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Mobilization of liver iron by ferroxidase (ceruloplasmin).
Open accessAbstract
Abstract Iron was mobilized by human ferroxidase from dog liver into the perfusate under simulated physiological conditions. The rate of mobilization was estimated to be 1.8 µm per min per 4.9 µm ferroxidase. Human serum albumin with trace copper was found to be inactive in iron mobilization. The low Km and high k1 values of ferroxidase toward ferrous ion enabled us to deduce that the elimination of free iron in the perfusate by ferroxidase would generate a very steep concentration gradient between iron storage cells and the capillary system. This concentration gradient would promote a rapid iron out-flux from the cells by diffusion.
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“Transport is facilitated by multicopper ferroxidases including the abundant serum protein ceruloplasmin and its membrane-bound intestinal homolog hephaestin.”
From Forging a field: the golden age of iron biology. (2008) · cites this paper as [80]
Citations
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Metadata
- Authors
- Osaki, S., & Johnson, D. A.
- Affiliations
- Florida State University (US)
- Venue
- Journal of Biological Chemistry
- Publisher
- Elsevier BV
- Published
- 1969-10
- Volume
- 244
- Issue
- 20
- Pages
- 5757-5758
- ISSN
- 0021-9258 (ISSN-L)
- OpenAlex
- W1565446694
- Cited by
- 159
- References
- 11
- Citations by year
- 2026: 1 · 2024: 4 · 2023: 1 · 2022: 1 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 2 · 2016: 2 · 2015: 5 · 2014: 7 · 2013: 7 · 2012: 3
- FWCI
- 2.30
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Biological Chemistry (publishedVersion, cc-by)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
- Life Sciences › Neuroscience › Neurology › Neurological diseases and metabolism
- Keywords
- ferroxidase, ceruloplasmin, liver iron, iron mobilization, ferrous iron oxidation, human serum albumin, copper, iron diffusion, canine liver
- MeSH terms
- Animals, Biological Transport, Ceruloplasmin, Dogs, Humans, Iron, Kinetics, Liver, Oxidoreductases, Perfusion, Serum Albumin, Spectrophotometry, Stimulation, Chemical, Time Factors, Transferrin, In Vitro Techniques
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