Cytokine-mediated modulation of leptin and adiponectin secretion during in vitro adipogenesis:: Evidence that tumor necrosis factor-α- and interleukin-1β-treated human preadipocytes are potent leptin producers

Over the last decade, compelling evidence has been presented that cytokines affect adipocyte tissue formation and function. In this study we explored the effect of pro-inflammatory (i.e. interleukin (IL)-1 beta, IL-6, interferon (IFN)-gamma, and tumor necrosis factor (TNF)-alpha) versus anti-inflammatory cytokines (i.e. IL-4, IL-10, and transforming growth factor (TGF)-beta(1)) on leptin and adiponectin secretion during in vitro human adipogenesis. Confirmative to previous reports, conversion of precursor preadipocytes into mature adipocytes was completely inhibited upon exposure to TNF-alpha, IL-1 beta, IFN-gamma, or TGF-beta(1). Hence, all these anti-adipogenic cytokines prevented release of adipocyte-specific adiponectin. IFN-gamma also strongly reduced leptin production (>= 85%). However, TNF-alpha, IL-1 beta, and TGF-beta(1) stimulated leptin production from preadipocytes in the absence of mature adipocytes (20.6 +/- 5.4 ng/ml, 100.8 +/- 18.2 ng/ml, and 5.4 +/- 0.4 ng/ml, respectively, compared to 6.6 +/- 0.8 ng/ml in control adipocyte cultures on day 2 1; n = 4). IL-4, IL-6 and IL-10 did not, or only slightly, affect adipocyte differentiation and their hormonal secretion. In conclusion, adiponectin and leptin are both synthesized by adipocytes, whereas leptin is also produced by preadipocytes upon TNF-alpha or IL-1 beta stimulation. These data suggest that preadipocytes could contribute more to total circulating leptin levels than has been previously considered, especially in diseased conditions were these pro-inflammatory factors play a prominent role. (c) 2005 Elsevier Ltd. All rights reserved.