Effect of mesenchymal stem cells combined with chondroitin sulfate in an in vitro model of osteoarthritis

[EN] Osteoarthritis (OA) is a degenerative joint disease affecting the whole joint structure. The specific mol- ecules responsible for the inflammatory processes involved in the development of OA have been the focus of many studies. Adipose tissue-derived mesenchymal stem cells (ASCs) constitute a p...

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Detalles Bibliográficos
Autores: Pérez Castrillo, Saúl, González Fernández, María Luisa, Álvarez Suárez, Jessica, Sánchez Lázaro, Jaime, Esteban Blanco, Marta, Gutiérrez Velasco, Laura, González Cubero, Elsa, Villar Suárez, María Vega
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2021
País:España
Institución:Universidad de León
Repositorio:BULERIA. Repositorio Institucional de la Universidad de León
OAI Identifier:oai:buleria.unileon.es:10612/24866
Acceso en línea:https://hdl.handle.net/10612/24866
Access Level:acceso abierto
Palabra clave:Medicina. Salud
Mesenchymal stem cells
Chondroitin sulfate
Osteoarthritis
3212 Salud Publica
Descripción
Sumario:[EN] Osteoarthritis (OA) is a degenerative joint disease affecting the whole joint structure. The specific mol- ecules responsible for the inflammatory processes involved in the development of OA have been the focus of many studies. Adipose tissue-derived mesenchymal stem cells (ASCs) constitute a promising cell-based therapy which could be used as an alternative to or in combination with drug therapies. Chondroitin sulfate (CS) plays a protec- tive role in the joint by decreasing concentrations of pro-inflammatory cytokines and therefore has an important part in moderating chondrocyte metabolism. The aim of this study is to use an in vitro model of OA to evaluate the combined effectiveness of CS and ASCs as a treatment. We give a detailed discussion of the roles of cytokines and other key molecules involved in OA. In addition, we report the effects of treating inflamed chondrocytes with ASCs and CS on the expression of specific cartilage genes. Findings show that both treatments reduced expression of all genes associated with the pro-inflammatory cytokines we analyzed. However, we saw no increase in the expression of the specific genes encoding for cartilage matrix proteins, such as collagen type II and aggrecan. This study shows the effectiveness of combining ASCs and CS in the treatment of OA