Serum Factors Inhibit Melanoma Cell Surface Expression of Type I and Type II IGF Receptors

Abstract We have identified one class of IGF-I-binding sites and two classes of IGF-II-binding sites at the surface of the melanoma cell line IGR39. By means of affinity labeling with 125I-IGF-I, a 290-300 kDa form was characterized. Using 125I-IGF-II, a 270 kDa polypeptide was labeled, correspondin...

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Veröffentlicht in:Journal of receptors and signal transduction 1996, Vol.16 (1-2), p.115-134
Hauptverfasser: Bellan, C., Remacle-Bonnet, M., Garrouste, F., Secchi, J., Luis, J., Pommier, G., Marvaldi, J.
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container_end_page 134
container_issue 1-2
container_start_page 115
container_title Journal of receptors and signal transduction
container_volume 16
creator Bellan, C.
Remacle-Bonnet, M.
Garrouste, F.
Secchi, J.
Luis, J.
Pommier, G.
Marvaldi, J.
description Abstract We have identified one class of IGF-I-binding sites and two classes of IGF-II-binding sites at the surface of the melanoma cell line IGR39. By means of affinity labeling with 125I-IGF-I, a 290-300 kDa form was characterized. Using 125I-IGF-II, a 270 kDa polypeptide was labeled, corresponding to the type II IGF receptor. In the two serials of experiments, the order of potency in inhibiting 125I-IGF-I or 125I-IGF-II labeling of IGF-related peptides and αIR3, an antibody directed against type I receptor α subunit, was the same as in competition experiments. When IGR39 cells were cultured in a serum-free medium, the number of both high affinity IGF-II and IGF-I binding sites was increased, by 8-and 5-fold respectively, without any significant change in Kd values. In both culture conditions, we found IGFBP-2, -3, -4 and a 30 kDa form which Mr was consistent with IGFBP-5 or -6. Except for IGFBP-2, the amount of secreted IGFBPs was modified depending on culture conditions: in conditioned medium from cells cultured with 10% FCS, the amount of IGFBP-3 or -4 was higher, and the amount of the 30 kDa IGFBP was lower when compared to conditioned medium from cells cultured in serum-free medium.
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By means of affinity labeling with 125I-IGF-I, a 290-300 kDa form was characterized. Using 125I-IGF-II, a 270 kDa polypeptide was labeled, corresponding to the type II IGF receptor. In the two serials of experiments, the order of potency in inhibiting 125I-IGF-I or 125I-IGF-II labeling of IGF-related peptides and αIR3, an antibody directed against type I receptor α subunit, was the same as in competition experiments. When IGR39 cells were cultured in a serum-free medium, the number of both high affinity IGF-II and IGF-I binding sites was increased, by 8-and 5-fold respectively, without any significant change in Kd values. In both culture conditions, we found IGFBP-2, -3, -4 and a 30 kDa form which Mr was consistent with IGFBP-5 or -6. Except for IGFBP-2, the amount of secreted IGFBPs was modified depending on culture conditions: in conditioned medium from cells cultured with 10% FCS, the amount of IGFBP-3 or -4 was higher, and the amount of the 30 kDa IGFBP was lower when compared to conditioned medium from cells cultured in serum-free medium.</description><identifier>ISSN: 1079-9893</identifier><identifier>EISSN: 1532-4281</identifier><identifier>DOI: 10.3109/10799899609039944</identifier><identifier>PMID: 8771534</identifier><language>eng</language><publisher>England: Informa UK Ltd</publisher><subject>Affinity Labels - metabolism ; Binding Sites ; Binding, Competitive ; Blood Proteins - pharmacology ; Blotting, Western ; Cell Line ; Culture Media, Serum-Free ; Gene Expression Regulation, Neoplastic - drug effects ; Humans ; Melanoma - metabolism ; Receptor, IGF Type 1 - biosynthesis ; Receptor, IGF Type 2 - biosynthesis</subject><ispartof>Journal of receptors and signal transduction, 1996, Vol.16 (1-2), p.115-134</ispartof><rights>1996 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 1996</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c401t-9e6d4a84b0d9f04f941cb4ce7e872aba6ed5490eb1738b9388666e32a07c6223</citedby><cites>FETCH-LOGICAL-c401t-9e6d4a84b0d9f04f941cb4ce7e872aba6ed5490eb1738b9388666e32a07c6223</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.3109/10799899609039944$$EPDF$$P50$$Ginformahealthcare$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.3109/10799899609039944$$EHTML$$P50$$Ginformahealthcare$$H</linktohtml><link.rule.ids>314,777,781,4010,27904,27905,27906,59626,59732,60415,60521,61200,61235,61381,61416</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8771534$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Bellan, C.</creatorcontrib><creatorcontrib>Remacle-Bonnet, M.</creatorcontrib><creatorcontrib>Garrouste, F.</creatorcontrib><creatorcontrib>Secchi, J.</creatorcontrib><creatorcontrib>Luis, J.</creatorcontrib><creatorcontrib>Pommier, G.</creatorcontrib><creatorcontrib>Marvaldi, J.</creatorcontrib><title>Serum Factors Inhibit Melanoma Cell Surface Expression of Type I and Type II IGF Receptors</title><title>Journal of receptors and signal transduction</title><addtitle>J Recept Signal Transduct Res</addtitle><description>Abstract We have identified one class of IGF-I-binding sites and two classes of IGF-II-binding sites at the surface of the melanoma cell line IGR39. By means of affinity labeling with 125I-IGF-I, a 290-300 kDa form was characterized. Using 125I-IGF-II, a 270 kDa polypeptide was labeled, corresponding to the type II IGF receptor. In the two serials of experiments, the order of potency in inhibiting 125I-IGF-I or 125I-IGF-II labeling of IGF-related peptides and αIR3, an antibody directed against type I receptor α subunit, was the same as in competition experiments. When IGR39 cells were cultured in a serum-free medium, the number of both high affinity IGF-II and IGF-I binding sites was increased, by 8-and 5-fold respectively, without any significant change in Kd values. In both culture conditions, we found IGFBP-2, -3, -4 and a 30 kDa form which Mr was consistent with IGFBP-5 or -6. Except for IGFBP-2, the amount of secreted IGFBPs was modified depending on culture conditions: in conditioned medium from cells cultured with 10% FCS, the amount of IGFBP-3 or -4 was higher, and the amount of the 30 kDa IGFBP was lower when compared to conditioned medium from cells cultured in serum-free medium.</description><subject>Affinity Labels - metabolism</subject><subject>Binding Sites</subject><subject>Binding, Competitive</subject><subject>Blood Proteins - pharmacology</subject><subject>Blotting, Western</subject><subject>Cell Line</subject><subject>Culture Media, Serum-Free</subject><subject>Gene Expression Regulation, Neoplastic - drug effects</subject><subject>Humans</subject><subject>Melanoma - metabolism</subject><subject>Receptor, IGF Type 1 - biosynthesis</subject><subject>Receptor, IGF Type 2 - biosynthesis</subject><issn>1079-9893</issn><issn>1532-4281</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kEFr3DAUhEVJSNNtf0APAZ1ycytZiiXRXMKymxg2BJo99WKe5WfWi225kk26_75a1gRKaE5vYGY-HkPIV86-Cc7Md86UMdqYjBkmjJHyA7nkNyJNZKr5WdTRT2JAfCSfQtgzxo3i7IJcaKViTl6SX8_op46uwY7OB5r3u6ZsRvqILfSuA7rEtqXPk6_BIl39GTyG0LieuppuDwPSnEJfzTKn-f2a_kSLwxH2mZzX0Ab8Mt8F2a5X2-VDsnm6z5d3m8RKxsfEYFZJ0LJklamZrI3ktpQWFWqVQgkZVjfSMCy5Ero0Qussy1CkwJTN0lQsyPUJO3j3e8IwFl0TbHwbenRTKJROVSbiBgvCT0HrXQge62LwTQf-UHBWHOcs3swZO1czfCo7rF4b837Rvz35TV8738GL821VjHBona899LYJR_T_8T_-qe8Q2nFnwWOxd5Pv42zvPPcX8uOUIQ</recordid><startdate>1996</startdate><enddate>1996</enddate><creator>Bellan, C.</creator><creator>Remacle-Bonnet, M.</creator><creator>Garrouste, F.</creator><creator>Secchi, J.</creator><creator>Luis, J.</creator><creator>Pommier, G.</creator><creator>Marvaldi, J.</creator><general>Informa UK Ltd</general><general>Taylor &amp; Francis</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>7X8</scope></search><sort><creationdate>1996</creationdate><title>Serum Factors Inhibit Melanoma Cell Surface Expression of Type I and Type II IGF Receptors</title><author>Bellan, C. ; Remacle-Bonnet, M. ; Garrouste, F. ; Secchi, J. ; Luis, J. ; Pommier, G. ; Marvaldi, J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c401t-9e6d4a84b0d9f04f941cb4ce7e872aba6ed5490eb1738b9388666e32a07c6223</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Affinity Labels - metabolism</topic><topic>Binding Sites</topic><topic>Binding, Competitive</topic><topic>Blood Proteins - pharmacology</topic><topic>Blotting, Western</topic><topic>Cell Line</topic><topic>Culture Media, Serum-Free</topic><topic>Gene Expression Regulation, Neoplastic - drug effects</topic><topic>Humans</topic><topic>Melanoma - metabolism</topic><topic>Receptor, IGF Type 1 - biosynthesis</topic><topic>Receptor, IGF Type 2 - biosynthesis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Bellan, C.</creatorcontrib><creatorcontrib>Remacle-Bonnet, M.</creatorcontrib><creatorcontrib>Garrouste, F.</creatorcontrib><creatorcontrib>Secchi, J.</creatorcontrib><creatorcontrib>Luis, J.</creatorcontrib><creatorcontrib>Pommier, G.</creatorcontrib><creatorcontrib>Marvaldi, J.</creatorcontrib><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>Journal of receptors and signal transduction</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Bellan, C.</au><au>Remacle-Bonnet, M.</au><au>Garrouste, F.</au><au>Secchi, J.</au><au>Luis, J.</au><au>Pommier, G.</au><au>Marvaldi, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum Factors Inhibit Melanoma Cell Surface Expression of Type I and Type II IGF Receptors</atitle><jtitle>Journal of receptors and signal transduction</jtitle><addtitle>J Recept Signal Transduct Res</addtitle><date>1996</date><risdate>1996</risdate><volume>16</volume><issue>1-2</issue><spage>115</spage><epage>134</epage><pages>115-134</pages><issn>1079-9893</issn><eissn>1532-4281</eissn><abstract>Abstract We have identified one class of IGF-I-binding sites and two classes of IGF-II-binding sites at the surface of the melanoma cell line IGR39. By means of affinity labeling with 125I-IGF-I, a 290-300 kDa form was characterized. Using 125I-IGF-II, a 270 kDa polypeptide was labeled, corresponding to the type II IGF receptor. In the two serials of experiments, the order of potency in inhibiting 125I-IGF-I or 125I-IGF-II labeling of IGF-related peptides and αIR3, an antibody directed against type I receptor α subunit, was the same as in competition experiments. When IGR39 cells were cultured in a serum-free medium, the number of both high affinity IGF-II and IGF-I binding sites was increased, by 8-and 5-fold respectively, without any significant change in Kd values. In both culture conditions, we found IGFBP-2, -3, -4 and a 30 kDa form which Mr was consistent with IGFBP-5 or -6. Except for IGFBP-2, the amount of secreted IGFBPs was modified depending on culture conditions: in conditioned medium from cells cultured with 10% FCS, the amount of IGFBP-3 or -4 was higher, and the amount of the 30 kDa IGFBP was lower when compared to conditioned medium from cells cultured in serum-free medium.</abstract><cop>England</cop><pub>Informa UK Ltd</pub><pmid>8771534</pmid><doi>10.3109/10799899609039944</doi><tpages>20</tpages></addata></record>
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source MEDLINE; Taylor & Francis Medical Library - CRKN; Taylor & Francis Journals Complete
subjects Affinity Labels - metabolism
Binding Sites
Binding, Competitive
Blood Proteins - pharmacology
Blotting, Western
Cell Line
Culture Media, Serum-Free
Gene Expression Regulation, Neoplastic - drug effects
Humans
Melanoma - metabolism
Receptor, IGF Type 1 - biosynthesis
Receptor, IGF Type 2 - biosynthesis
title Serum Factors Inhibit Melanoma Cell Surface Expression of Type I and Type II IGF Receptors
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