Leptin exerts an anti-apoptotic effect on human dendritic cells via the PI3K-Akt signaling pathway

被引:69
|
作者
Mattioli, Benedetta [1 ]
Giordani, Luciana [1 ]
Quaranta, Maria Giovanna [1 ]
Viora, Marina [1 ]
机构
[1] Ist Super Sanita, Dept Therapeut Res & Med Evaluat, I-00161 Rome, Italy
关键词
Leptin; Apoptosis; Dendritic cell; SURVIVAL; ACTIVATION; LYMPHOCYTES; EXPRESSION; KINETICS;
D O I
10.1016/j.febslet.2009.02.029
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Leptin is an adipocyte-derived hormone/cytokine that modulates immune responses. It induces functional and morphological changes in human dendritic cells (DCs), licensing them towards Th1 priming and promoting DC survival. Here we found that leptin protects DCs from spontaneous, UVB and H2O2-induced apoptosis, by triggering the activation of nuclear factor-kappa B (NF-kappa B) and a parallel up-regulation of bcl-2 and bcl-XL gene expression and Akt activation. We found that leptin activates the PI3K-Akt signaling pathway as demonstrated by the suppression of the effect of leptin on DC survival by wortmannin and API-2, which suppress the leptin-induced activation of Akt, NF-kappa B, bcl-2, bcl-XL and protection from apoptosis. These results provide insights on the immunoregulatory function of leptin, supporting a potential application in immunotherapeutic approaches. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.
引用
收藏
页码:1102 / 1106
页数:5
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