Iron chelation-induced senescence-like growth arrest in hepatocyte cell lines:: association of transforming growth factor β1 (TGF-β1)-mediated p27Kip1 expression

Iron is essential for cellular proliferation in all organisms. When deprived of iron, the growth of cells is invariably inhibited. However, the mechanism involved remains largely unclear. In the present study, we have observed that subcytotoxic concentrations of desferroxamine mesylate (DFO), an iron chelator, specifically inhibited the transition from G(1) to S-phase of Chang cells, a hepatocyte cell line. This was accompanied by the appearance of senescent biomarkers, such as enlarged and flattened cell morphology, senescence-associated beta-galactosidase activity and reduced expression of poly(ADP-ribose) polymerase. Concomitantly, p27(Kip1) (where Kip is kinase-inhibitory protein) was induced markedly, whereas other negative cell-cycle regulators, such as p21(Cip1) (where Cip is cyclin-dependent kinase-interacting protein), p15(INK4B) and p16(INK4A) (Where INK is inhibitors of cyclin-dependent kinase 4), were not, implying its association in the G(1) arrest. Furthermore, the induction of p27(Kip1) was accompanied by an increased level of transforming growth factor beta1 (TGF-beta1) mRNA. When neutralized with an anti-(TGF-beta1) antibody, p27(Kip1) induction was completely abolished, indicating that TGF-beta1 is the major inducer of p27(Kip1). Finally, DFO-induced senescence-like arrest was found to be independent of p53, since cell-cycle arrest was still observed with two p53-negative cell lines, Huh7 and Hep3B cells. In conclusion, DFO induced senescence-like G, arrest in hepatocyte cell lines and this was associated with the induction of p27(Kip1) through TGF-beta1, but was independent of p53.