Literature DB >> 3182815

Hepatocytes and reticulocytes have different mechanisms for the uptake of iron from transferrin.

K Thorstensen1.   

Abstract

The uptake of iron from transferrin by isolated rat hepatocytes and rat reticulocytes has been compared. The results show the following. 1) Reticulocytes and hepatocytes express plasma membrane NADH:ferricyanide oxidoreductase activity. The activity, expressed per 10(6) cells, is approximately 60-fold higher in the hepatocyte than in the reticulocyte. 2) Hepatocyte plasma membrane NADH:ferricyanide oxidoreductase activity and uptake of iron from transferrin are stimulated by low oxygen concentration and inhibited by iodoacetate. In reticulocytes, similar changes are seen in NADH:ferricyanide oxidoreductase activity, but not on iron uptake. 3) Ferricyanide inhibits the uptake of iron from transferrin by hepatocytes, but has no effect on iron uptake by reticulocytes. 4) Perturbants of endocytosis and endosomal acidification have no inhibitory effect on hepatocyte iron uptake, but inhibit reticulocyte iron uptake. 5) Hydrophilic iron chelators effectively inhibit hepatocyte iron uptake, but have no effect on reticulocyte iron uptake. Hydrophobic iron chelators generally inhibit both hepatocyte and reticulocyte iron uptake. 6) Divalent metal cations with ionic radii similar to or less than the ferrous iron ion are effective inhibitors of hepatocyte iron uptake with no effect on reticulocyte iron uptake. The results are compatible with hepatocyte uptake of iron from transferrin by a reductive process at the cell surface and reticulocyte iron uptake by receptor-mediated endocytosis.

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Year:  1988        PMID: 3182815

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  12 in total

1.  Effect of ascorbate in the reduction of transferrin-associated iron in endocytic vesicles.

Authors:  A Escobar; V Gaete; M T Núñez
Journal:  J Bioenerg Biomembr       Date:  1992-04       Impact factor: 2.945

Review 2.  The role of transferrin in the mechanism of cellular iron uptake.

Authors:  K Thorstensen; I Romslo
Journal:  Biochem J       Date:  1990-10-01       Impact factor: 3.857

3.  Molecular mechanisms of non-transferrin-bound and transferring-bound iron uptake in primary hippocampal neurons.

Authors:  Changyi Ji; Daniel J Kosman
Journal:  J Neurochem       Date:  2015-03-10       Impact factor: 5.372

4.  Identification and characterization of the iron compounds in bone marrow by means of Mössbauer spectrometry.

Authors:  C M Jumpertz; J N Rimbert
Journal:  Biometals       Date:  1993       Impact factor: 2.949

5.  Cholesterol movement between the plasma membrane and the cholesteryl ester droplets of cultured Leydig tumour cells.

Authors:  L Nagy; D A Freeman
Journal:  Biochem J       Date:  1990-11-01       Impact factor: 3.857

6.  Kinetics of iron passage through subcellular compartments of rabbit reticulocytes.

Authors:  J A Watkins; M T Nunez; V Gaete; O Alvarez; J Glass
Journal:  J Membr Biol       Date:  1991-01       Impact factor: 1.843

Review 7.  Transferrin and transferrin receptor function in brain barrier systems.

Authors:  T Moos; E H Morgan
Journal:  Cell Mol Neurobiol       Date:  2000-02       Impact factor: 5.046

8.  Iron reverses impermeable chelator inhibition of DNA synthesis in CCl 39 cells.

Authors:  F J Alcain; H Löw; F L Crane
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-16       Impact factor: 11.205

9.  The mammalian transferrin-independent iron transport system may involve a surface ferrireductase activity.

Authors:  I Jordan; J Kaplan
Journal:  Biochem J       Date:  1994-09-15       Impact factor: 3.857

10.  Isolated rat hepatocytes acquire iron from lactoferrin by endocytosis.

Authors:  D D McAbee
Journal:  Biochem J       Date:  1995-10-15       Impact factor: 3.857

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