Stimulation of non-transferrin iron uptake by iron deprivation in K562 cells
Language English Country United States Media print-electronic
Document type Comparative Study, Journal Article, Research Support, Non-U.S. Gov't
PubMed
16904349
DOI
10.1016/j.bcmd.2006.06.004
PII: S1079-9796(06)00156-2
Knihovny.cz E-resources
- MeSH
- K562 Cells MeSH
- Time Factors MeSH
- Cycloheximide pharmacology MeSH
- Humans MeSH
- Tumor Cells, Cultured MeSH
- Iron-Regulatory Proteins antagonists & inhibitors biosynthesis MeSH
- Transferrin metabolism MeSH
- Structure-Activity Relationship MeSH
- Iron metabolism pharmacokinetics MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Comparative Study MeSH
- Names of Substances
- Cycloheximide MeSH
- Iron-Regulatory Proteins MeSH
- Transferrin MeSH
- Iron MeSH
We tested the effect of iron deprivation on the uptake of iron from ferric citrate by human erythroleukemia K562 cells. The iron uptake after 24-h preincubation in defined iron-free medium was approximately 2-3x higher than after the preincubation in control transferrin-containing medium. The preincubation of K562 cells in iron-free medium together with the inhibitor of protein synthesis cycloheximide completely abrogated the stimulation of the iron uptake. The preincubation in iron-free medium resulted in a slight decrease (20%) of DMT1 mRNA level. The level of Dcytb, ferroportin and hephaestin mRNA did not exert any significant change. We also did not find any significant effect on the protein level of DMT1, Dcytb, ferroportin and hephaestin. We conclude that iron deprivation stimulates the uptake of non-transferrin iron in K562 cells and that this stimulation depends on protein synthesis. It seems that the expression of an unknown or seemingly unrelated protein(s) is involved.
References provided by Crossref.org
Expression profiles of iron transport molecules along the duodenum
Role of duodenal iron transporters and hepcidin in patients with alcoholic liver disease