Leptin enhances CC-chemokine ligand expression in cultured murine macrophage

被引:105
作者
Kiguchi, Norikazu [1 ]
Maeda, Takehiko [1 ]
Kobayashi, Yuka [1 ]
Fukazawa, Yohji [1 ]
Kishioka, Shiroh [1 ]
机构
[1] Wakayama Med Univ, Dept Pharmacol, Wakayama 6410012, Japan
基金
日本学术振兴会;
关键词
Leptin; Chemokine; CCL3; CCL4; CCL5; STAT3; IMMUNE-RESPONSES; INFLAMMATION; ACTIVATION; MEDIATORS; RECEPTOR; INTERLEUKIN-1-BETA; ADIPOKINES; RELEASE; CELLS;
D O I
10.1016/j.bbrc.2009.04.121
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Despite accumulating evidence, the role of leptin in chemokine expression is poorly understood. In this study, we evaluated the effects of leptin on CC-chemokine ligands (CCLs), CCL3, CCL4 and CCL5 gene expression in cultured murine macrophage, J774A.1 cells. Expression of all these CCLs mRNA was gradually increased and significant up-regulation was observed for 3-12 h exposure to leptin (1 mu M). The phosphorylated signal transducer and activator of transcription 3 (pSTAT3) was significantly increased for 5-20 min exposure to leptin, and it was localized in leptin receptor-positive macrophage. Pretreatment with AG490 (100 mu M), a janus kinase 2 (JAK2) inhibitor, significantly suppressed leptin-induced pSTAT3 increases and the up-regulation of CCLs mRNA expression. In conclusion, leptin enhances CCLs expression in cultured murine macrophage, through activation of a JAK2-STAT3 pathway. Therefore, a new paradigm of leptin-mediated chemokine expression may lead to the clarification of complex immune systems in failure. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:311 / 315
页数:5
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