Busca avançada
Ano de início
Entree


Modulation of Hyaluronan Synthesis by the Interaction between Mesenchymal Stem Cells and Osteoarthritic Chondrocytes

Texto completo
Autor(es):
Antonioli, Eliane ; Piccinato, Carla A. ; Nader, Helena B. ; Cohen, Moises ; Goldberg, Anna Carla ; Ferretti, Mario
Número total de Autores: 6
Tipo de documento: Artigo Científico
Fonte: STEM CELLS INTERNATIONAL; v. 2015, p. 11-pg., 2015-01-01.
Resumo

Bone marrow mesenchymal stem cells (BM-MSCs) are considered a good source for cellular therapy in cartilage repair. But, their potential to repair the extracellular matrix, in an osteoarthritic environment, is still controversial. In osteoarthritis (OA), anti-inflammatory action and extracellular matrix production are important steps for cartilage healing. This study examined the interaction of BM-MSC and OA-chondrocyte on the production of hyaluronan and inflammatory cytokines in a Transwell system. We compared cocultured BM-MSCs and OA-chondrocytes with the individually cultured controls (monocultures). There was a decrease in BM-MSCs cell count in coculture with OA-chondrocytes when compared to BM-MSCs alone. In monoculture, BM-MSCs produced higher amounts of hyaluronan than OA-chondrocytes and coculture of BM-MSCs with OA-chondrocytes increased hyaluronan production per cell. Hyaluronan synthase-1 mRNA expression was upregulated in BM-MSCs after coculture with OA-chondrocytes, whereas hyaluronidase-1 was downregulated. After coculture, lower IL-6 levels were detected in BM-MSCs compared with OA-chondrocytes. These results indicate that, in response to coculture with OA-chondrocytes, BM-MSCs change their behavior by increasing production of hyaluronan and decreasing inflammatory cytokines. Our results indicate that BM-MSCs per se could be a potential tool for OA regenerative therapy, exerting short-term effects on the local microenvironment even when cell:cell contact is not occurring. (AU)

Processo FAPESP: 12/00831-7 - Condrócitos osteoartríticos e células mesenquimais: relação entre moléculas inflamatórias e da matriz extracelular
Beneficiário:Mario Ferretti Filho
Modalidade de apoio: Auxílio à Pesquisa - Regular