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

Abstract 

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-kB) 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-kB, 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.

Abbreviations: JAK, Janus kinase, MAPK, mitogen-activated protein kinase, NF-kB, nuclear factor-kappa B, PI3K, phosphatidylinositol 3-kinase, STAT, signal trasducers and activator of transcription

Keywords: Leptin, Apoptosis, Dendritic cell