The role of NF-§ÜB in SAA-induced peroxisome proliferator-activated receptor ¦Ã activation

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• 作者：Hongzhe Li ^{g0700131@nus.edu.sg} ; Shu Qin Ooi ^{g0601059@nus.edu.sg} ; Chew-Kiat Heng ; ^{paehck@nus.edu.sg}
• 关键词：SAA ; NF-§ÜB ; PPAR¦Ã ; FPRL-1 ; TLR4
• 刊名：Atherosclerosis
• 出版年：2013
• 出版时间：March, 2013
• 年：2013
• 卷：227
• 期：1
• 页码：72-78
• 全文大小：537 K

文摘

Serum amyloid A (SAA) is an acute phase protein whose expression increases markedly during bacterial infection, tissue damage, and inflammation. The potential beneficial roles of SAA include its involvement in the reverse cholesterol transport and possibly extracellular lipid deposition at sites of inflammation and tissue repair. It is an attractive therapeutic target for the treatment of atherosclerosis. Peroxisome proliferator-activated receptor ¦Ã (PPAR¦Ã) plays a major regulatory role in adipogenesis, and the expression of genes involved in lipid metabolism. Activation of PPAR¦Ã leads to multiple changes in gene expression, some of which are believed to be atherogenic while others are antiatherogenic. In this study, we demonstrated that SAA upregulated COX-2 expression and induced PPAR¦Ã activity through NF-§ÜB pathway. The effect of SAA on NF-§ÜB activity is mediated by FPRL-1 and TLR4.