Human MRCKalpha is regulated by cellular iron levels and interferes with transferrin iron uptake
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
20188707
DOI
10.1016/j.bbrc.2010.02.148
PII: S0006-291X(10)00382-7
Knihovny.cz E-resources
- MeSH
- Myotonin-Protein Kinase MeSH
- Endocytosis MeSH
- Endosomes enzymology MeSH
- HeLa Cells MeSH
- Humans MeSH
- RNA, Small Interfering genetics MeSH
- Protein Serine-Threonine Kinases genetics metabolism MeSH
- Receptors, Transferrin metabolism MeSH
- RNA Interference MeSH
- Transferrin metabolism MeSH
- Iron metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- CDC42BPA protein, human MeSH Browser
- Myotonin-Protein Kinase MeSH
- RNA, Small Interfering MeSH
- Protein Serine-Threonine Kinases MeSH
- Receptors, Transferrin MeSH
- Transferrin MeSH
- Iron MeSH
Myotonic dystrophy kinase-related Cdc42-binding kinase alpha (MRCKalpha, formally known as CDC42BPA) is a serine/threonine kinase that can regulate actin/myosin assembly and activity. Recently, it has been shown that it possesses a functional iron responsive element (IRE) in the 3'-untranslated region (UTR) of its mRNA, suggesting that it may be involved in iron metabolism. Here we report that MRCKalpha protein expression is also regulated by iron levels; MRCKalpha colocalizes with transferrin (Tf)-loaded transferrin receptors (TfR), and attenuation of MRCKalpha expression by a short hairpin RNA silencing construct leads to a significant decrease in Tf-mediated iron uptake. Our results thus indicate that MRCKalpha takes part in Tf-iron uptake, probably via regulation of Tf-TfR endocytosis/endosome trafficking that is dependent on the cellular cytoskeleton. Regulation of the MRCKalpha activity by intracellular iron levels could thus represent another molecular feedback mechanism cells could use to finely tune iron uptake to actual needs.
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