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©2012 Baishideng Publishing Group Co.
World J Hepatol. Apr 27, 2012; 4(4): 119-128
Published online Apr 27, 2012. doi: 10.4254/wjh.v4.i4.119
Published online Apr 27, 2012. doi: 10.4254/wjh.v4.i4.119
Figure 3 Redox signaling in iron (Fe)-induced liver preconditioning is elicited by the cellular labile Fe pool triggering nuclear factor-erythroid 2, signal transducer and activator of transcription 3, and nuclear factor-κB activation and iron-regulatory protein / iron-responsive element post-transcriptional up-regulation with antioxidant and acute-phase responses.
BMP: Bone morphogenetic protein; Ft: Ferritin; H2O2: Hydrogen peroxide; HO•: hydroxyl radical; IL-6: Interleukin-6; IRE: Iron-responsive element; IRP: Iron-regulatory protein; Nrf2: Nuclear factor-erythroid 2 related factor 2; ROS: Reactive oxygen species; STAT3: Signal transducer and activator of transcription 3; O2−: Superoxide radical; Tf: Transferring; TNF-α: Tumor necrosis factor-α.
- Citation: Fernández V, Tapia G, Videla LA. Recent advances in liver preconditioning: Thyroid hormone, n-3 long-chain polyunsaturated fatty acids and iron. World J Hepatol 2012; 4(4): 119-128
- URL: https://www.wjgnet.com/1948-5182/full/v4/i4/119.htm
- DOI: https://dx.doi.org/10.4254/wjh.v4.i4.119