Journal Article


Micro-RNA and Proteomic Profiles of Plasma-Derived Exosomes from Irradiated Mice Reveal Molecular Changes Preventing Apoptosis in Neonatal Cerebellum

Abstract

Cell communication via exosomes is capable of influencing cell fate in stress situations such as exposure to ionizing radiation. In vitro and in vivo studies have shown that exosomes might play a role in out-of-target radiation effects by carrying molecular signaling mediators of radiation damage, as well as opposite protective functions resulting in resistance to radiotherapy. However, a global understanding of exosomes and their radiation-induced regulation, especially within the context of an intact mammalian organism, has been lacking. In this, in vivo study, we demonstrate that, compared to sham-irradiated (SI) mice, a distinct pattern of proteins and miRNAs is found packaged into circulating plasma exosomes after whole-body and partial-body irradiation (WBI and PBI) with 2 Gy X-rays. A high number of deregulated proteins (59% of WBI and 67% of PBI) was found in the exosomes of irradiated mice. In total, 57 and 13 miRNAs were deregulated in WBI and PBI groups, respectively, suggesting that the miRNA cargo is influenced by the tissue volume exposed to radiation. In addition, five miRNAs (miR-99b-3p, miR-200a-3p, miR-200a, miR-182-5p, miR-182) were commonly overexpressed in the exosomes from the WBI and PBI groups. In this study, particular emphasis was also given to the determination of the in vivo effect of exosome transfer by intracranial injection in the highly radiosensitive neonatal cerebellum at postnatal day 3. In accordance with a major overall anti-apoptotic function of the commonly deregulated miRNAs, here we report that exosomes from plasma of irradiated mice, especially in the case of WBI, prevent radiation-induced apoptosis thus holding promise for exosome-based future therapeutic applications against radiation injury.

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Authors

Pazzaglia, Simonetta
Tanno, Barbara
De Stefano, Ilaria
Giardullo, Paola
Leonardi, Simona
Merla, Caterina
Babini, Gabriele
Tuncay Cagatay, Seda
Mayah, Ammar
Kadhim, Munira
Lyng, Fiona M
von Toerne, Christine
Khan, Zohaib N
Subedi, Prabal
Tapio, Soile
Saran, Anna
Mancuso, Mariateresa

Oxford Brookes departments

School of Biological and Medical Sciences
Faculty of Health, Science and Technology

Dates

Year of publication: 2022
Date of RADAR deposit: 2025-04-29


Creative Commons License This work is licensed under a Creative Commons Attribution 4.0 International License


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