Copyright
©The Author(s) 2021.
World J Hepatol. Oct 27, 2021; 13(10): 1378-1393
Published online Oct 27, 2021. doi: 10.4254/wjh.v13.i10.1378
Published online Oct 27, 2021. doi: 10.4254/wjh.v13.i10.1378
Figure 1 Efficient suppression of hepcidin by higher iron levels.
A: Huh7 cells were treated with 50 μmol/L of FAC, FeCl3, FC, ferrlecit, hemin or FeSO4 for 24 h; B: Murine primary hepatocytes were treated with FAC (50 μmol/L) for 24 h; C: Huh7 cells were treated with FAC (50 μmol/L) in the presence or absence of SIH (100 μmol/L) or Desferal (50 μmol/L) for 24 h. Total RNA was extracted from Huh7 cells or murine primary hepatocytes. Hepcidin mRNA levels were determined by quantitative real-time PCR, normalized to glyceraldehyde 3-phosphate dehydrogenase or hypoxanthine phosphoribosyltransferase or β2mg. Data are presented as mean ± SD. aP < 0.05, bP < 0.001 vs control; dP < 0.001 vs FAC group. FAC: Ferric ammonium citrate; FeCl3: Ferric chloride; FC; Ferric citrate; FeSO4: Ferrous sulfate; SIH: Salicylaldehyde isonicotinoyl hydrazine; GAPDH: Glyceraldehyde 3-phosphate dehydrogenase; β2mg, β2-microglobulin; HPRT: Hypoxanthine phosphoribosyltransferase.
- Citation: Yu LN, Wang SJ, Chen C, Rausch V, Elshaarawy O, Mueller S. Direct modulation of hepatocyte hepcidin signaling by iron. World J Hepatol 2021; 13(10): 1378-1393
- URL: https://www.wjgnet.com/1948-5182/full/v13/i10/1378.htm
- DOI: https://dx.doi.org/10.4254/wjh.v13.i10.1378