The DOI matches its Crossref record; 43 of the 43 references it cites were found in a registry or an index.
Characterization of the iron transporter DMT1 (NRAMP2/DCT1) in red blood cells of normal and anemic mk/mkmice
Abstract
Divalent metal transporter 1 (DMT1) is the major transferrin-independent iron uptake system at the apical pole of intestinal cells, but it may also transport iron across the membrane of acidified endosomes in peripheral tissues. Iron transport and expression of the 2 isoforms of DMT1 was studied in erythroid cells that consume large quantities of iron for biosynthesis of hemoglobin. In mk/mk mice that express a loss-of-function mutant variant of DMT1, reticulocytes have a decreased cellular iron uptake and iron incorporation into heme. Interestingly, iron release from transferrin inside the endosome is normal in mk/mkreticulocytes, suggesting a subsequent defect in Fe++ transport across the endosomal membrane. Studies by immunoblotting using membrane fractions from peripheral blood or spleen from normal mice where reticulocytosis was induced by erythropoietin (EPO) or phenylhydrazine (PHZ) treatment suggest that DMT1 is coexpressed with transferrin receptor (TfR) in erythroid cells. Coexpression of DMT1 and TfR in reticulocytes was also detected by double immunofluorescence and confocal microscopy. Experiments with isoform-specific anti-DMT1 antiserum strongly suggest that it is the non–iron-response element containing isoform II of DMT1 that is predominantly expressed by the erythroid cells. As opposed to wild-type reticulocytes, mk/mk reticulocytes express little if any DMT1, despite robust expression of TfR, suggesting a possible effect of the mutation on stability and targeting of DMT1 isoform II in these cells. Together, these results provide further evidence that DMT1 plays a central role in iron acquisition via the transferrin cycle in erythroid cells.
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“Later reports of HH pedigrees also observed this mutation in both alleles of the HFE gene that encodes a tyrosine instead of the normal cysteine at codon 282 (C282Y), as having a prevalence of between 60% and 100% (40, 147, 150).”
From Intracellular iron transport and storage: from molecular mechanisms to health implications (2008) · cites this paper as [40]
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Microcytic anaemia mice have a mutation in Nramp2, a candidate iron transporter gene
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Self-citationI RON R EGULATORY P ROTEINS AND THE M OLECULAR C ONTROL OF M AMMALIAN I RON M ETABOLISM
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Self-citationPonka, P. (1997) · Blood · doi:10.1182/blood.v89.1.1 · Cited by 544
Self-citationCanonne-Hergaux, F., Gruenheid, S., Ponka, P., & Gros, P. (1999) · Blood · doi:10.1182/blood.v93.12.4406 · Cited by 451
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Research works printed but not linked: 1
- Garrick, 1999, The iron transporter DMT1 (or Nramp2 or DCT1) is located mostly in endosomes in normal and belgrade rat reticulocytes. [abstract]., Blood., 94, 403a
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Intracellular iron transport and storage: from molecular mechanisms to health implications
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Nevo, Y., & Nelson, N. (2006) · Biochimica et Biophysica Acta (BBA) - Molecular Cell Research · doi:10.1016/j.bbamcr.2006.05.007 · Cited by 526
NEW INSIGHTS INTO ERYTHROPOIESIS: The Roles of Folate, Vitamin B 12 , and Iron
Koury, M. J., & Ponka, P. (2004) · Annual Review of Nutrition · doi:10.1146/annurev.nutr.24.012003.132306 · Cited by 518
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Metadata
- Authors
- Canonne-Hergaux, F., Zhang, A.-S., Ponka, P., & Gros, P.
- Affiliations
- From the Departments of Biochemistry, Physiology, and Medicine, McGill University, and the Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, QC, Canada.
- Jewish General Hospital (CA)
- Venue
- Blood
- Publisher
- American Society of Hematology
- Published
- 2001-12-15
- Volume
- 98
- Issue
- 13
- Pages
- 3823-3830
- ISSN
- 0006-4971 (ISSN-L)
- 1528-0020
- OpenAlex
- W1984912112
- Cited by
- 169
- References
- 43
- Citations by year
- 2026: 6 · 2025: 6 · 2024: 5 · 2023: 4 · 2022: 5 · 2021: 2 · 2020: 10 · 2019: 3 · 2018: 3 · 2017: 3 · 2016: 3 · 2015: 4 · 2014: 12 · 2013: 6 · 2012: 8
- FWCI
- 3.38
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Blood (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institute of Allergy and Infectious Diseases (AI355237)
- Topics
- Health Sciences › Medicine › Hematology › Iron Metabolism and Disorders
- Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
- Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant Micronutrient Interactions and Effects
- Keywords
- DMT1, iron transport, reticulocytes, erythroid cells, transferrin receptor, heme biosynthesis, reticulocytosis, erythropoiesis, phenylhydrazine, erythropoietin
- MeSH terms
- Solute Carrier Family 11, Member 2, Anemia, Animals, Biological Transport, Erythrocyte Membrane, Erythrocytes, Leukemia, Erythroblastic, Acute, Erythropoietin, Fluorescent Antibody Technique, Cricetinae, Heme, Hemoglobins, Homozygote, Iron, Mice, Mutant Strains, Mutation, Phenylhydrazines, Endosomes, Reticulocytes, Spleen, Transferrin, Tumor Cells, Cultured, Erythroid Precursor Cells, CHO Cells, Reticulocyte Count, Microscopy, Confocal, Protein Isoforms, Cation Transport Proteins, Iron-Binding Proteins, Mice
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