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The diffusion of normal skin wound myofibroblast-derived microvesicles differs according to matrix composition.
Arif, Syrine; Larochelle, Sébastien; Trudel, Benjamin; Gounou, Céline; Bordeleau, François; Brisson, Alain R; Moulin, Véronique J.
Afiliación
  • Arif S; Faculté de Médecine Université Laval Quebec Quebec City Canada.
  • Larochelle S; Centre de Recherche du CHU de Québec-Université Laval Quebec Quebec City Canada.
  • Trudel B; Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX Quebec Quebec City Canada.
  • Gounou C; Centre de Recherche du CHU de Québec-Université Laval Quebec Quebec City Canada.
  • Bordeleau F; Centre de Recherche en Organogénèse Expérimentale de l'Université Laval/LOEX Quebec Quebec City Canada.
  • Brisson AR; Faculté de Médecine Université Laval Quebec Quebec City Canada.
  • Moulin VJ; Centre de Recherche du CHU de Québec-Université Laval Quebec Quebec City Canada.
J Extracell Biol ; 3(1): e131, 2024 Jan.
Article en En | MEDLINE | ID: mdl-38938680
ABSTRACT
Microvesicles (MVs) are a subtype of extracellular vesicles that can transfer biological information over long distances, affecting normal and pathological processes including skin wound healing. However, the diffusion of MVs into tissues can be impeded by the extracellular matrix (ECM). We investigated the diffusion of dermal wound myofibroblast-derived MVs into the ECM by using hydrogels composed of different ECM molecules such as fibrin, type III collagen and type I collagen that are present during the healing process. Fluorescent MVs mixed with hydrogels were employed to detect MV diffusion using fluorometric methods. Our results showed that MVs specifically bound type I collagen and diffused freely out of fibrin and type III collagen. Further analysis using flow cytometry and specific inhibitors revealed that MVs bind to type I collagen via the α2ß1 integrin. These data demonstrate that MV transport depends on the composition of the wound environment.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Extracell Biol Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: J Extracell Biol Año: 2024 Tipo del documento: Article