Regulation of intracellular iron distribution in K562 human erythroleukemia cells
Journal Article
·
· J. Biol. Chem.; (United States)
OSTI ID:5527757
Following a pulse with 59Fe-transferrin, K562 erythroleukemia cells incorporate a significant amount of 59Fe into ferritin. Conditions or manipulations which alter the supply of iron to cells result in changes in the rate of ferritin biosynthesis with consequent variations in the size of the ferritin pool. Overnight exposure to iron donors such as diferric transferrin or hemin increases the ferritin level 2-4- or 6-8-fold above that of the control, respectively. Treatment with the anti-human transferrin receptor antibody, OKT9 (which reduces the iron uptake by decreasing the number of transferrin receptors) lowers the ferritin level by approximately 70-80% with respect to the control. The fraction of total cell-associated 59Fe (given as a pulse via transferrin) that becomes ferritin bound is proportional to the actual ferritin level and is independent of the instantaneous amount of iron taken up. This has allowed us to establish a curve that correlates different levels of intracellular ferritin with corresponding percentages of incoming iron delivered to ferritin. Iron released from transferrin appears to distribute to ferritin according to a partition function; the entering load going into ferritin is set for a given ferritin level over a wide range of actual amounts of iron delivered.
- Research Organization:
- National Institute of Child Health and Human Development, Bethesda, MD
- OSTI ID:
- 5527757
- Journal Information:
- J. Biol. Chem.; (United States), Journal Name: J. Biol. Chem.; (United States) Vol. 10; ISSN JBCHA
- Country of Publication:
- United States
- Language:
- English
Similar Records
Copper's influence on iron metabolism in K562 cells
Multiple post-transcriptional regulatory mechanisms in ferritin gene expression
Release of iron from the two iron-binding sites of transferrin by cultured human cells: modulation by methylamine
Conference
·
Thu Mar 14 23:00:00 EST 1991
· FASEB Journal (Federation of American Societies for Experimental Biology); (United States)
·
OSTI ID:5213448
Multiple post-transcriptional regulatory mechanisms in ferritin gene expression
Journal Article
·
Tue Feb 28 23:00:00 EST 1989
· Proceedings of the National Academy of Sciences of the United States of America; (USA)
·
OSTI ID:5085066
Release of iron from the two iron-binding sites of transferrin by cultured human cells: modulation by methylamine
Journal Article
·
Tue Jul 02 00:00:00 EDT 1985
· Biochemistry; (United States)
·
OSTI ID:6301354
Related Subjects
550201 -- Biochemistry-- Tracer Techniques
560301* -- Chemicals Metabolism & Toxicology-- Cells-- (-1987)
59 BASIC BIOLOGICAL SCIENCES
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ANIMAL CELLS
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BIOCHEMISTRY
CHEMISTRY
COMPLEXES
DAYS LIVING RADIOISOTOPES
DISEASES
ELEMENTS
EVEN-ODD NUCLEI
FERRITIN
GLOBULINS
GLOBULINS-BETA
HEMIC DISEASES
INTERMEDIATE MASS NUCLEI
IRON
IRON 59
IRON COMPLEXES
IRON ISOTOPES
ISOTOPE APPLICATIONS
ISOTOPES
KINETICS
LEUKEMIA
METABOLISM
METALLOPROTEINS
METALS
MOLECULAR WEIGHT
NEOPLASMS
NUCLEI
ORGANIC COMPOUNDS
PROTEINS
RADIOISOTOPES
TRACER TECHNIQUES
TRANSFERRIN
TRANSITION ELEMENT COMPLEXES
TRANSITION ELEMENTS
TUMOR CELLS
560301* -- Chemicals Metabolism & Toxicology-- Cells-- (-1987)
59 BASIC BIOLOGICAL SCIENCES
63 RADIATION, THERMAL, AND OTHER ENVIRON. POLLUTANT EFFECTS ON LIVING ORGS. AND BIOL. MAT.
ANIMAL CELLS
BETA DECAY RADIOISOTOPES
BETA-MINUS DECAY RADIOISOTOPES
BIOCHEMISTRY
CHEMISTRY
COMPLEXES
DAYS LIVING RADIOISOTOPES
DISEASES
ELEMENTS
EVEN-ODD NUCLEI
FERRITIN
GLOBULINS
GLOBULINS-BETA
HEMIC DISEASES
INTERMEDIATE MASS NUCLEI
IRON
IRON 59
IRON COMPLEXES
IRON ISOTOPES
ISOTOPE APPLICATIONS
ISOTOPES
KINETICS
LEUKEMIA
METABOLISM
METALLOPROTEINS
METALS
MOLECULAR WEIGHT
NEOPLASMS
NUCLEI
ORGANIC COMPOUNDS
PROTEINS
RADIOISOTOPES
TRACER TECHNIQUES
TRANSFERRIN
TRANSITION ELEMENT COMPLEXES
TRANSITION ELEMENTS
TUMOR CELLS