10889193

Source:http://linkedlifedata.com/resource/pubmed/id/10889193

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0033618, umls-concept:C0033640, umls-concept:C0040162, umls-concept:C0085862, umls-concept:C0086982, umls-concept:C0229535, umls-concept:C0242275, umls-concept:C0378503, umls-concept:C0851285, umls-concept:C1299583, umls-concept:C1549571, umls-concept:C1608386
pubmed:issue	41
pubmed:dateCreated	2000-11-13
pubmed:abstractText	Intracellular iron homeostasis is regulated, in part, by interactions between iron-regulatory proteins (IRP1 and IRP2) and iron-responsive elements (IREs) in ferritin and transferrin receptor mRNAs. In addition to iron, cellular oxidative stress induced by H(2)O(2), nitric oxide, and hypoxia, and hormonal activation by thyroid hormone and erythropoeitin have each been shown to regulate IRP binding to IREs. Hormonal signals, in particular mediated through protein kinase C (PKC), play a central role in the modulation of IRP/IRE interactions since phorbol esters were shown to activate IRP binding (Eisenstein, R. S., Tuazon, P. T., Schalinske, K. L., Anderson, S. A., and Traugh, J. A. (1993) J. Biol. Chem. 268, 27363-27370). In pituitary thyrotrophs (TtT97), we found that thyrotropin releasing hormone (TRH) and epidermal growth factor (EGF) increased IRP binding to a ferritin IRE, dependent on PKC and mitogen-activated protein kinase (MAPK) activity. In contrast, TRH and EGF decreased IRP binding in pituitary lactotrophs (GH3), despite activation of PKC and MAPK. IRP1 and IRP2 levels remained constant and IRP2 binding was predominant throughout. TRH and EGF markedly decreased IRP binding in MAPK kinase inhibitor-treated GH3 cells, whereas, they increased IRP binding in phosphatase inhibitor-treated GH3 cells. IRE-dependent CAT reporter translational expression closely reflected IRP binding to the ferritin IRE in both GH3 and TtT97 cells. Interestingly, ferritin protein levels were regulated similarly by TRH in both cell lines. These data link two different cell receptor systems to common signaling pathways that regulate IRP binding and ferritin expression. Remarkably, for TRH and EGF, these effects may be PKC-dependent or -independent determined by the cell type.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985121R
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Epidermal Growth Factor, http://linkedlifedata.com/resource/pubmed/chemical/Ferritins, http://linkedlifedata.com/resource/pubmed/chemical/Iron, http://linkedlifedata.com/resource/pubmed/chemical/Iron Regulatory Protein 1, http://linkedlifedata.com/resource/pubmed/chemical/Iron Regulatory Protein 2, http://linkedlifedata.com/resource/pubmed/chemical/Iron-Regulatory Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Iron-Sulfur Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Mitogen-Activated Protein Kinases, http://linkedlifedata.com/resource/pubmed/chemical/Phosphoprotein Phosphatases, http://linkedlifedata.com/resource/pubmed/chemical/Protein Kinase C, http://linkedlifedata.com/resource/pubmed/chemical/RNA, http://linkedlifedata.com/resource/pubmed/chemical/RNA-Binding Proteins, http://linkedlifedata.com/resource/pubmed/chemical/Tetradecanoylphorbol Acetate, http://linkedlifedata.com/resource/pubmed/chemical/Thyrotropin-Releasing Hormone
pubmed:status	MEDLINE
pubmed:month	Oct
pubmed:issn	0021-9258
pubmed:author	pubmed-author:LeedmanP JPJ, pubmed-author:RogersJ TJT, pubmed-author:ThomsonA MAM
pubmed:issnType	Print
pubmed:day	13
pubmed:volume	275
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	31609-15
pubmed:dateRevised	2009-11-19
pubmed:meshHeading	pubmed-meshheading:10889193-Animals, pubmed-meshheading:10889193-Epidermal Growth Factor, pubmed-meshheading:10889193-Ferritins, pubmed-meshheading:10889193-Genes, Reporter, pubmed-meshheading:10889193-Homeostasis, pubmed-meshheading:10889193-Iron, pubmed-meshheading:10889193-Iron Regulatory Protein 1, pubmed-meshheading:10889193-Iron Regulatory Protein 2, pubmed-meshheading:10889193-Iron-Regulatory Proteins, pubmed-meshheading:10889193-Iron-Sulfur Proteins, pubmed-meshheading:10889193-MAP Kinase Signaling System, pubmed-meshheading:10889193-Mitogen-Activated Protein Kinases, pubmed-meshheading:10889193-Phosphoprotein Phosphatases, pubmed-meshheading:10889193-Pituitary Gland, pubmed-meshheading:10889193-Protein Binding, pubmed-meshheading:10889193-Protein Kinase C, pubmed-meshheading:10889193-RNA, pubmed-meshheading:10889193-RNA-Binding Proteins, pubmed-meshheading:10889193-Rats, pubmed-meshheading:10889193-Response Elements, pubmed-meshheading:10889193-Signal Transduction, pubmed-meshheading:10889193-Tetradecanoylphorbol Acetate, pubmed-meshheading:10889193-Thyrotropin-Releasing Hormone, pubmed-meshheading:10889193-Tumor Cells, Cultured, pubmed-meshheading:10889193-Up-Regulation
pubmed:year	2000
pubmed:articleTitle	Thyrotropin-releasing hormone and epidermal growth factor regulate iron-regulatory protein binding in pituitary cells via protein kinase C-dependent and -independent signaling pathways.
pubmed:affiliation	Laboratory for Cancer Medicine and University Department of Medicine, University of Western Australia, Western Australian Institute for Medical Research, Royal Perth Hospital, Perth, Western Australia 6000, Australia.
pubmed:publicationType	Journal Article, Research Support, U.S. Gov't, P.H.S., Research Support, Non-U.S. Gov't