Literature DB >> 807277

Red cell iron uptake in hereditary microcytic anemia.

J A Edwards, J E Hoke.   

Abstract

The iron uptake in vitro of red cells from mice with hereditary microcytic anemia (gene symbol mk) was studied to examine the hypothesis of a generalized impairment of cellular iron uptake in this conidition. Reticulocyte-rich red cells from anemic (mk/mk) and acutely bled normal (+/+) mice were incubated in 59Fe-labeled mouse plasma and the radioiron uptake measured. The 59Fe uptake of the mk/mk and +/+ cells was related in the same way to the reticulocyte concentration, the duration of incubation, and the percentage saturation of the plasma iron-binding capacity. However, under the same conditions, the iron uptake of red cells from normal (+/+) mice was greater than that by red cells from anemic (mk/mk) mice. Furthermore, the cellular loss of radioiron on exposure to EDTA was greater for the mk/mk red cells, although the proportion of the radioiron taken up that was incorporated into heme was the same for mk/mk and +/+ red cells. These results support the hypothesis of a generalized impairment of cellular iron uptake in hereditary microcytic anemia and suggest that there might be a defect in red cell receptor sites for transferrin in this condition.

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Year:  1975        PMID: 807277

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  9 in total

Review 1.  Manganese transport and trafficking: lessons learned from Saccharomyces cerevisiae.

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Journal:  Eukaryot Cell       Date:  2005-07

2.  Nramp2 is mutated in the anemic Belgrade (b) rat: evidence of a role for Nramp2 in endosomal iron transport.

Authors:  M D Fleming; M A Romano; M A Su; L M Garrick; M D Garrick; N C Andrews
Journal:  Proc Natl Acad Sci U S A       Date:  1998-02-03       Impact factor: 11.205

3.  nm1054: a spontaneous, recessive, hypochromic, microcytic anemia mutation in the mouse.

Authors:  Robert S Ohgami; Dean R Campagna; Brendan Antiochos; Emily B Wood; John J Sharp; Jane E Barker; Mark D Fleming
Journal:  Blood       Date:  2005-06-30       Impact factor: 22.113

4.  Localisation of divalent metal transporter 1 (DMT1) to the microvillus membrane of rat duodenal enterocytes in iron deficiency, but to hepatocytes in iron overload.

Authors:  D Trinder; P S Oates; C Thomas; J Sadleir; E H Morgan
Journal:  Gut       Date:  2000-02       Impact factor: 23.059

5.  Alternative splicing regulates the subcellular localization of divalent metal transporter 1 isoforms.

Authors:  Mitsuaki Tabuchi; Naotaka Tanaka; Junko Nishida-Kitayama; Hiroshi Ohno; Fumio Kishi
Journal:  Mol Biol Cell       Date:  2002-12       Impact factor: 4.138

Review 6.  Placental iron transport: The mechanism and regulatory circuits.

Authors:  Veena Sangkhae; Elizabeta Nemeth
Journal:  Free Radic Biol Med       Date:  2018-07-05       Impact factor: 7.376

7.  Augmented internalisation of ferroportin to late endosomes impairs iron uptake by enterocyte-like IEC-6 cells.

Authors:  Phillip S Oates; Carla Thomas
Journal:  Pflugers Arch       Date:  2005-06-17       Impact factor: 3.657

Review 8.  Inherited metabolic disease in laboratory animals: a review.

Authors:  G Bulfield
Journal:  J Inherit Metab Dis       Date:  1980       Impact factor: 4.982

9.  The iron transport protein NRAMP2 is an integral membrane glycoprotein that colocalizes with transferrin in recycling endosomes.

Authors:  S Gruenheid; F Canonne-Hergaux; S Gauthier; D J Hackam; S Grinstein; P Gros
Journal:  J Exp Med       Date:  1999-03-01       Impact factor: 14.307

  9 in total

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