Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 1 de 1
Filtrar
Añadir filtros








Intervalo de año
1.
Experimental & Molecular Medicine ; : 534-544, 2004.
Artículo en Inglés | WPRIM | ID: wpr-13638

RESUMEN

During chronic inflammatory response, mono- cytes/macrophages produce 92-kDa matrix metalloproteinase-9 (MMP-9), which may contribute to their extravasation, migration and tissue remodeling. Activation of peroxisome proliferator- activated factor receptor-gamma (PPAR-gamma) has been shown to inhibit MMP-9 activity. To evaluate whether ox-LDL, a PPAR-gamma activator, inhibits PMA-induced MMP-9 expression and activity, and if so, whether CD36 and PPAR-gamma are involved in this process, we investigated the effect of ox-LDL on MMP-9 expression and activity in PMA-activated human monocytic cell line U937. PMA-induced MMP-9 expression and activity were suppressed by the treatment with ox-LDL (50 micrigram/ml) or PPAR-gamma activators such as troglitazone (5 micrometer), ciglitazone (5 micrometer), and 15d- PGJ2 (1 micrometer) for 24 h. This ox-LDL or PPAR-gamma activator-mediated inhibition of micrometer P-9 activity was diminished by the pre-treatment of cells with a blocking antibody to CD36, or PGF2a (0.3 micrometer), which is a PPAR-gamma inhibitor, as well as overexpression of a dominant-negative form of CD36. Taken together, these results suggest that ox-LDL suppresses PMA-induced MMP-9 expression and activity through CD36-mediated activation of PPAR-gamma.


Asunto(s)
Humanos , Anticuerpos Bloqueadores/farmacología , Antígenos CD36/inmunología , Células Cultivadas , Cromanos/farmacología , Metaloproteinasa 9 de la Matriz/antagonistas & inhibidores , Lipoproteínas LDL/farmacología , Monocitos/efectos de los fármacos , FN-kappa B/antagonistas & inhibidores , PPAR gamma/metabolismo , Prostaglandina D2/análogos & derivados , ARN Mensajero/análisis , Acetato de Tetradecanoilforbol/antagonistas & inhibidores , Tiazolidinedionas/farmacología , Transcripción Genética/efectos de los fármacos
SELECCIÓN DE REFERENCIAS
DETALLE DE LA BÚSQUEDA