دورية أكاديمية

Copyright � The Korean Academy of Medical Sciences ERK-1/-2 and p38 Kinase Oppositely Regulate 15-deoxy- △ 12,14- prostaglandinJ2-Induced PPAR- Activation That Mediates Dedifferentiation But Not Cyclooxygenase-2 Expression in Articular Chondrocytes

التفاصيل البيبلوغرافية
العنوان: Copyright � The Korean Academy of Medical Sciences ERK-1/-2 and p38 Kinase Oppositely Regulate 15-deoxy- △ 12,14- prostaglandinJ2-Induced PPAR- Activation That Mediates Dedifferentiation But Not Cyclooxygenase-2 Expression in Articular Chondrocytes
المؤلفون: Eun-kyung Yoon, Won-kil Lee, Sang-gu Hwang, Song-ja Kim
المساهمون: The Pennsylvania State University CiteSeerX Archives
المصدر: ftp://ftp.ncbi.nlm.nih.gov/pub/pmc/c3/09/J_Korean_Med_Sci_2007_Dec_20_22(6)_1015-1021.tar.gz
سنة النشر: 2007
المجموعة: CiteSeerX
مصطلحات موضوعية: These authors contributed equally to this work
الوصف: Peroxisome proliferator-activated receptor gamma (PPAR-) is a ligand-activated transcription factor and plays an important role in growth, differentiation, and inflammation in different tissues. In this study, we investigated the effects of 15d-PGJ2, a high-affinity ligand of PPAR-, on dedifferentiation and on inflammatory responses such as COX-2 expression and PGE2 production in rabbit articular chondrocytes with a focus on ERK-1/-2, p38 kinase, and PPAR- activation. We report here that 15d-PGJ2 induced dedifferentiation and/or COX-2 expression and subsequent PGE2 production. 15d-PGJ2 treatment stimulated activation of ERK-1/-2, p38 kinase, and PPAR-. Inhibition of ERK-1/-2 with PD98059 recovered 15d-PGJ2-induced dedifferentiation and enhanced PPAR- activation, whereas inhibition of p38 kinase with SB203580 potentiated dedifferentiation and partially blocked PPAR- activation. Inhibition of ERK-1/-2 and p38 kinase abolished 15d-PGJ2-induced COX-2 expression and subsequent PGE2 production. Our findings collectively suggest that ERK-1/-2 and p38 kinase oppositely regulate 15d-PGJ2-induced dedifferentiation through a PPAR--dependent mechanism, whereas COX-2 expression and PGE2
نوع الوثيقة: text
وصف الملف: application/zip
اللغة: English
العلاقة: http://citeseerx.ist.psu.edu/viewdoc/summary?doi=10.1.1.359.3046Test
حقوق: Metadata may be used without restrictions as long as the oai identifier remains attached to it.
رقم الانضمام: edsbas.CB465EB5
قاعدة البيانات: BASE