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Role of Iron Chelators in Growth-Promoting Effect on Mouse Hybridoma Cells in a Chemically Defined Medium
The role of various iron chelators on the multiplication of mouse hybridoma cells in an albumin-free, transferrin-deficient defined medium was investigated. Fe(III)-dihydroxyethylglycine, Fe(III)-glycylglycine, Fe(III)-ethylenediamine-N,N'-dipropionic acid, or Fe(III)-iminodiacetic acid support...
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Published in: | In Vitro Cellular & Developmental Biology 1987-12, Vol.23 (12), p.815-820 |
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container_title | In Vitro Cellular & Developmental Biology |
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creator | Noritsugu Yabe Miwa Kato Matsuya, Yutaka Isao Yamane Muneaki Iizuka Hiroyuki Takayoshi Kiyokazu Suzuki |
description | The role of various iron chelators on the multiplication of mouse hybridoma cells in an albumin-free, transferrin-deficient defined medium was investigated. Fe(III)-dihydroxyethylglycine, Fe(III)-glycylglycine, Fe(III)-ethylenediamine-N,N'-dipropionic acid, or Fe(III)-iminodiacetic acid supported the excellent growth of the cells. In addition, the growth of the iron-starved cells, which had been preincubated in a protein-, iron- and chelator-free defined medium, restored rapidly when the medium was supplemented with holotransferrin, ferric iron, and chelator compared to that when supplemented with holotransferrin, but without iron and chelator. The results suggest that such chelators modulate a progression of transferrin cycle in the presence of transferrin and ferric iron. An alternative explanation is that there is a decrease in generation of iron-catalyzed free radicals. |
doi_str_mv | 10.1007/BF02620959 |
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Fe(III)-dihydroxyethylglycine, Fe(III)-glycylglycine, Fe(III)-ethylenediamine-N,N'-dipropionic acid, or Fe(III)-iminodiacetic acid supported the excellent growth of the cells. In addition, the growth of the iron-starved cells, which had been preincubated in a protein-, iron- and chelator-free defined medium, restored rapidly when the medium was supplemented with holotransferrin, ferric iron, and chelator compared to that when supplemented with holotransferrin, but without iron and chelator. The results suggest that such chelators modulate a progression of transferrin cycle in the presence of transferrin and ferric iron. An alternative explanation is that there is a decrease in generation of iron-catalyzed free radicals.</description><identifier>ISSN: 0883-8364</identifier><identifier>EISSN: 2327-431X</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/BF02620959</identifier><identifier>PMID: 3693250</identifier><identifier>CODEN: ICDBEO</identifier><language>eng</language><publisher>Largo, MD: Tissue Culture Association, Inc</publisher><subject>Animal cells ; Animals ; Biological and medical sciences ; Biotechnology ; Cell culture techniques ; Cell cultures. Hybridization. Fusion ; Cell Division - drug effects ; Cell growth ; Chlorides ; Culture Media - pharmacology ; Cultured cells ; Dose-Response Relationship, Drug ; Establishment of new cell lines, improvement of cultural methods, mass cultures ; Eukaryotic cell cultures ; Ferric Compounds - pharmacology ; Free radicals ; Fundamental and applied biological sciences. Psychology ; Growth Substances - pharmacology ; Hybridomas ; Hybridomas - cytology ; Hybridomas - drug effects ; Imino acids ; Iron ; Iron Chelating Agents - pharmacology ; Iron deficiency anemia ; Methods. Procedures. Technologies ; Mice ; Mice, Inbred BALB C ; Molecular and cellular biology ; Serum Albumin ; Time Factors ; Transferrin - pharmacology ; Transferrins</subject><ispartof>In Vitro Cellular & Developmental Biology, 1987-12, Vol.23 (12), p.815-820</ispartof><rights>Copyright 1987 Tissue Culture Association</rights><rights>1988 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c332t-98aaafee6de631c7d4830fb818f49cd3005db022706f654e3152441e0c64e4523</citedby><cites>FETCH-LOGICAL-c332t-98aaafee6de631c7d4830fb818f49cd3005db022706f654e3152441e0c64e4523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/4296157$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/4296157$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>314,776,780,27901,27902,58213,58446</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=7724880$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/3693250$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Noritsugu Yabe</creatorcontrib><creatorcontrib>Miwa Kato</creatorcontrib><creatorcontrib>Matsuya, Yutaka</creatorcontrib><creatorcontrib>Isao Yamane</creatorcontrib><creatorcontrib>Muneaki Iizuka</creatorcontrib><creatorcontrib>Hiroyuki Takayoshi</creatorcontrib><creatorcontrib>Kiyokazu Suzuki</creatorcontrib><title>Role of Iron Chelators in Growth-Promoting Effect on Mouse Hybridoma Cells in a Chemically Defined Medium</title><title>In Vitro Cellular & Developmental Biology</title><addtitle>In Vitro Cell Dev Biol</addtitle><description>The role of various iron chelators on the multiplication of mouse hybridoma cells in an albumin-free, transferrin-deficient defined medium was investigated. Fe(III)-dihydroxyethylglycine, Fe(III)-glycylglycine, Fe(III)-ethylenediamine-N,N'-dipropionic acid, or Fe(III)-iminodiacetic acid supported the excellent growth of the cells. In addition, the growth of the iron-starved cells, which had been preincubated in a protein-, iron- and chelator-free defined medium, restored rapidly when the medium was supplemented with holotransferrin, ferric iron, and chelator compared to that when supplemented with holotransferrin, but without iron and chelator. The results suggest that such chelators modulate a progression of transferrin cycle in the presence of transferrin and ferric iron. An alternative explanation is that there is a decrease in generation of iron-catalyzed free radicals.</description><subject>Animal cells</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cell culture techniques</subject><subject>Cell cultures. Hybridization. Fusion</subject><subject>Cell Division - drug effects</subject><subject>Cell growth</subject><subject>Chlorides</subject><subject>Culture Media - pharmacology</subject><subject>Cultured cells</subject><subject>Dose-Response Relationship, Drug</subject><subject>Establishment of new cell lines, improvement of cultural methods, mass cultures</subject><subject>Eukaryotic cell cultures</subject><subject>Ferric Compounds - pharmacology</subject><subject>Free radicals</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Growth Substances - pharmacology</subject><subject>Hybridomas</subject><subject>Hybridomas - cytology</subject><subject>Hybridomas - drug effects</subject><subject>Imino acids</subject><subject>Iron</subject><subject>Iron Chelating Agents - pharmacology</subject><subject>Iron deficiency anemia</subject><subject>Methods. Procedures. Technologies</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>Molecular and cellular biology</subject><subject>Serum Albumin</subject><subject>Time Factors</subject><subject>Transferrin - pharmacology</subject><subject>Transferrins</subject><issn>0883-8364</issn><issn>2327-431X</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1987</creationdate><recordtype>article</recordtype><recordid>eNpFkE1PGzEQhi3UKg2UC2cq-YB6qLTt-GNt7xHSBJCIWlVF4rZyvONitLsGeyOUf8-micJpDu8zr2YeQs4YfGcA-sfVArjiUJXVEZlywXUhBXv4QKZgjCiMUPITOc75CUCA4nxCJkJVgpcwJeFPbJFGT29T7OnsEVs7xJRp6Ol1iq_DY_E7xS4Oof9H596jG-jILeM6I73ZrFJoYmfpDNv2_47dVnTB2bbd0J_oQ48NXWIT1t1n8tHbNuPpfp6Q-8X87-ymuPt1fTu7vCucEHwoKmOt9YiqQSWY0400AvzKMONl5RoBUDYr4FyD8qqUKFjJpWQITkmUJRcn5Ouu9znFlzXmoe5CduOBtsfx7Fpro5kAOYLfdqBLMeeEvn5OobNpUzOot17rd68j_GXful512BzQvcgxv9jnNo_f-2R7F_IB05pLY7bY-Q57yqPmQyx5pVipxRvVW4dc</recordid><startdate>19871201</startdate><enddate>19871201</enddate><creator>Noritsugu Yabe</creator><creator>Miwa Kato</creator><creator>Matsuya, Yutaka</creator><creator>Isao Yamane</creator><creator>Muneaki Iizuka</creator><creator>Hiroyuki Takayoshi</creator><creator>Kiyokazu Suzuki</creator><general>Tissue Culture Association, Inc</general><general>Society for In Vitro Biology</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>7X8</scope></search><sort><creationdate>19871201</creationdate><title>Role of Iron Chelators in Growth-Promoting Effect on Mouse Hybridoma Cells in a Chemically Defined Medium</title><author>Noritsugu Yabe ; Miwa Kato ; Matsuya, Yutaka ; Isao Yamane ; Muneaki Iizuka ; Hiroyuki Takayoshi ; Kiyokazu Suzuki</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c332t-98aaafee6de631c7d4830fb818f49cd3005db022706f654e3152441e0c64e4523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1987</creationdate><topic>Animal cells</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Biotechnology</topic><topic>Cell culture techniques</topic><topic>Cell cultures. Hybridization. Fusion</topic><topic>Cell Division - drug effects</topic><topic>Cell growth</topic><topic>Chlorides</topic><topic>Culture Media - pharmacology</topic><topic>Cultured cells</topic><topic>Dose-Response Relationship, Drug</topic><topic>Establishment of new cell lines, improvement of cultural methods, mass cultures</topic><topic>Eukaryotic cell cultures</topic><topic>Ferric Compounds - pharmacology</topic><topic>Free radicals</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Growth Substances - pharmacology</topic><topic>Hybridomas</topic><topic>Hybridomas - cytology</topic><topic>Hybridomas - drug effects</topic><topic>Imino acids</topic><topic>Iron</topic><topic>Iron Chelating Agents - pharmacology</topic><topic>Iron deficiency anemia</topic><topic>Methods. Procedures. Technologies</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>Molecular and cellular biology</topic><topic>Serum Albumin</topic><topic>Time Factors</topic><topic>Transferrin - pharmacology</topic><topic>Transferrins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Noritsugu Yabe</creatorcontrib><creatorcontrib>Miwa Kato</creatorcontrib><creatorcontrib>Matsuya, Yutaka</creatorcontrib><creatorcontrib>Isao Yamane</creatorcontrib><creatorcontrib>Muneaki Iizuka</creatorcontrib><creatorcontrib>Hiroyuki Takayoshi</creatorcontrib><creatorcontrib>Kiyokazu Suzuki</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>In Vitro Cellular & Developmental Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Noritsugu Yabe</au><au>Miwa Kato</au><au>Matsuya, Yutaka</au><au>Isao Yamane</au><au>Muneaki Iizuka</au><au>Hiroyuki Takayoshi</au><au>Kiyokazu Suzuki</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Role of Iron Chelators in Growth-Promoting Effect on Mouse Hybridoma Cells in a Chemically Defined Medium</atitle><jtitle>In Vitro Cellular & Developmental Biology</jtitle><addtitle>In Vitro Cell Dev Biol</addtitle><date>1987-12-01</date><risdate>1987</risdate><volume>23</volume><issue>12</issue><spage>815</spage><epage>820</epage><pages>815-820</pages><issn>0883-8364</issn><eissn>2327-431X</eissn><eissn>1475-2689</eissn><coden>ICDBEO</coden><abstract>The role of various iron chelators on the multiplication of mouse hybridoma cells in an albumin-free, transferrin-deficient defined medium was investigated. Fe(III)-dihydroxyethylglycine, Fe(III)-glycylglycine, Fe(III)-ethylenediamine-N,N'-dipropionic acid, or Fe(III)-iminodiacetic acid supported the excellent growth of the cells. In addition, the growth of the iron-starved cells, which had been preincubated in a protein-, iron- and chelator-free defined medium, restored rapidly when the medium was supplemented with holotransferrin, ferric iron, and chelator compared to that when supplemented with holotransferrin, but without iron and chelator. The results suggest that such chelators modulate a progression of transferrin cycle in the presence of transferrin and ferric iron. An alternative explanation is that there is a decrease in generation of iron-catalyzed free radicals.</abstract><cop>Largo, MD</cop><pub>Tissue Culture Association, Inc</pub><pmid>3693250</pmid><doi>10.1007/BF02620959</doi><tpages>6</tpages></addata></record> |
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subjects | Animal cells Animals Biological and medical sciences Biotechnology Cell culture techniques Cell cultures. Hybridization. Fusion Cell Division - drug effects Cell growth Chlorides Culture Media - pharmacology Cultured cells Dose-Response Relationship, Drug Establishment of new cell lines, improvement of cultural methods, mass cultures Eukaryotic cell cultures Ferric Compounds - pharmacology Free radicals Fundamental and applied biological sciences. Psychology Growth Substances - pharmacology Hybridomas Hybridomas - cytology Hybridomas - drug effects Imino acids Iron Iron Chelating Agents - pharmacology Iron deficiency anemia Methods. Procedures. Technologies Mice Mice, Inbred BALB C Molecular and cellular biology Serum Albumin Time Factors Transferrin - pharmacology Transferrins |
title | Role of Iron Chelators in Growth-Promoting Effect on Mouse Hybridoma Cells in a Chemically Defined Medium |
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