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Biomed Pharmacother ; 96: 1209-1215, 2017 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-29174854

RESUMEN

Osteoarthritis (OA) is a disease with degeneration of articular cartilage and its development and progression is characterized by chondrocyte apoptosis. To examine whether DUSP19 and inhibitor of the JAK2/STAT3 will influence the response of rat chondrocytes cultured with IL-1ß. Dose-response studies were conducted under IL-1ß conditions. In separate experiments, chondrocytes were treated with an appropriate concentration of IL-1ß with either DUSP19-expressing constructs or AG490, whereas chondrocytes were also treated with DUSP19-RNA interference constructs with or without AG490. The expression of DUSP19, apoptosis markers, JAK2/STAT3 and phosphorylation of JAK2/STAT3 was measured by Real-time PCR and/or western blot assay. CCK-8 assay and Annexin V/propidium iodide staining was used to detect chondrocyte viability and apoptosis, respectively. IL-1ß dose-dependently decreased the expression of DUSP19 and the viability of chondrocytes. Chondrocytes with DUSP19 up-regulation inhibited IL-1ß-induced increases in the ratio of p-JAK2/JAK2 and p-STAT3/STAT3 expression as well as cell apoptosis. However, DUSP19 down-regulation mimicked the effect of IL-1ß on JAK2/STAT3 activity and chondrocyte apoptosis. AG490 inhibited JAK2/STAT3 activation as well as apoptosis in chondrocytes induced by IL-1ß or DUSP19 down-regulation, evidenced by decreased expression of Bax, Caspase-3 and increased Bcl-2 expression as well as MMP-3, -9 and -13 expressions. Taken together, our results demonstrate that DUSP19 up-regulation inhibited IL-1ß-induced chondrocytes apoptosis and MMPs expression through inactivating JAK2/STAT3 pathway.


Asunto(s)
Apoptosis/fisiología , Fosfatasas de Especificidad Dual/metabolismo , Interleucina-1beta/metabolismo , Janus Quinasa 2/metabolismo , Metaloproteinasas de la Matriz/metabolismo , Factor de Transcripción STAT3/metabolismo , Transducción de Señal/fisiología , Animales , Cartílago Articular/metabolismo , Células Cultivadas , Condrocitos/metabolismo , Regulación hacia Abajo/fisiología , Masculino , Osteoartritis/metabolismo , Ratas , Ratas Sprague-Dawley , Regulación hacia Arriba/fisiología
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