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Por favor, use este identificador para citar o enlazar este ítem: http://uvadoc.uva.es/handle/10324/22096
Título: Human corneal fibroblast migration and ECM synthesis during stromal repair: Role played by PDGF-BB, bFGF, and TGFβ1 (HCFs migration and ECM synthesis during stromal repair: GFs effects)
Autor: Gallego Muñoz, Patricia
Ibares Frías, Lucía
Garrote Adrados, José Antonio
Valsero Blanco, María Cruz
Cantalapiedra Rodríguez, Roberto
Merayo Lloves, Jesús
Martínez García, M. Carmen
Año del Documento: 2016
Editorial: Wiley
Descripción: Producción Científica
Documento Fuente: J Tissue Eng Regen Med. 2016 Nov 15
Resumen: The development of treatments that modulate corneal wound healing to avoid fibrosis during tissue repair is important for the restoration of corneal transparency after an injury. To date, few studies have studied the influence of growth factors (GFs) on human corneal fibroblast (HCF) expression of extracellular matrix (ECM) proteins such as collagen types I and III, proteoglycans such as perlecan, or proteins implicated in cellular migration such as α5β1-integrin and syndecan-4. Using in vitro HCFs, we developed a mechanical wound model to study the influence of the GFs basic fibroblast growth factor (bFGF), platelet-derived growth factor (PDGF-BB), and transforming growth factor beta 1 (TGFβ1) on ECM protein production and cellular migration. Our results show that mechanical wounding provokes the autocrine release of bFGF and TGFβ1 at different time points during the wound closure. The HCF response to PDGF-BB was a rapid closure due to fast cellular migration associated with a high focal adhesion replacement and a high expression of collagen and proteoglycans, producing a non-fibrotic healing. bFGF stimulated non-fibrotic ECM production and limited the migration process. Finally, TGFβ1 induced expression of the fibrotic markers collagen type III and α5β1 integrin, and it inhibited cellular migration due to the formation of focal adhesions with a low turnover rate. The novel in vitro HCF mechanical wound model can be used to understand the role played by GFs in human corneal repair. The model can also be used to test the effects of different treatments aimed at improving the healing process.
Materias (normalizadas): Córnea - Enfermedades
ISSN: 1932-6254
Revisión por Pares: SI
DOI: 10.1002/term.2360
Idioma: eng
URI: http://uvadoc.uva.es/handle/10324/22096
Derechos: info:eu-repo/semantics/openAccess
Aparece en las colecciones:DEP05 - Artículos de revista

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