Species Specificity of Iron Delivery in Hybridomas

Studies with Human x Human (HxH), Human x Mouse (HxM), and Mouse x Mouse (MxM) hybridomas have enabled us to define specific factors that affect hybridoma growth in a species-specific manner. Three transferons and three lipophilic iron chelates have been tested for their ability to support hybridoma...

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Veröffentlicht in:In Vitro Cellular & Developmental Biology 1988-05, Vol.24 (5), p.413-419
Hauptverfasser: Ill, Charles R., Tammy Brehm, Bjorn K. Lydersen, Rachel Hernandez, Burnett, Karen G.
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container_end_page 419
container_issue 5
container_start_page 413
container_title In Vitro Cellular & Developmental Biology
container_volume 24
creator Ill, Charles R.
Tammy Brehm
Bjorn K. Lydersen
Rachel Hernandez
Burnett, Karen G.
description Studies with Human x Human (HxH), Human x Mouse (HxM), and Mouse x Mouse (MxM) hybridomas have enabled us to define specific factors that affect hybridoma growth in a species-specific manner. Three transferons and three lipophilic iron chelates have been tested for their ability to support hybridoma proliferation and antibody production. The results of these studies demonstrate that HxH hybridomas do not respond to bovine transferrin$a^\dag$concentrations up to$100 \mu g/ml$and are approximately 100-fold less responsive to mouse transferrin than to human transferrin. HxM and MxM hybridomas respond equally to human or mouse transferrin but are 100-fold less sensitive to bovine transferrin. An antibody to the human transferrin receptor inhibited the growth-promoting activity of human or mouse transferrin on HxH hybridomas but was ineffective on HxM hybridomas. This demonstrated the functionality of the human transferrin receptor in HxH hybridomas and that human, mouse, and bovine transferrin were interacting through the mouse transferrin receptor in HxM hybridomas. HxH and HxM hybridomas respond similarly to three different iron chelates exhibiting 80 to 110% of the growth response to human transferrin. MxM hybridomas fail to respond to the iron chelates at similar concentrations, suggesting that the human genome present in the other hybridoma species confers a unique ability for utilizing iron when delivered in this form.
doi_str_mv 10.1007/BF02628492
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Lydersen ; Rachel Hernandez ; Burnett, Karen G.</creator><creatorcontrib>Ill, Charles R. ; Tammy Brehm ; Bjorn K. Lydersen ; Rachel Hernandez ; Burnett, Karen G.</creatorcontrib><description>Studies with Human x Human (HxH), Human x Mouse (HxM), and Mouse x Mouse (MxM) hybridomas have enabled us to define specific factors that affect hybridoma growth in a species-specific manner. Three transferons and three lipophilic iron chelates have been tested for their ability to support hybridoma proliferation and antibody production. The results of these studies demonstrate that HxH hybridomas do not respond to bovine transferrin$a^\dag$concentrations up to$100 \mu g/ml$and are approximately 100-fold less responsive to mouse transferrin than to human transferrin. HxM and MxM hybridomas respond equally to human or mouse transferrin but are 100-fold less sensitive to bovine transferrin. An antibody to the human transferrin receptor inhibited the growth-promoting activity of human or mouse transferrin on HxH hybridomas but was ineffective on HxM hybridomas. This demonstrated the functionality of the human transferrin receptor in HxH hybridomas and that human, mouse, and bovine transferrin were interacting through the mouse transferrin receptor in HxM hybridomas. HxH and HxM hybridomas respond similarly to three different iron chelates exhibiting 80 to 110% of the growth response to human transferrin. MxM hybridomas fail to respond to the iron chelates at similar concentrations, suggesting that the human genome present in the other hybridoma species confers a unique ability for utilizing iron when delivered in this form.</description><identifier>ISSN: 0883-8364</identifier><identifier>ISSN: 0073-5655</identifier><identifier>EISSN: 2327-431X</identifier><identifier>EISSN: 1475-2689</identifier><identifier>DOI: 10.1007/BF02628492</identifier><identifier>PMID: 3372446</identifier><identifier>CODEN: ICDBEO</identifier><language>eng</language><publisher>Largo, MD: Tissue Culture Association, Inc</publisher><subject>Animal cells ; Animals ; Antibodies ; Biological and medical sciences ; Biotechnology ; Cattle ; Cell cultures. Hybridization. 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Lydersen</creatorcontrib><creatorcontrib>Rachel Hernandez</creatorcontrib><creatorcontrib>Burnett, Karen G.</creatorcontrib><title>Species Specificity of Iron Delivery in Hybridomas</title><title>In Vitro Cellular &amp; Developmental Biology</title><addtitle>In Vitro Cell Dev Biol</addtitle><description>Studies with Human x Human (HxH), Human x Mouse (HxM), and Mouse x Mouse (MxM) hybridomas have enabled us to define specific factors that affect hybridoma growth in a species-specific manner. Three transferons and three lipophilic iron chelates have been tested for their ability to support hybridoma proliferation and antibody production. The results of these studies demonstrate that HxH hybridomas do not respond to bovine transferrin$a^\dag$concentrations up to$100 \mu g/ml$and are approximately 100-fold less responsive to mouse transferrin than to human transferrin. HxM and MxM hybridomas respond equally to human or mouse transferrin but are 100-fold less sensitive to bovine transferrin. An antibody to the human transferrin receptor inhibited the growth-promoting activity of human or mouse transferrin on HxH hybridomas but was ineffective on HxM hybridomas. This demonstrated the functionality of the human transferrin receptor in HxH hybridomas and that human, mouse, and bovine transferrin were interacting through the mouse transferrin receptor in HxM hybridomas. HxH and HxM hybridomas respond similarly to three different iron chelates exhibiting 80 to 110% of the growth response to human transferrin. MxM hybridomas fail to respond to the iron chelates at similar concentrations, suggesting that the human genome present in the other hybridoma species confers a unique ability for utilizing iron when delivered in this form.</description><subject>Animal cells</subject><subject>Animals</subject><subject>Antibodies</subject><subject>Biological and medical sciences</subject><subject>Biotechnology</subject><subject>Cattle</subject><subject>Cell cultures. Hybridization. Fusion</subject><subject>Cell growth</subject><subject>Cell hybridization, cell fusion, hybridomas</subject><subject>Cell Line</subject><subject>Cell lines</subject><subject>Chelates</subject><subject>chelating agents</subject><subject>Citrates</subject><subject>Electrophoresis, Polyacrylamide Gel</subject><subject>Enzyme-Linked Immunosorbent Assay</subject><subject>Eukaryotic cell cultures</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Humans</subject><subject>hybridoma</subject><subject>Hybridomas</subject><subject>Hybridomas - metabolism</subject><subject>iron</subject><subject>Iron - metabolism</subject><subject>Methods. Procedures. Technologies</subject><subject>Mice</subject><subject>Molecular and cellular biology</subject><subject>Receptors, Transferrin - metabolism</subject><subject>Species Specificity</subject><subject>transferrin</subject><subject>Transferrin - pharmacology</subject><subject>Transferrin receptors</subject><subject>Transferrins</subject><subject>Ungulates</subject><issn>0883-8364</issn><issn>0073-5655</issn><issn>2327-431X</issn><issn>1475-2689</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1988</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqF0L1Lw0AYBvBDlFqri7NCBnEQou99X8ZarS0UHFRwC5fLBa7ko96lQv57Uxvq6PK-w_PjGR6ELjHcYwD58DgHIohiCTlCY0KJjBnFn8doDErRWFHBTtFZCGsACoKQERpRKgljYozI28YaZ0P0-wtnXNtFTREtfVNHT7Z039Z3kaujRZd5lzeVDufopNBlsBfDn6CP-fP7bBGvXl-Ws-kqNlTQNtYZ5rk2mksllJFAEgoZcFzYRGSa5xnkxNoEJyKHXOlMaoY1t4Xl_RGa0Qm63fdufPO1taFNKxeMLUtd22YbUqkIwyCSfyHmAIwI2sO7PTS-CcHbIt14V2nfpRjS3ZLp35I9vh5at1ll8wMdpuvzmyHXweiy8Lo2LhyYBIk53rGrPVuHtvGHmJFEkH6nH2o2gow</recordid><startdate>19880501</startdate><enddate>19880501</enddate><creator>Ill, Charles R.</creator><creator>Tammy Brehm</creator><creator>Bjorn K. 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Psychology</topic><topic>Humans</topic><topic>hybridoma</topic><topic>Hybridomas</topic><topic>Hybridomas - metabolism</topic><topic>iron</topic><topic>Iron - metabolism</topic><topic>Methods. Procedures. Technologies</topic><topic>Mice</topic><topic>Molecular and cellular biology</topic><topic>Receptors, Transferrin - metabolism</topic><topic>Species Specificity</topic><topic>transferrin</topic><topic>Transferrin - pharmacology</topic><topic>Transferrin receptors</topic><topic>Transferrins</topic><topic>Ungulates</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ill, Charles R.</creatorcontrib><creatorcontrib>Tammy Brehm</creatorcontrib><creatorcontrib>Bjorn K. Lydersen</creatorcontrib><creatorcontrib>Rachel Hernandez</creatorcontrib><creatorcontrib>Burnett, Karen G.</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>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>In Vitro Cellular &amp; Developmental Biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ill, Charles R.</au><au>Tammy Brehm</au><au>Bjorn K. Lydersen</au><au>Rachel Hernandez</au><au>Burnett, Karen G.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Species Specificity of Iron Delivery in Hybridomas</atitle><jtitle>In Vitro Cellular &amp; Developmental Biology</jtitle><addtitle>In Vitro Cell Dev Biol</addtitle><date>1988-05-01</date><risdate>1988</risdate><volume>24</volume><issue>5</issue><spage>413</spage><epage>419</epage><pages>413-419</pages><issn>0883-8364</issn><issn>0073-5655</issn><eissn>2327-431X</eissn><eissn>1475-2689</eissn><coden>ICDBEO</coden><abstract>Studies with Human x Human (HxH), Human x Mouse (HxM), and Mouse x Mouse (MxM) hybridomas have enabled us to define specific factors that affect hybridoma growth in a species-specific manner. Three transferons and three lipophilic iron chelates have been tested for their ability to support hybridoma proliferation and antibody production. The results of these studies demonstrate that HxH hybridomas do not respond to bovine transferrin$a^\dag$concentrations up to$100 \mu g/ml$and are approximately 100-fold less responsive to mouse transferrin than to human transferrin. HxM and MxM hybridomas respond equally to human or mouse transferrin but are 100-fold less sensitive to bovine transferrin. An antibody to the human transferrin receptor inhibited the growth-promoting activity of human or mouse transferrin on HxH hybridomas but was ineffective on HxM hybridomas. This demonstrated the functionality of the human transferrin receptor in HxH hybridomas and that human, mouse, and bovine transferrin were interacting through the mouse transferrin receptor in HxM hybridomas. HxH and HxM hybridomas respond similarly to three different iron chelates exhibiting 80 to 110% of the growth response to human transferrin. MxM hybridomas fail to respond to the iron chelates at similar concentrations, suggesting that the human genome present in the other hybridoma species confers a unique ability for utilizing iron when delivered in this form.</abstract><cop>Largo, MD</cop><pub>Tissue Culture Association, Inc</pub><pmid>3372446</pmid><doi>10.1007/BF02628492</doi><tpages>7</tpages></addata></record>
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identifier ISSN: 0883-8364
ispartof In Vitro Cellular & Developmental Biology, 1988-05, Vol.24 (5), p.413-419
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2327-431X
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source MEDLINE; JSTOR Archive Collection A-Z Listing; SpringerLink Journals - AutoHoldings
subjects Animal cells
Animals
Antibodies
Biological and medical sciences
Biotechnology
Cattle
Cell cultures. Hybridization. Fusion
Cell growth
Cell hybridization, cell fusion, hybridomas
Cell Line
Cell lines
Chelates
chelating agents
Citrates
Electrophoresis, Polyacrylamide Gel
Enzyme-Linked Immunosorbent Assay
Eukaryotic cell cultures
Fundamental and applied biological sciences. Psychology
Humans
hybridoma
Hybridomas
Hybridomas - metabolism
iron
Iron - metabolism
Methods. Procedures. Technologies
Mice
Molecular and cellular biology
Receptors, Transferrin - metabolism
Species Specificity
transferrin
Transferrin - pharmacology
Transferrin receptors
Transferrins
Ungulates
title Species Specificity of Iron Delivery in Hybridomas
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