Immunoassay for human serum erythroferrone
Open accessAbstract
Erythroferrone (ERFE) is a glycoprotein hormone secreted by erythroblasts in response to stimulation by erythropoietin (EPO). We previously demonstrated that ERFE messenger RNA expression and serum protein concentration increase in mice subjected to hemorrhage or EPO therapy, that ERFE acts on hepatocytes to suppress hepcidin, and that the resulting decrease in hepcidin augments iron delivery for intensified erythropoiesis. We also showed that ERFE contributes to pathological hepcidin suppression and iron overload in mice with nontransfused β-thalassemia. We now report the development and technical validation of a rabbit monoclonal antibody-based sandwich immunoassay for human ERFE. We use this assay to show that blood loss or EPO administration increases serum ERFE concentrations in humans, and that patients with both nontransfused and transfused β-thalassemia have very high serum ERFE levels, which decrease after blood transfusion. The assay should be useful for human studies of normal and disordered erythropoiesis and its effect on iron homeostasis.
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In non-transfusion-dependent β-thalassemia patients, serum ERFE levels are high, to ensure iron acquisition for the expanded erythropoiesis.
“In non-transfusion-dependent β-thalassemia patients, serum ERFE levels are high,105 to ensure iron acquisition for the expanded erythropoiesis.106”
From Iron metabolism and iron disorders revisited in the hepcidin era (2020) · cites this paper as [105]
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Cites
Identification of erythroferrone as an erythroid regulator of iron metabolism
Kautz, L., Jung, G., Valore, E. V., Rivella, S., Nemeth, E., & Ganz, T. (2014) · Nature Genetics · doi:10.1038/ng.2996 · Cited by 1,127 · see citing works
Self-citationGanz, T. (2013) · Physiological Reviews · doi:10.1152/physrev.00008.2013 · Cited by 1,122 · see citing works
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Iron metabolism and iron disorders revisited in the hepcidin era
Camaschella, C., Nai, A., & Silvestri, L. (2020) · Haematologica · doi:10.3324/haematol.2019.232124 · Cited by 734 · see citing works
Erythroferrone inhibits the induction of hepcidin by BMP6
Arezes, J., Foy, N., McHugh, K., Sawant, A., Quinkert, D., Terraube, V., Brinth, A., Tam, M., LaVallie, E. R., Taylor, S., et al. (2018) · Blood · doi:10.1182/blood-2018-06-857995 · Cited by 277 · see citing works
Erythroferrone structure, function, and physiology: Iron homeostasis and beyond
Srole, D. N., & Ganz, T. (2021) · Journal of Cellular Physiology · doi:10.1002/jcp.30247 · Cited by 155 · see citing works
Self-citationIron metabolism under conditions of ineffective erythropoiesis in β-thalassemia
Rivella, S. (2019) · Blood · doi:10.1182/blood-2018-07-815928 · Cited by 120 · see citing works
A variant erythroferrone disrupts iron homeostasis in <i>SF3B1</i> -mutated myelodysplastic syndrome
Bondu, S., Alary, A.-S., Lefèvre, C., Houy, A., Jung, G., Lefebvre, T., Rombaut, D., Boussaid, I., Bousta, A., Guillonneau, F., et al. (2019) · Science Translational Medicine · doi:10.1126/scitranslmed.aav5467 · Cited by 85 · see citing works
Self-citationCasu, C., Chessa, R., Liu, A., Gupta, R., Drakesmith, H., Fleming, R., Ginzburg, Y. Z., MacDonald, B., & Rivella, S. (2020) · Haematologica · doi:10.3324/haematol.2018.212589 · Cited by 50 · see citing works
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- Authors
- Ganz, T., Jung, G., Naeim, A., Ginzburg, Y., Pakbaz, Z., Walter, P. B., Kautz, L., & Nemeth, E.
- Affiliations
- University of California, Los Angeles (US)
- Department of Medicine and
- Icahn School of Medicine at Mount Sinai (US)
- University of California, Riverside (US)
- University of California, San Francisco (US)
- Université Toulouse III - Paul Sabatier (FR)
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2017-09-07
- Volume
- 130
- Issue
- 10
- Pages
- 1243-1246
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- PMC
- PMC5606005
- OpenAlex
- W2738794292
- Cited by
- 125
- References
- 2
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 7 · 2023: 13 · 2022: 10 · 2021: 27 · 2020: 19 · 2019: 22 · 2018: 16 · 2017: 1
- FWCI
- 12.22
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Blood (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- HAL (submittedVersion)
- Funders
- National Institutes of Health (UL1TR001881)
- National Heart, Lung, and Blood Institute (U54HL119893)
- National Institute of Diabetes and Digestive and Kidney Diseases (R01DK065029, R01DK107309, P30DK041301, R01DK095112, R01DK107670)
- National Center for Advancing Translational Sciences
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Medicine › Hematology › Erythropoietin and Anemia Treatment
- Health Sciences › Medicine › Genetics › Hemoglobinopathies and Related Disorders
- Keywords
- erythroferrone, sandwich immunoassay, monoclonal antibodies, serum protein measurement, erythropoietin, hepcidin, iron homeostasis, erythropoiesis, beta-thalassemia, blood transfusion, hemorrhage, iron overload
- MeSH terms
- Adult, Aged, Blood Donors, Erythropoiesis, Humans, Immunoassay, Male, Middle Aged, beta-Thalassemia, Peptide Hormones, Young Adult, Hepcidins
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