Barley β-glucan accelerates wound healing by favoring migration versus proliferation of human dermal fibroblasts

β-Glucans are considered candidates for the medication in different human pathologies. In this work, we have purified β-glucan from a selected barley line and tested their effects in primary human dermal fibroblasts. Unexpectedly, we have observed that this compound promoted a short-transitory proli...

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Detalhes bibliográficos
Autores: Pérez Fusté, Noel, Guasch Vallés, Marta, Guillén, Pere, Anerillas Aljama, Carlos, Cemeli, Tània, Pedraza González, Neus, Ferrezuelo, Francisco, Encinas Martín, Mario, Moralejo Vidal, Mª Angeles, Garí Marsol, Eloi
Tipo de documento: artigo
Estado:Versão publicada
Data de publicação:2019
País:España
Recursos:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repositório:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:10459.1/65923
Acesso em linha:https://doi.org/10.1016/j.carbpol.2019.01.090
http://hdl.handle.net/10459.1/65923
Access Level:Acceso aberto
Palavra-chave:Barley β-glucan
Retinoblastoma
Proliferation arrest
Migration
Descrição
Resumo:β-Glucans are considered candidates for the medication in different human pathologies. In this work, we have purified β-glucan from a selected barley line and tested their effects in primary human dermal fibroblasts. Unexpectedly, we have observed that this compound promoted a short-transitory proliferation arrest at 24 h after its addition on the medium. We have determined that this transitory arrest was dependent on the cell-cycle regulator protein Retinoblastoma. Moreover, dermal fibroblasts increase their migration capacities at 24 h after barley β-glucan addition. Also, we have described that barley β-glucan strongly reduced the ability of fibroblasts to attach and to spread on cell plates. Our data indicates that barley β-glucan signal induces an early response in HDF cells favoring migration versus proliferation. This feature is consistent with our observation that the topical addition of our barley β-glucan in vivo accelerates the wound closure in mouse skin.