Autor(es): Domingues, Catarina ; Geraldo, A. Margarida ; Anjo, Sandra I. ; Matos, André ; Almeida, Cláudio ; Caramelo, Inês ; Lopes-da-Silva, José A ; Paiva, Artur ; Carvalho, João ; Neves, Ricardo Pires das ; Manadas, Bruno ; Grãos, Mário
Data: 2020
Identificador Persistente: https://hdl.handle.net/10316/106102
Origem: Estudo Geral - Universidade de Coimbra
Assunto(s): mechanotransduction; Cofilin-1; cytoskeleton; transcription; hUCM-MSCs; proteomics
The mechanical properties of the extracellular environment are interrogated by cells and integrated through mechanotransduction. Many cellular processes depend on actomyosin-dependent contractility, which is influenced by the microenvironment's stiffness. Here, we explored the influence of substrate stiffness on the proteome of proliferating undifferentiated human umbilical cord-matrix mesenchymal stem/stromal cells. The relative abundance of several proteins changed significantly by expanding cells on soft (∼3 kPa) or stiff substrates (GPa). Many such proteins are associated with the regulation of the actin cytoskeleton, a major player of mechanotransduction and cell physiology in response to mechanical cues. Specifically, Cofilin-1 levels were elevated in cells cultured on soft comparing with stiff substrates. Furthermore, Cofilin-1 was de-phosphorylated (active) and present in the nuclei of cells kept on soft substrates, in contrast with phosphorylated (inactive) and widespread distribution in cells on stiff. Soft substrates promoted Cofilin-1-dependent increased RNA transcription and faster RNA polymerase II-mediated transcription elongation. Cofilin-1 is part of a novel mechanism linking mechanotransduction and transcription.
