Literature DB >> 8147916

Contrasting uptakes of 59Fe into spleen, liver, kidney and some other soft tissues in normal and hypotransferrinaemic mice. Influence of an antibody against the transferrin receptor.

M W Bradbury1, K Raja, F Ueda.   

Abstract

Uptake of iron-59 from blood into various soft tissues of anaesthetized mice was investigated by continuous intravenous infusion of the radiotracer during 2 hr. The 59Fe was given either as ferrous chloride with ascorbate or as 59Fe-transferrin. Infusions were made into adult mice with and without pretreatment with a monoclonal antibody against transferrin receptors, and into hypotransferrinaemic mice and appropriate controls. In normal mice, 59Fe uptake into spleen was much higher than into other tissues and was 94-96% inhibited by the antibody. Inhibitions due to the antibody were less complete in liver and renal cortex, and there was evidence of some non-transferrin-mediated transport during infusion of 59Fe/ascorbate. In the hypotransferrinaemic mice, tissue uptakes of 59Fe during infusion of 59Fe/ascorbate were enormous, being two to three orders of magnitude greater than in the normal controls. The rank order for size of uptake was liver > renal cortex > pancreas > spleen > other tissues. All tissues examined have a considerable potential capacity for uptake of non-transferrin-bound iron, this being greatest in liver and renal cortex.

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Year:  1994        PMID: 8147916     DOI: 10.1016/0006-2952(94)90407-3

Source DB:  PubMed          Journal:  Biochem Pharmacol        ISSN: 0006-2952            Impact factor:   5.858


  6 in total

Review 1.  The use of hypotransferrinemic mice in studies of iron biology.

Authors:  Julia T Bu; Thomas B Bartnikas
Journal:  Biometals       Date:  2015-02-08       Impact factor: 2.949

2.  The plasma membrane metal-ion transporter ZIP14 contributes to nontransferrin-bound iron uptake by human β-cells.

Authors:  Richard Coffey; Mitchell D Knutson
Journal:  Am J Physiol Cell Physiol       Date:  2016-11-30       Impact factor: 4.249

3.  SLC39A14 Is Required for the Development of Hepatocellular Iron Overload in Murine Models of Hereditary Hemochromatosis.

Authors:  Supak Jenkitkasemwong; Chia-Yu Wang; Richard Coffey; Wei Zhang; Alan Chan; Thomas Biel; Jae-Sung Kim; Shintaro Hojyo; Toshiyuki Fukada; Mitchell D Knutson
Journal:  Cell Metab       Date:  2015-05-28       Impact factor: 27.287

4.  Hepatocyte divalent metal-ion transporter-1 is dispensable for hepatic iron accumulation and non-transferrin-bound iron uptake in mice.

Authors:  Chia-Yu Wang; Mitchell D Knutson
Journal:  Hepatology       Date:  2013-07-01       Impact factor: 17.425

5.  Hepatic transferrin plays a role in systemic iron homeostasis and liver ferroptosis.

Authors:  Yingying Yu; Li Jiang; Hao Wang; Zhe Shen; Qi Cheng; Pan Zhang; Jiaming Wang; Qian Wu; Xuexian Fang; Lingyan Duan; Shufen Wang; Kai Wang; Peng An; Tuo Shao; Raymond T Chung; Shusen Zheng; Junxia Min; Fudi Wang
Journal:  Blood       Date:  2020-08-06       Impact factor: 22.113

6.  Transferrin as a predictor of survival in cirrhosis.

Authors:  André Viveiros; Armin Finkenstedt; Benedikt Schaefer; Mattias Mandorfer; Bernhard Scheiner; Konrad Lehner; Moritz Tobiasch; Thomas Reiberger; Herbert Tilg; Michael Edlinger; Heinz Zoller
Journal:  Liver Transpl       Date:  2018-03       Impact factor: 5.799

  6 in total

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