Figure 4
Figure 4. Hepatic overexpression of Hfe does not exacerbate the systemic iron deficiency caused by homozygous loss of Tmprss6. (A-E) Analyses of TS, tissue iron concentrations, and hepatic hepcidin mRNA expression in 8-week-old female Hfe−/− mice harboring 0, 1, or 2 mutant Tmprss6 alleles that are also either null or hemizygous for a liver-specific Hfe transgene. Graphed are mean values obtained from analyses of TS (A), LIC (B), heart nonheme iron concentration (C), hepcidin mRNA expression relative to β-actin (Actb) expression (D), and spleen nonheme iron concentration (E). In panel A, 8 Hfe−/−Tmprss6+/+, 8 Hfe−/−Tmprss6+/−, 6 Hfe−/−Tmprss6−/−, 6 Hfe−/−Tmprss6+/+Hfe tg, 8 Hfe−/−Tmprss6+/−Hfe tg, and 8 Hfe−/−Tmprss6−/−Hfe tg mice were analyzed. In panels B, C, and E, 8 Hfe−/−Tmprss6+/+, 9 Hfe−/−Tmprss6+/−, 7 Hfe−/−Tmprss6−/−, 8 Hfe−/−Tmprss6+/+Hfe tg, 9 Hfe−/−Tmprss6+/−Hfe tg, and 8 Hfe−/−Tmprss6−/−Hfe tg mice were analyzed. In panel D, 7 Hfe−/−Tmprss6+/+, 7 Hfe−/−Tmprss6+/−, 6 Hfe−/−Tmprss6−/−, 6 Hfe−/−Tmprss6+/+Hfe tg, 8 Hfe−/−Tmprss6+/−Hfe tg, and 8 Hfe−/−Tmprss6−/−Hfe tg mice were analyzed. Error bars represent SD. Hfe tg indicates Hfe transgene. *P < .005 compared with Hfe−/−Tmprss6+/+; †P < .05 compared with Hfe−/−Tmprss6−/−; ‡P value not significant compared with Hfe−/−Tmprss6−/−; §P < .05 compared with Hfe−/−Tmprss6+/+Hfe tg; ‖P < .005 compared with Hfe−/−Tmprss6+/+Hfe tg, and ¶P < .05 compared with Hfe−/−Tmprss6+/+ mice.

Hepatic overexpression of Hfe does not exacerbate the systemic iron deficiency caused by homozygous loss of Tmprss6. (A-E) Analyses of TS, tissue iron concentrations, and hepatic hepcidin mRNA expression in 8-week-old female Hfe−/− mice harboring 0, 1, or 2 mutant Tmprss6 alleles that are also either null or hemizygous for a liver-specific Hfe transgene. Graphed are mean values obtained from analyses of TS (A), LIC (B), heart nonheme iron concentration (C), hepcidin mRNA expression relative to β-actin (Actb) expression (D), and spleen nonheme iron concentration (E). In panel A, 8 Hfe−/−Tmprss6+/+, 8 Hfe−/−Tmprss6+/−, 6 Hfe−/−Tmprss6−/−, 6 Hfe−/−Tmprss6+/+Hfe tg, 8 Hfe−/−Tmprss6+/−Hfe tg, and 8 Hfe−/−Tmprss6−/−Hfe tg mice were analyzed. In panels B, C, and E, 8 Hfe−/−Tmprss6+/+, 9 Hfe−/−Tmprss6+/−, 7 Hfe−/−Tmprss6−/−, 8 Hfe−/−Tmprss6+/+Hfe tg, 9 Hfe−/−Tmprss6+/−Hfe tg, and 8 Hfe−/−Tmprss6−/−Hfe tg mice were analyzed. In panel D, 7 Hfe−/−Tmprss6+/+, 7 Hfe−/−Tmprss6+/−, 6 Hfe−/−Tmprss6−/−, 6 Hfe−/−Tmprss6+/+Hfe tg, 8 Hfe−/−Tmprss6+/−Hfe tg, and 8 Hfe−/−Tmprss6−/−Hfe tg mice were analyzed. Error bars represent SD. Hfe tg indicates Hfe transgene. *P < .005 compared with Hfe−/−Tmprss6+/+; †P < .05 compared with Hfe−/−Tmprss6−/−; ‡P value not significant compared with Hfe−/−Tmprss6−/−; §P < .05 compared with Hfe−/−Tmprss6+/+Hfe tg; ‖P < .005 compared with Hfe−/−Tmprss6+/+Hfe tg, and ¶P < .05 compared with Hfe−/−Tmprss6+/+ mice.

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