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. Author manuscript; available in PMC: 2015 Jul 31.
Published in final edited form as: Trends Parasitol. 2013 Apr 16;29(5):220–227. doi: 10.1016/j.pt.2013.03.006

Table 1.

Regulation of iron regulatory proteins in macrophagesa

stimuli iron heme inflammation pRBCs Salmonella Refs
hepcidin no effect [36] n.a. ↑ transcriptional e.g., IL-6, LPS [36, 37] ↑ transcriptional [38, 76] ↑ transcriptional [47]

ferroportin ↑ post-transcriptional [78] ↑ transcriptional [26, 79] ↓posttranslational by hepcidin [36, 39] n.a. ↑ transcriptional /no effect [44, 47]
↑ transcriptional [36] ↓ transcriptional LPS, IFNγ, TNFα

H- ferritin ↑ post-transcriptional [78] ↑ transcriptional [26] ↑transcriptional? n.a. ↑ transcriptional /no effect [44, 47]

HO-1 n.a. ↑ transcriptional [26, 79] ↑ IL- 10, not LPS [80] ↑ transcriptional [63] ↑ transcriptional [44, 47]

DMT-1 ↓posttranslational [78] no effect [81] ↑ transcriptional LPS, IFNγ, TNFα [39] n.a. ↑ transcriptional [44, 47]
↑ transcriptional? [36]

Nramp-1 n.a. ↑ transcriptional [81] ↑ transcriptional LPS [82] n.a. n.a.
a

Overview of how iron regulatory proteins of macrophages (vertical column) are affected by various components related to malaria infection (iron, heme, inflammatory stimuli, pRBCs) as well as by Salmonella. The consequence of these alterations is discussed in Figure 1.

Abbreviations: LPS, lipopolysaccharide; TNFα, tumor necrosis factor α; IFNγ, interferon γ; n.a., no reports available.