The Regulation of Cellular Iron Metabolism
While iron is an essential trace element required by nearly all living organisms, deficiencies or excesses can lead to pathological conditions such as iron deficiency anemia or hemochromatosis, respectively. A decade has passed since the discovery of the hemochromatosis gene, HFE, and our understand...
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Veröffentlicht in: | Critical reviews in clinical laboratory sciences 2007-01, Vol.44 (5-6), p.413-459 |
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description | While iron is an essential trace element required by nearly all living organisms, deficiencies or excesses can lead to pathological conditions such as iron deficiency anemia or hemochromatosis, respectively. A decade has passed since the discovery of the hemochromatosis gene, HFE, and our understanding of hereditary hemochromatosis (HH) and iron metabolism in health and a variety of diseases has progressed considerably. Although HFE-related hemochromatosis is the most widespread, other forms of HH have subsequently been identified. These forms are not attributed to mutations in the HFE gene but rather to mutations in genes involved in the transport, storage, and regulation of iron. This review is an overview of cellular iron metabolism and regulation, describing the function of key proteins involved in these processes, with particular emphasis on the liver's role in iron homeostasis, as it is the main target of iron deposition in pathological iron overload. Current knowledge on their roles in maintaining iron homeostasis and how their dysregulation leads to the pathogenesis of HH are discussed. |
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G. ; Graham, Ross M. ; Trinder, Debbie ; Olynyk, John K.</creator><creatorcontrib>Chua, Anita C. G. ; Graham, Ross M. ; Trinder, Debbie ; Olynyk, John K.</creatorcontrib><description>While iron is an essential trace element required by nearly all living organisms, deficiencies or excesses can lead to pathological conditions such as iron deficiency anemia or hemochromatosis, respectively. A decade has passed since the discovery of the hemochromatosis gene, HFE, and our understanding of hereditary hemochromatosis (HH) and iron metabolism in health and a variety of diseases has progressed considerably. Although HFE-related hemochromatosis is the most widespread, other forms of HH have subsequently been identified. These forms are not attributed to mutations in the HFE gene but rather to mutations in genes involved in the transport, storage, and regulation of iron. This review is an overview of cellular iron metabolism and regulation, describing the function of key proteins involved in these processes, with particular emphasis on the liver's role in iron homeostasis, as it is the main target of iron deposition in pathological iron overload. Current knowledge on their roles in maintaining iron homeostasis and how their dysregulation leads to the pathogenesis of HH are discussed.</description><identifier>ISSN: 1040-8363</identifier><identifier>EISSN: 1549-781X</identifier><identifier>DOI: 10.1080/10408360701428257</identifier><identifier>PMID: 17943492</identifier><identifier>CODEN: CRCLBH</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Anemia, Iron-Deficiency - metabolism ; Animals ; Antimicrobial Cationic Peptides - metabolism ; Biological Transport ; Cation Transport Proteins - metabolism ; Ceruloplasmin - metabolism ; GPI-Linked Proteins ; Hemochromatosis - genetics ; Hemochromatosis Protein ; hepcidin ; Hepcidins ; HFE ; Histocompatibility Antigens Class I - metabolism ; Humans ; Intestinal Absorption ; iron ; Iron - metabolism ; Iron Metabolism Disorders - genetics ; Iron Overload - metabolism ; Iron, Dietary - pharmacokinetics ; Iron-Binding Proteins - genetics ; Iron-Binding Proteins - metabolism ; liver ; Liver - metabolism ; Membrane Proteins - metabolism ; Mutation - genetics ; Receptors, Transferrin - deficiency ; Receptors, Transferrin - genetics ; Receptors, Transferrin - metabolism ; Transferrin - deficiency ; Transferrin - genetics ; Transferrin - metabolism ; transferrin receptors</subject><ispartof>Critical reviews in clinical laboratory sciences, 2007-01, Vol.44 (5-6), p.413-459</ispartof><rights>2007 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2007</rights><rights>Copyright Taylor & Francis Ltd. 2007</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c431t-9cdb4b4bd2497773c0207cb193f40b320a6a1366c50a806580304358dd8921bc3</citedby><cites>FETCH-LOGICAL-c431t-9cdb4b4bd2497773c0207cb193f40b320a6a1366c50a806580304358dd8921bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/10408360701428257$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/10408360701428257$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,59620,59726,60409,60515,61194,61229,61375,61410</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/17943492$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Chua, Anita C. G.</creatorcontrib><creatorcontrib>Graham, Ross M.</creatorcontrib><creatorcontrib>Trinder, Debbie</creatorcontrib><creatorcontrib>Olynyk, John K.</creatorcontrib><title>The Regulation of Cellular Iron Metabolism</title><title>Critical reviews in clinical laboratory sciences</title><addtitle>Crit Rev Clin Lab Sci</addtitle><description>While iron is an essential trace element required by nearly all living organisms, deficiencies or excesses can lead to pathological conditions such as iron deficiency anemia or hemochromatosis, respectively. A decade has passed since the discovery of the hemochromatosis gene, HFE, and our understanding of hereditary hemochromatosis (HH) and iron metabolism in health and a variety of diseases has progressed considerably. Although HFE-related hemochromatosis is the most widespread, other forms of HH have subsequently been identified. These forms are not attributed to mutations in the HFE gene but rather to mutations in genes involved in the transport, storage, and regulation of iron. This review is an overview of cellular iron metabolism and regulation, describing the function of key proteins involved in these processes, with particular emphasis on the liver's role in iron homeostasis, as it is the main target of iron deposition in pathological iron overload. Current knowledge on their roles in maintaining iron homeostasis and how their dysregulation leads to the pathogenesis of HH are discussed.</description><subject>Anemia, Iron-Deficiency - metabolism</subject><subject>Animals</subject><subject>Antimicrobial Cationic Peptides - metabolism</subject><subject>Biological Transport</subject><subject>Cation Transport Proteins - metabolism</subject><subject>Ceruloplasmin - metabolism</subject><subject>GPI-Linked Proteins</subject><subject>Hemochromatosis - genetics</subject><subject>Hemochromatosis Protein</subject><subject>hepcidin</subject><subject>Hepcidins</subject><subject>HFE</subject><subject>Histocompatibility Antigens Class I - metabolism</subject><subject>Humans</subject><subject>Intestinal Absorption</subject><subject>iron</subject><subject>Iron - metabolism</subject><subject>Iron Metabolism Disorders - genetics</subject><subject>Iron Overload - metabolism</subject><subject>Iron, Dietary - pharmacokinetics</subject><subject>Iron-Binding Proteins - genetics</subject><subject>Iron-Binding Proteins - metabolism</subject><subject>liver</subject><subject>Liver - metabolism</subject><subject>Membrane Proteins - metabolism</subject><subject>Mutation - genetics</subject><subject>Receptors, Transferrin - deficiency</subject><subject>Receptors, Transferrin - genetics</subject><subject>Receptors, Transferrin - metabolism</subject><subject>Transferrin - deficiency</subject><subject>Transferrin - genetics</subject><subject>Transferrin - metabolism</subject><subject>transferrin receptors</subject><issn>1040-8363</issn><issn>1549-781X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNp9kF1LwzAYhYMobk5_gDdSvPBCqL75aJugNzL8GEwEmeBdSNPUdbTNTFpk_97IBkNFyUW-nnM470HoGMMFBg6XGBhwmkIGmBFOkmwHDXHCRJxx_LobzuE_DgAdoAPvFwCQJoTtowHOBKNMkCE6n81N9Gze-lp1lW0jW0ZjU9fh6qKJCw-PplO5rSvfHKK9UtXeHG32EXq5u52NH-Lp0_1kfDONNaO4i4UuchZWQZjIsoxqIJDpHAtaMsgpAZUqTNNUJ6B4CMSBAqMJLwouCM41HaGzte_S2ffe-E42ldchlGqN7b1MOQOMGQ3g6Q9wYXvXhmyShMlTJkQaILyGtLPeO1PKpasa5VYSg_xqUf5qMWhONsZ93phiq9jUFoDrNVC1pXWN-rCuLmSnVrV1pVOtrryk__lffZPPjaq7uVbObCf4W_0JcjaOUA</recordid><startdate>20070101</startdate><enddate>20070101</enddate><creator>Chua, Anita C. G.</creator><creator>Graham, Ross M.</creator><creator>Trinder, Debbie</creator><creator>Olynyk, John K.</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>S0X</scope><scope>7X8</scope></search><sort><creationdate>20070101</creationdate><title>The Regulation of Cellular Iron Metabolism</title><author>Chua, Anita C. G. ; Graham, Ross M. ; Trinder, Debbie ; Olynyk, John K.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c431t-9cdb4b4bd2497773c0207cb193f40b320a6a1366c50a806580304358dd8921bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Anemia, Iron-Deficiency - metabolism</topic><topic>Animals</topic><topic>Antimicrobial Cationic Peptides - metabolism</topic><topic>Biological Transport</topic><topic>Cation Transport Proteins - metabolism</topic><topic>Ceruloplasmin - metabolism</topic><topic>GPI-Linked Proteins</topic><topic>Hemochromatosis - genetics</topic><topic>Hemochromatosis Protein</topic><topic>hepcidin</topic><topic>Hepcidins</topic><topic>HFE</topic><topic>Histocompatibility Antigens Class I - metabolism</topic><topic>Humans</topic><topic>Intestinal Absorption</topic><topic>iron</topic><topic>Iron - metabolism</topic><topic>Iron Metabolism Disorders - genetics</topic><topic>Iron Overload - metabolism</topic><topic>Iron, Dietary - pharmacokinetics</topic><topic>Iron-Binding Proteins - genetics</topic><topic>Iron-Binding Proteins - metabolism</topic><topic>liver</topic><topic>Liver - metabolism</topic><topic>Membrane Proteins - metabolism</topic><topic>Mutation - genetics</topic><topic>Receptors, Transferrin - deficiency</topic><topic>Receptors, Transferrin - genetics</topic><topic>Receptors, Transferrin - metabolism</topic><topic>Transferrin - deficiency</topic><topic>Transferrin - genetics</topic><topic>Transferrin - metabolism</topic><topic>transferrin receptors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Chua, Anita C. 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Although HFE-related hemochromatosis is the most widespread, other forms of HH have subsequently been identified. These forms are not attributed to mutations in the HFE gene but rather to mutations in genes involved in the transport, storage, and regulation of iron. This review is an overview of cellular iron metabolism and regulation, describing the function of key proteins involved in these processes, with particular emphasis on the liver's role in iron homeostasis, as it is the main target of iron deposition in pathological iron overload. Current knowledge on their roles in maintaining iron homeostasis and how their dysregulation leads to the pathogenesis of HH are discussed.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>17943492</pmid><doi>10.1080/10408360701428257</doi><tpages>47</tpages></addata></record> |
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subjects | Anemia, Iron-Deficiency - metabolism Animals Antimicrobial Cationic Peptides - metabolism Biological Transport Cation Transport Proteins - metabolism Ceruloplasmin - metabolism GPI-Linked Proteins Hemochromatosis - genetics Hemochromatosis Protein hepcidin Hepcidins HFE Histocompatibility Antigens Class I - metabolism Humans Intestinal Absorption iron Iron - metabolism Iron Metabolism Disorders - genetics Iron Overload - metabolism Iron, Dietary - pharmacokinetics Iron-Binding Proteins - genetics Iron-Binding Proteins - metabolism liver Liver - metabolism Membrane Proteins - metabolism Mutation - genetics Receptors, Transferrin - deficiency Receptors, Transferrin - genetics Receptors, Transferrin - metabolism Transferrin - deficiency Transferrin - genetics Transferrin - metabolism transferrin receptors |
title | The Regulation of Cellular Iron Metabolism |
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