Human isoferritins: organ specific iron and apoferritin distribution
- PMID: 811243
- DOI: 10.1111/j.1365-2141.1975.tb00516.x
Human isoferritins: organ specific iron and apoferritin distribution
Abstract
Ferritins from human liver, spleen, heart, pancreas and kidney were compared by electrophoresis and isoelectric focusing in polyacrylamide gels, by immunodiffusion against antisera to homologous and heterologous ferritin, and in some cases by their cyanogen bromide peptides. All ferritins appeared to consist of a single species on gel electrophoresis with the exception of heart ferritin which separated into two major components. Small differences in electrophoretic mobility were found in all tissue ferritins. By contrast, all tissue ferritins were found to consist of multiple forms when analysed by gel electrofocusing. At least five isoferritins were found in most tissues, several of which were common to most tissues. At least two were common to all tissues. Those ferritins which were most easily distinguishable electrophoretically, e.g. spleen and heart ferritin, showed the greatest differences on gel electrofocusing. The ferritin profile was characteristic of each organ and was reproducible both within individuals and between individual tissues. There were striking differences in the iron content of the various isoferritins within a tissue. Further, the iron content of isoferritins common to more than one tissue varied with the tissue of origin. Some isoferritins in several organs and all of the isoferritins in pancreas appeared to contain little, if any, iron. All five tissue ferritins contained antigenic determinants in common with liver ferritin. However, an additional antigenic determinant was found in liver ferritin which was not detectable in the ferritins from the other organs.
Similar articles
-
Differences in subunit composition and iron content of isoferritins.J Biol Chem. 1975 Jul 25;250(14):5446-9. J Biol Chem. 1975. PMID: 806592
-
Heterogeneity in tissue ferritins displayed by gel electrofocusing.Biochem J. 1974 Sep;141(3):627-32. doi: 10.1042/bj1410627. Biochem J. 1974. PMID: 4478067 Free PMC article.
-
Properties of human tissue isoferritins.Biochem J. 1978 Sep 1;173(3):969-77. doi: 10.1042/bj1730969. Biochem J. 1978. PMID: 708384 Free PMC article.
-
Molecular weight standards for calibration of gel filtration and sodium dodecyl sulfate-polyacrylamide gel electrophoresis: ferritin and apoferritin.Anal Biochem. 1987 Nov 1;166(2):235-45. doi: 10.1016/0003-2697(87)90570-7. Anal Biochem. 1987. PMID: 3324819 Review.
-
Human isoferritins in normal and disease states.Semin Hematol. 1977 Jan;14(1):71-88. Semin Hematol. 1977. PMID: 188201 Review. No abstract available.
Cited by
-
Advances in Ferritin Physiology and Possible Implications in Bacterial Infection.Int J Mol Sci. 2023 Feb 28;24(5):4659. doi: 10.3390/ijms24054659. Int J Mol Sci. 2023. PMID: 36902088 Free PMC article. Review.
-
Mitochondrial Iron Metabolism: The Crucial Actors in Diseases.Molecules. 2022 Dec 21;28(1):29. doi: 10.3390/molecules28010029. Molecules. 2022. PMID: 36615225 Free PMC article. Review.
-
Camel kidney ferritin: isolation and partial characterization.Vet Res Commun. 2000 Jul;24(5):287-97. doi: 10.1023/a:1006455020867. Vet Res Commun. 2000. PMID: 10868547
-
Intravenous iron therapy results in rapid and sustained rise in myocardial iron content through a novel pathway.Eur Heart J. 2024 Nov 8;45(42):4497-4508. doi: 10.1093/eurheartj/ehae359. Eur Heart J. 2024. PMID: 38917062 Free PMC article.
-
Bioactive Molecules Delivery through Ferritin Nanoparticles: Sum Up of Current Loading Methods.Molecules. 2024 Aug 27;29(17):4045. doi: 10.3390/molecules29174045. Molecules. 2024. PMID: 39274893 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources