7- to 5.6-fold) as compared with control mice (3.1- to 3.5-fold) ( Table 2). Hepcidin is constitutively

produced by the liver to maintain plasma iron levels within a narrow physiologic range. To do so it senses a variety of physiologic and pathophysiologic stimuli that tend to alter blood iron levels, and responds by inhibiting ferroportin, the main iron-exporter in mammals.33 In this study we showed that hepcidin is regulated transcriptionally also by gluconeogenic signals through PPARGC1A/CREBH. Induction of this regulatory pathway in a classic model of insulin resistance/activated gluconeogenesis, ie, starvation, leads to tissue iron retention Dabrafenib and circulatory iron deficiency. Hypoferremia is clearly secondary to increased tissue iron retention after hepcidin induction and not to reduced food iron intake because it still is preserved in mice premaintained on an iron-deprived diet (Figure 2). Activation of hepcidin and perturbation of iron homeostasis during starvation-induced gluconeogenesis seem to represent a general defensive response in rodents because it was found in other tested mouse strains. However, differences in terms of the time course of hepcidin induction and the

extent of iron RAD001 order status modifications were detected clearly among various starving mice strains. This could be explained by the fact that both the gluconeogenic response/gluconeogenic gene expression and iron status/iron gene expression may vary DCLK1 appreciably

among mouse strains, as also documented by the significantly higher expression of the Pck1 gene in C57BL/6 mice (an optimal mouse model for studying gluconeogenesis/insulin resistance 34 and 35 and the model that most closely parallels the gluconeogenic response to starvation seen in human beings) as compared with 129S2, BALB/c, and Creb3l3 null mice (which actually display a mixed genetic background of 129S1, 129X1, C57BL/6, FVB/N). A close look at the time course induction of Pck1/Hamp ( Figure 1A and B) and Ppargc1a/Creb3l3 RNAs ( Figure 3A and B) suggests that the initial 5-hour burst of Hamp transcription largely depends on increased Creb3l3 expression. Later, the increase in Ppargc1A expression likely sustains hepcidin transcription by enhancing and further stabilizing CREBH binding on the Hamp promoter ( Figure 4F, ChIP study). We were able to reproduce the effect of starvation in vitro, in a hepatoma cell line and cultured primary hepatocytes, using different gluconeogenic stimuli ( Figure 4). However, the Hamp gene response to gluconeogenic signals in primary hepatocytes was lower than in hepatoma cells.