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dc.contributor.authorAnitua Aldekoa, Eduardo
dc.contributor.authorDe la Fuente, María
dc.contributor.authorMuruzabal, Francisco J.
dc.contributor.authorSánchez Ávila, Ronald Mauricio
dc.contributor.authorMerayo Lloves, Jesús
dc.contributor.authorAzkargorta, Mikel
dc.contributor.authorElortza, Felix
dc.contributor.authorOrive Arroyo, Gorka
dc.date.accessioned2018-11-21T09:10:30Z
dc.date.available2018-11-21T09:10:30Z
dc.date.issued2018-10-12
dc.identifier.citationPLOS ONE 13(10) : (2018) // Article ID e0205073es_ES
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/10810/29724
dc.description.abstractPurpose The main objective of this study is to compare the protein expression of human keratocytes treated with Plasma rich in growth factors (PRGF) or autologous serum (AS) and previously induced to myofibroblast by TGF-beta 1 treatment. Methods Blood from healthy donor was collected and processed to obtain AS and PRGF eye drops. Blood derivates were aliquoted and stored at-80 degrees C until use. Keratocyte cells were pretreated for 60 minutes with 2.5 ng/ml TGF-beta 1. After that, cells were treated with PRGF, AS or with TGF-beta 1 (control). To characterize the proteins deregulated after PRGF and AS treatment, a proteomic approach that combines 1D-SDS-PAGE approach followed by LC-MS/MS was carried out. Results Results show a catalogue of key proteins in close contact with a myofibroblastic differentiated phenotype in AS treated-cells, whereas PRGF-treated cells show attenuation on this phenotype. The number of proteins downregulated after PRGF treatment or upregulated in AS-treated cells suggest a close relationship between AS-treated cells and cytoskeletal functions. On the other hand, proteins upregulated after PRGF-treatment or downregulated in AS-treated cells reveal a greater association with processes such as protein synthesis, proliferation and cellular motility. Conclusion This proteomic analysis helps to understand the molecular events underlying AS and PRGF-driven tissue regeneration processes, providing new evidence that comes along with the modulation of TGF-beta 1 activity and the reversion of the myofibroblastic phenotype by PRGF.es_ES
dc.description.sponsorshipThis study was fully supported by BTI Biotechnology Institute, a dental implant company that investigates in the fields of oral implantology and PRGF-Endoret technology. MF and FM received a salary as scientists from BTI Biotechnology Institute. EA is the Scientific Director and president of BTI Biotechnology Institute. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.es_ES
dc.language.isoenges_ES
dc.publisherPublic Library Sciencees_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectocular surface diseaseses_ES
dc.subject3 blood derivativeses_ES
dc.subjectlarge gene listses_ES
dc.subjecteye dropses_ES
dc.subjectin-vitroes_ES
dc.subjectsurgeryes_ES
dc.subjectmyodifferentiationes_ES
dc.subjectproliferationes_ES
dc.subjectregenerationes_ES
dc.subjectfibroblastses_ES
dc.titleDifferential profile of protein expression on human keratocytes treated with autologous serum and plasma rich in growth factors (PRGF)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2018 Anitua et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://journals.plos.org/plosone/article?id=10.1371/journal.pone.0205073es_ES
dc.identifier.doi10.1371/journal.pone.0205073
dc.departamentoesFarmacia y ciencias de los alimentoses_ES
dc.departamentoeuFarmazia eta elikagaien zientziakes_ES


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© 2018 Anitua et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Excepto si se señala otra cosa, la licencia del ítem se describe como © 2018 Anitua et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.