dc.creatorBiani, María Celeste
dc.creatorLombardi, Antonella
dc.creatorNorris, Alessandra
dc.creatorBucci, Paula Lorena
dc.creatorla Greca, Alejandro Damián
dc.creatorWaisman, Ariel
dc.creatorMoro, Lucía Natalia
dc.creatorSevlever, Gustavo
dc.creatorMartinetti Montanari, Jorge Anibal
dc.creatorMiriuka, Santiago Gabriel
dc.creatorLuzzani, Carlos Daniel
dc.date.accessioned2022-08-25T13:45:26Z
dc.date.accessioned2022-10-15T00:51:35Z
dc.date.available2022-08-25T13:45:26Z
dc.date.available2022-10-15T00:51:35Z
dc.date.created2022-08-25T13:45:26Z
dc.date.issued2021-09
dc.identifierBiani, María Celeste; Lombardi, Antonella; Norris, Alessandra; Bucci, Paula Lorena; la Greca, Alejandro Damián; et al.; Small extracellular vesicles from iPSC-MSC lose their regenerative potential upon UV-C irradiation; Cold Spring Harbor Laboratory Press; bioRxiv; 9-2021; 1-14
dc.identifier2692-8205
dc.identifierhttp://hdl.handle.net/11336/166563
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4326842
dc.description.abstractMesenchymal Stem Cells derived from induced Pluripotent Stem cells (iPSC-MSC) have become a promising alternative to classical Mesenchymal Stem Cells in regenerative medicine. Their properties -as immunomodulatory and regenerative capacities-are in part due to the secretion of Extracellular Vesicles (EVs). Small EVs (sEVs) with sizes that range from 50 to 120 nm contain proteins, lipids, and nucleic acids that exert a role in cellular communication. Their content will depend on the cell of origin and its physiological state, thus the message they convey might change in response to changes in cellular conditions. In particular, the DNA damage response (DDR) has been reported to modulate sEVs secretion. In this work, we analyze how UV-C radiation upon iPSC-MSC alter sEVs secretion, cargo and bystander effect. Here, we confirm that UV-C radiation causes DDR in a dose dependent manner. In addition, we found that UV-C induced stress did not modulate the expression of genes that participate in sEVs biogenesis pathway. Consequently, we found that the amount of sEVs secreted by radiated and non-irradiated cells remained stable. However, sEVs from radiated cells were unable to promote cell migration in their target cells. Moreover, a label-free proteomic analysis revealed that UV-C induced DDR produces sEVs with an altered cargo, rich in migration-inhibiting proteins, and resulting in a less stromal-oriented repertoire.
dc.languageeng
dc.publisherCold Spring Harbor Laboratory Press
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1101/2021.09.27.461979
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.biorxiv.org/content/10.1101/2021.09.27.461979v1
dc.rightshttps://creativecommons.org/licenses/by-nc/2.5/ar/
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEXOSOMAS
dc.subjectTRPS
dc.titleSmall extracellular vesicles from iPSC-MSC lose their regenerative potential upon UV-C irradiation
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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