő
Balázs, Katalin
Sáfrány, Géza
Lumniczky, Katalin
author_facet Kis, Dávid
Csordás, Ilona Barbara
Persa, Eszter
Jezsó, Bálint
Hargitai, Rita
Szatmári, Tünde
Sándor, Nikolett
Kis, Enikő
Balázs, Katalin
Sáfrány, Géza
Lumniczky, Katalin
author_sort Kis, Dávid
collection PubMed
description Ionizing radiation (IR)-induced bystander effects contribute to biological responses to radiation, and extracellular vesicles (EVs) play important roles in mediating these effects. In this study we investigated the role of bone marrow (BM)-derived EVs in the bystander transfer of radiation damage. Mice were irradiated with 0.1Gy, 0.25Gy and 2Gy, EVs were extracted from the BM supernatant 24 h or 3 months after irradiation and injected into bystander mice. Acute effects on directly irradiated or EV-treated mice were investigated after 4 and 24 h, while late effects were investigated 3 months after treatment. The acute effects of EVs on the hematopoietic stem and progenitor cell pools were similar to direct irradiation effects and persisted for up to 3 months, with the hematopoietic stem cells showing the strongest bystander responses. EVs isolated 3 months after irradiation elicited no bystander responses. The level of seven microRNAs (miR-33a-3p, miR-140-3p, miR-152-3p, miR-199a-5p, miR-200c-5p, miR-375-3p and miR-669o-5p) was altered in the EVs isolated 24 hour but not 3 months after irradiation. They regulated pathways highly relevant for the cellular response to IR, indicating their role in EV-mediated bystander responses. In conclusion, we showed that only EVs from an early stage of radiation damage could transmit IR-induced bystander effects.
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spelling pubmed-87508822022-01-12 Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow Kis, Dávid Csordás, Ilona Barbara Persa, Eszter Jezsó, Bálint Hargitai, Rita Szatmári, Tünde Sándor, Nikolett Kis, Enikő Balázs, Katalin Sáfrány, Géza Lumniczky, Katalin Cells Article Ionizing radiation (IR)-induced bystander effects contribute to biological responses to radiation, and extracellular vesicles (EVs) play important roles in mediating these effects. In this study we investigated the role of bone marrow (BM)-derived EVs in the bystander transfer of radiation damage. Mice were irradiated with 0.1Gy, 0.25Gy and 2Gy, EVs were extracted from the BM supernatant 24 h or 3 months after irradiation and injected into bystander mice. Acute effects on directly irradiated or EV-treated mice were investigated after 4 and 24 h, while late effects were investigated 3 months after treatment. The acute effects of EVs on the hematopoietic stem and progenitor cell pools were similar to direct irradiation effects and persisted for up to 3 months, with the hematopoietic stem cells showing the strongest bystander responses. EVs isolated 3 months after irradiation elicited no bystander responses. The level of seven microRNAs (miR-33a-3p, miR-140-3p, miR-152-3p, miR-199a-5p, miR-200c-5p, miR-375-3p and miR-669o-5p) was altered in the EVs isolated 24 hour but not 3 months after irradiation. They regulated pathways highly relevant for the cellular response to IR, indicating their role in EV-mediated bystander responses. In conclusion, we showed that only EVs from an early stage of radiation damage could transmit IR-induced bystander effects. MDPI 2022-01-04 /pmc/articles/PMC8750882/ /pubmed/35011718 http://dx.doi.org/10.3390/cells11010155 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kis, Dávid
Csordás, Ilona Barbara
Persa, Eszter
Jezsó, Bálint
Hargitai, Rita
Szatmári, Tünde
Sándor, Nikolett
Kis, Enikő
Balázs, Katalin
Sáfrány, Géza
Lumniczky, Katalin
Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow
title Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow
title_full Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow
title_fullStr Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow
title_full_unstemmed Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow
title_short Extracellular Vesicles Derived from Bone Marrow in an Early Stage of Ionizing Radiation Damage Are Able to Induce Bystander Responses in the Bone Marrow
title_sort extracellular vesicles derived from bone marrow in an early stage of ionizing radiation damage are able to induce bystander responses in the bone marrow
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750882/
https://www.ncbi.nlm.nih.gov/pubmed/35011718
http://dx.doi.org/10.3390/cells11010155
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