Publication:
Application of low-intensity pulsed therapeutic ultrasound on mesenchymal precursors does not affect their cell properties.

dc.contributor.authorde Lucas, Beatriz
dc.contributor.authorPerez, Laura M.
dc.contributor.authorBernal, Aurora
dc.contributor.authorGalvez, Beatriz G.
dc.date.accessioned2021-09-02T12:51:02Z
dc.date.available2021-09-02T12:51:02Z
dc.date.issued2021-02
dc.description.abstractUltrasound is considered a safe and non-invasive tool in regenerative medicine and has been used in the clinic for more than twenty years for applications in bone healing after the approval of the Exogen device, also known as low-intensity pulsed ultrasound (LIPUS). Beyond its effects on bone health, LIPUS has also been investigated for wound healing of soft tissues, with positive results for various cell processes including cell proliferation, migration and angiogenesis. As LIPUS has the potential to treat chronic skin wounds, we sought to evaluate the effects produced by a conventional therapeutic ultrasound device at low intensities (also considered LIPUS) on the migration capacity of mouse and human skin mesenchymal precursors (s-MPs). Cells were stimulated for 3 days (20 minutes per day) using a traditional ultrasound device with the following parameters: 100 mW/cm2 with 20% duty cycle and frequency of 3 MHz. At the parameters used, ultrasound failed to affect s-MP proliferation, with no evident changes in morphology or cell groupings, and no changes at the cytoskeletal level. Further, the migration and invasion ability of s-MPs were unaffected by the ultrasound protocol, and no major changes were detected in the gene/protein expression of ROCK1, integrin β1, laminin β1, type I collagen and transforming growth factor β1. Finally, RNA-seq analysis revealed that only 10 genes were differentially expressed after ultrasound stimulation. Among them, 5 encode for small nuclear RNAs and 2 encode for proteins belonging to the nuclear pore complex. Considering the results overall, while the viability of s-MPs was not affected by ultrasound stimulation and no changes were detected in proliferation/migration, RNA-seq analysis would suggest that s-MPs do respond to ultrasound. The use of 100 mW/cm2 intensity or conventional therapeutic ultrasound devices might not be optimal for the stimulation the properties of cell populations. Future studies should investigate the potential application of ultrasound using variations of the tested parameters.es_ES
dc.description.peerreviewedes_ES
dc.format.number2es_ES
dc.format.pagee0246261es_ES
dc.format.volume16es_ES
dc.identifier.citationPLoS One. 2021; 16(2):e0246261es_ES
dc.identifier.doi10.1371/journal.pone.0246261es_ES
dc.identifier.issn1932-6203es_ES
dc.identifier.journalPloS onees_ES
dc.identifier.pubmedID33571276es_ES
dc.identifier.urihttp://hdl.handle.net/20.500.12105/13348
dc.language.isoenges_ES
dc.publisherPublic Library of Science (PLOS)es_ES
dc.relation.publisherversionhttps://doi.org/10.1371/journal.pone.0246261es_ES
dc.repisalud.institucionCNICes_ES
dc.repisalud.orgCNICCNIC::Grupos de investigación::Nanomedicina e Imagen Moleculares_ES
dc.rights.accessRightsopen accesses_ES
dc.rights.licenseAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subject.meshUltrasonic Therapyes_ES
dc.subject.meshUltrasonic Waveses_ES
dc.subject.meshAnimalses_ES
dc.subject.meshBlotting, Westernes_ES
dc.subject.meshCell Movementes_ES
dc.subject.meshCytoskeletones_ES
dc.subject.meshHumanses_ES
dc.subject.meshMesenchymal Stem Cellses_ES
dc.subject.meshMicees_ES
dc.subject.meshMicroscopy, Fluorescencees_ES
dc.subject.meshReal-Time Polymerase Chain Reactiones_ES
dc.subject.meshTranscriptomees_ES
dc.subject.meshWound Healinges_ES
dc.titleApplication of low-intensity pulsed therapeutic ultrasound on mesenchymal precursors does not affect their cell properties.es_ES
dc.typejournal articlees_ES
dc.type.hasVersionVoRes_ES
dspace.entity.typePublication
relation.isAuthorOfPublicationced43853-a9b9-4d4c-8e5e-2a32f1205aa3
relation.isAuthorOfPublication194112f8-97ef-4330-b896-f7b517a06583
relation.isAuthorOfPublication4e5e955e-6381-4434-8372-c13f00c2184b
relation.isAuthorOfPublication.latestForDiscoveryced43853-a9b9-4d4c-8e5e-2a32f1205aa3

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