37, 38 All HFE-HH patients had chronic and significant iron overload, and liver biopsies were performed prior to initiation of therapeutic venesection.

Since discovery of the HFE gene, the role of liver biopsy in the diagnosis of HH has diminished considerably, and thus cohorts of patients with complete data including histology and hepatic iron concentrations are less available than in the past. The results outlined in Selleckchem Roscovitine this study confirm several findings from animal models of hemochromatosis. First, BMP6 was up-regulated in iron-loaded patients with HFE-HH compared to controls. As outlined by both Kautz et al.32 and Corradini et al.33, BMP6 expression was induced by iron in both HFE-deficient mice and HFE-wild type mice maintained on an iron-enriched diet, and correlated with increased hepatic iron concentration. Hepatic BMP6 staining displayed a diffuse intracellular pattern and was present in all zones in HFE-HH liver tissue, whereas it was mostly centrilobular and localized to the hepatocyte basolateral membrane in mice with hepatic iron overload. This may reflect the chronicity of iron loading along with the greater extent of iron deposition

seen in these patients.39 Iron excess further induced phosphorylation of Smad1/Smad5/Smad8 and expression of the BMP target genes hepcidin (HAMP) and Id1 in HFE-wild type mice, but importantly, this was not seen in HFE-deficient mice.32, 33 These latter findings were mirrored in the HFE-HH patient cohort, because levels of both hepcidin and Id1 remained similar to controls despite iron-loading and elevated BMP6 levels. A nonsignificant trend toward reduced FG 4592 this website hepcidin expression that was observed in the HFE-HH group was similar to other reports of reduced serum hepcidin levels in HFE-HH, which could be expected to fall further following venesection therapy.40, 41 Moreover, this study (as previously shown in HFE-deficient mice) suggests that induction of BMP6 by iron is not dependent on a functional HFE protein. Expression of Smad4, the central mediator of the BMP signal, was not significantly elevated in the HFE-HH cohort compared to controls. This finding may relate to the abrogated

BMP signal, as levels of Smad1/Smad5/Smad8 phosphorylation were inappropriately low relative to iron burden in the HFE-HH cohort. Furthermore, the pattern of pSmad1/pSmad5/pSmad8 immunostaining evident in HFE-HH liver tissue may be relevant to the impairment of the BMP signal, possibly reflecting local regulatory mechanisms at play. Up-regulation of other BMP target genes, the inhibitory Smad proteins Smad6 and Smad7, was demonstrated in untreated HFE-HH. Indeed, Smad7 expression was seen to follow BMP6 gene expression in mice fed an iron-enriched or iron-deficient diet.29 Smad6 and Smad7 are inhibitors of the transforming growth factor β (TGFβ) family signaling pathway (which includes BMP), and act by preventing phosphorylation of receptor-regulated Smads such as Smad1, Smad5, and Smad8.