Role of Ceruloplasmin in Cellular Iron Uptake
Individuals with hereditary ceruloplasmin (Cp) deficiency have profound iron accumulation in most tissues, which suggests that Cp is important for normal release of cellular iron. Here, in contrast to expectations, Cp was shown to increase iron uptake by HepG2 cells, increasing the apparent affinity...
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Veröffentlicht in: | Science (American Association for the Advancement of Science) 1998-01, Vol.279 (5351), p.714-717 |
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description | Individuals with hereditary ceruloplasmin (Cp) deficiency have profound iron accumulation in most tissues, which suggests that Cp is important for normal release of cellular iron. Here, in contrast to expectations, Cp was shown to increase iron uptake by HepG2 cells, increasing the apparent affinity for the substrate by three times. Consistent with its role in iron uptake, Cp synthesis was regulated by iron supply and was increased four-to fivefold after iron depletion. Unlike other iron controllers that are posttranscriptionally regulated, Cp synthesis was transcriptionally regulated. Thus, iron-deficient cells could increase Cp synthesis to maintain intracellular iron homeostasis, so that defects would lead to global accumulation of iron in tissues. |
doi_str_mv | 10.1126/science.279.5351.714 |
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Here, in contrast to expectations, Cp was shown to increase iron uptake by HepG2 cells, increasing the apparent affinity for the substrate by three times. Consistent with its role in iron uptake, Cp synthesis was regulated by iron supply and was increased four-to fivefold after iron depletion. Unlike other iron controllers that are posttranscriptionally regulated, Cp synthesis was transcriptionally regulated. Thus, iron-deficient cells could increase Cp synthesis to maintain intracellular iron homeostasis, so that defects would lead to global accumulation of iron in tissues.</description><identifier>ISSN: 0036-8075</identifier><identifier>EISSN: 1095-9203</identifier><identifier>DOI: 10.1126/science.279.5351.714</identifier><identifier>PMID: 9445478</identifier><identifier>CODEN: SCIEAS</identifier><language>eng</language><publisher>Washington, DC: American Society for the Advancement of Science</publisher><subject>Antibodies ; Biological and medical sciences ; Biological Transport ; Cell metabolism ; Cell physiology ; Cellular biology ; Ceruloplasmin - biosynthesis ; Ceruloplasmin - genetics ; Ceruloplasmin - pharmacology ; Ceruloplasmin - physiology ; Chlorides ; Complementary DNA ; Culture Media, Conditioned ; Ferric Compounds - pharmacology ; Fundamental and applied biological sciences. Psychology ; Hep G2 cells ; Hepatocytes ; Homeostasis ; Humans ; Iron ; Iron (Nutrient) ; Iron - metabolism ; Iron Chelating Agents - pharmacology ; Iron in the body ; Liver - metabolism ; Membrane and intracellular transports ; Messenger RNA ; Molecular and cellular biology ; Observations ; Oxidases ; Patients ; Physiological aspects ; Physiological regulation ; RNA ; RNA, Messenger - genetics ; RNA, Messenger - metabolism ; Space life sciences ; Transcription, Genetic ; Transferrin - metabolism ; Transferrins ; Tumor Cells, Cultured ; Yeasts</subject><ispartof>Science (American Association for the Advancement of Science), 1998-01, Vol.279 (5351), p.714-717</ispartof><rights>Copyright 1998 American Association for the Advancement of Science</rights><rights>1998 INIST-CNRS</rights><rights>COPYRIGHT 1998 American Association for the Advancement of Science</rights><rights>COPYRIGHT 1998 American Association for the Advancement of Science</rights><rights>Copyright American Association for the Advancement of Science Jan 30, 1998</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c782t-193d061a7c3093892ebcaf2b878183fc8d63f8c1821e8bc6450a3afab83b9eed3</citedby><cites>FETCH-LOGICAL-c782t-193d061a7c3093892ebcaf2b878183fc8d63f8c1821e8bc6450a3afab83b9eed3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/2894295$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/2894295$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,780,784,803,2884,2885,27924,27925,58017,58250</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2140322$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9445478$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Mukhopadhyay, Chinmay K.</creatorcontrib><creatorcontrib>Attieh, Zouhair K.</creatorcontrib><creatorcontrib>Fox, Paul L.</creatorcontrib><title>Role of Ceruloplasmin in Cellular Iron Uptake</title><title>Science (American Association for the Advancement of Science)</title><addtitle>Science</addtitle><description>Individuals with hereditary ceruloplasmin (Cp) deficiency have profound iron accumulation in most tissues, which suggests that Cp is important for normal release of cellular iron. Here, in contrast to expectations, Cp was shown to increase iron uptake by HepG2 cells, increasing the apparent affinity for the substrate by three times. Consistent with its role in iron uptake, Cp synthesis was regulated by iron supply and was increased four-to fivefold after iron depletion. Unlike other iron controllers that are posttranscriptionally regulated, Cp synthesis was transcriptionally regulated. Thus, iron-deficient cells could increase Cp synthesis to maintain intracellular iron homeostasis, so that defects would lead to global accumulation of iron in tissues.</description><subject>Antibodies</subject><subject>Biological and medical sciences</subject><subject>Biological Transport</subject><subject>Cell metabolism</subject><subject>Cell physiology</subject><subject>Cellular biology</subject><subject>Ceruloplasmin - biosynthesis</subject><subject>Ceruloplasmin - genetics</subject><subject>Ceruloplasmin - pharmacology</subject><subject>Ceruloplasmin - physiology</subject><subject>Chlorides</subject><subject>Complementary DNA</subject><subject>Culture Media, Conditioned</subject><subject>Ferric Compounds - pharmacology</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Hep G2 cells</subject><subject>Hepatocytes</subject><subject>Homeostasis</subject><subject>Humans</subject><subject>Iron</subject><subject>Iron (Nutrient)</subject><subject>Iron - metabolism</subject><subject>Iron Chelating Agents - pharmacology</subject><subject>Iron in the body</subject><subject>Liver - metabolism</subject><subject>Membrane and intracellular transports</subject><subject>Messenger RNA</subject><subject>Molecular and cellular biology</subject><subject>Observations</subject><subject>Oxidases</subject><subject>Patients</subject><subject>Physiological aspects</subject><subject>Physiological regulation</subject><subject>RNA</subject><subject>RNA, Messenger - genetics</subject><subject>RNA, Messenger - metabolism</subject><subject>Space life sciences</subject><subject>Transcription, Genetic</subject><subject>Transferrin - metabolism</subject><subject>Transferrins</subject><subject>Tumor Cells, Cultured</subject><subject>Yeasts</subject><issn>0036-8075</issn><issn>1095-9203</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqN0m2r0zAUB_AgynVOv8EVioj64nbmoW2Sl9eiczAcqNe3IU1PR2fazKQF_fZmrFyZDB0tFHJ-55By_ghdE7wghBZvg2mhN7CgXC5ylpMFJ9kDNCNY5qmkmD1EM4xZkQrM88foSQg7jGNNsit0JbMsz7iYofSzs5C4JinBj9btrQ5d2yfxLcHa0WqfrLzrk7v9oL_DU_So0TbAs-k7R3cf3n8tP6brzXJV3q5TwwUdUiJZjQuiuWFYMiEpVEY3tBJcEMEaI-qCNcIQQQmIyhRZjjXTja4EqyRAzebo1XHu3rsfI4RBdW0w8UK6BzcGxWVRCMFkhK__DTPGGccC_3ckKRjhFB9GvvgL7tzo-_i7ihKWc04pi-jmiLbagmr7xg1emy304LV1PTRtPL6NSyjyODLy9AyPTw1da875Nyc-kgF-Dls9hqBWXz5dTDffLqbvlpdSsVyf0Jtz1DhrYQsq5qLcnPDsyI13IXho1N63nfa_FMHqkGs15VrFXKtDrlXMdWx7Pm1lrDqo75umIMf6y6mug9G28bo3bbhnlGSYxcXN0fWR7cLg_J-ykBmVOfsNkkYDkQ</recordid><startdate>19980130</startdate><enddate>19980130</enddate><creator>Mukhopadhyay, Chinmay K.</creator><creator>Attieh, Zouhair K.</creator><creator>Fox, Paul L.</creator><general>American Society for the Advancement of Science</general><general>American Association for the Advancement of Science</general><general>The American Association for the Advancement of Science</general><scope>IQODW</scope><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>8GL</scope><scope>IBG</scope><scope>IOV</scope><scope>ISN</scope><scope>0-V</scope><scope>3V.</scope><scope>7QF</scope><scope>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QQ</scope><scope>7QR</scope><scope>7SC</scope><scope>7SE</scope><scope>7SN</scope><scope>7SP</scope><scope>7SR</scope><scope>7SS</scope><scope>7T7</scope><scope>7TA</scope><scope>7TB</scope><scope>7TK</scope><scope>7TM</scope><scope>7U5</scope><scope>7U9</scope><scope>7X2</scope><scope>7X7</scope><scope>7XB</scope><scope>88A</scope><scope>88B</scope><scope>88E</scope><scope>88I</scope><scope>8AF</scope><scope>8BQ</scope><scope>8FD</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABJCF</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ALSLI</scope><scope>ARAPS</scope><scope>ATCPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BEC</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>BKSAR</scope><scope>C1K</scope><scope>CCPQU</scope><scope>CJNVE</scope><scope>D1I</scope><scope>DWQXO</scope><scope>F28</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>H8D</scope><scope>H8G</scope><scope>H94</scope><scope>HCIFZ</scope><scope>JG9</scope><scope>JQ2</scope><scope>K9-</scope><scope>K9.</scope><scope>KB.</scope><scope>KR7</scope><scope>L6V</scope><scope>L7M</scope><scope>LK8</scope><scope>L~C</scope><scope>L~D</scope><scope>M0K</scope><scope>M0P</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>M2O</scope><scope>M2P</scope><scope>M7N</scope><scope>M7P</scope><scope>M7S</scope><scope>MBDVC</scope><scope>P5Z</scope><scope>P62</scope><scope>P64</scope><scope>PATMY</scope><scope>PCBAR</scope><scope>PDBOC</scope><scope>PQEDU</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PTHSS</scope><scope>PYCSY</scope><scope>Q9U</scope><scope>R05</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>19980130</creationdate><title>Role of Ceruloplasmin in Cellular Iron Uptake</title><author>Mukhopadhyay, Chinmay K. ; Attieh, Zouhair K. ; Fox, Paul L.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c782t-193d061a7c3093892ebcaf2b878183fc8d63f8c1821e8bc6450a3afab83b9eed3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Antibodies</topic><topic>Biological and medical sciences</topic><topic>Biological Transport</topic><topic>Cell metabolism</topic><topic>Cell physiology</topic><topic>Cellular biology</topic><topic>Ceruloplasmin - biosynthesis</topic><topic>Ceruloplasmin - genetics</topic><topic>Ceruloplasmin - pharmacology</topic><topic>Ceruloplasmin - physiology</topic><topic>Chlorides</topic><topic>Complementary DNA</topic><topic>Culture Media, Conditioned</topic><topic>Ferric Compounds - pharmacology</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Hep G2 cells</topic><topic>Hepatocytes</topic><topic>Homeostasis</topic><topic>Humans</topic><topic>Iron</topic><topic>Iron (Nutrient)</topic><topic>Iron - metabolism</topic><topic>Iron Chelating Agents - pharmacology</topic><topic>Iron in the body</topic><topic>Liver - metabolism</topic><topic>Membrane and intracellular transports</topic><topic>Messenger RNA</topic><topic>Molecular and cellular biology</topic><topic>Observations</topic><topic>Oxidases</topic><topic>Patients</topic><topic>Physiological aspects</topic><topic>Physiological regulation</topic><topic>RNA</topic><topic>RNA, Messenger - genetics</topic><topic>RNA, Messenger - metabolism</topic><topic>Space life sciences</topic><topic>Transcription, Genetic</topic><topic>Transferrin - metabolism</topic><topic>Transferrins</topic><topic>Tumor Cells, Cultured</topic><topic>Yeasts</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Mukhopadhyay, Chinmay 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Here, in contrast to expectations, Cp was shown to increase iron uptake by HepG2 cells, increasing the apparent affinity for the substrate by three times. Consistent with its role in iron uptake, Cp synthesis was regulated by iron supply and was increased four-to fivefold after iron depletion. Unlike other iron controllers that are posttranscriptionally regulated, Cp synthesis was transcriptionally regulated. Thus, iron-deficient cells could increase Cp synthesis to maintain intracellular iron homeostasis, so that defects would lead to global accumulation of iron in tissues.</abstract><cop>Washington, DC</cop><pub>American Society for the Advancement of Science</pub><pmid>9445478</pmid><doi>10.1126/science.279.5351.714</doi><tpages>4</tpages></addata></record> |
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subjects | Antibodies Biological and medical sciences Biological Transport Cell metabolism Cell physiology Cellular biology Ceruloplasmin - biosynthesis Ceruloplasmin - genetics Ceruloplasmin - pharmacology Ceruloplasmin - physiology Chlorides Complementary DNA Culture Media, Conditioned Ferric Compounds - pharmacology Fundamental and applied biological sciences. Psychology Hep G2 cells Hepatocytes Homeostasis Humans Iron Iron (Nutrient) Iron - metabolism Iron Chelating Agents - pharmacology Iron in the body Liver - metabolism Membrane and intracellular transports Messenger RNA Molecular and cellular biology Observations Oxidases Patients Physiological aspects Physiological regulation RNA RNA, Messenger - genetics RNA, Messenger - metabolism Space life sciences Transcription, Genetic Transferrin - metabolism Transferrins Tumor Cells, Cultured Yeasts |
title | Role of Ceruloplasmin in Cellular Iron Uptake |
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