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Cited by 372

The DOI matches its Crossref record; 11 of the 11 references it cites were found in a registry or an index.

Hemojuvelin is essential for dietary iron sensing, and its mutation leads to severe iron overload

Open access
Niederkofler, V.·2005·Journal of Clinical Investigation

Abstract

Iron homeostasis plays a critical role in many physiological processes, notably synthesis of heme proteins. Dietary iron sensing and inflammation converge in the control of iron absorption and retention by regulating the expression of hepcidin, a regulator of the iron exporter ferroportin. Human mutations in the glycosylphosphatidylinositol-anchored protein hemojuvelin (HJV; also known as RGMc and HFE2) cause juvenile hemochromatosis, a severe iron overload disease, but the way in which HJV intersects with the iron regulatory network has been unclear. Here we show that, within the liver, mouse Hjv is selectively expressed by periportal hepatocytes and also that Hjv-mutant mice exhibit iron overload as well as a dramatic decrease in hepcidin expression. Our findings define a key role for Hjv in dietary iron sensing and also reveal that cytokine-induced inflammation regulates hepcidin expression through an Hjv-independent pathway.

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Crossref · 10.1172/jci25683

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Metadata

Authors
Niederkofler, V.
Venue
Journal of Clinical Investigation
Published
2005-08-01
Volume
115
Issue
8
Pages
2180-2186
ISSN
0021-9738 (ISSN-L)
OpenAlex
W2142833570
Cited by
372
References
11
FWCI
14.99
Type
journal article
Language
en
Open access
bronze

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Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.