Immunoglobulin M receptors on memory cells of immunoglobulin G antibody‐forming cell clones
The memory cells of two antibody‐forming cell clones had receptors of the IgM class, even though the clones had been producing IgG1 or IgG2a anti‐2,4‐dinitrophenyl antibodies for 9–15 months previously (on exposure to antigen). Thus a phenotypic switch in heavy chain constant region evidently occurr...
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Veröffentlicht in: | European journal of immunology 1976-06, Vol.6 (6), p.443-450 |
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creator | Abney, E. R. Keeler, K. D. Parkhouse, R. M. E. Willcox, H. N. A. |
description | The memory cells of two antibody‐forming cell clones had receptors of the IgM class, even though the clones had been producing IgG1 or IgG2a anti‐2,4‐dinitrophenyl antibodies for 9–15 months previously (on exposure to antigen). Thus a phenotypic switch in heavy chain constant region evidently occurred after re‐exposure of these memory cells to antigen.
To show that, we first removed the clonal cells' surface immunoglobulins by “capping” and “stripping”, with class‐ or subclass‐specific antisera. Then, to assay their remaining receptor activity, the cells were incubated with antigen in vitro, washed and transferred (together with carrier‐primed cells) to irradiated recipients, and their antibody responses to this in vitro boost were assayed by isoelectric focusing. Pretreatment with anti‐μ serum, as well as with anti‐Fab(k), prevented the responses of the IgG1 and IgG2a clones to an in vitro boost, while anti‐γ1, and anti‐γ2a antisera had no effect. An anti‐serum to the putative mouse IgD also had no effect. The anti‐μ serum failed to react with the IgG1 and IgG2a clonal serum antibodies in the test tube. Some other contaminating clones were suppressed completely only by the anti‐Fab serum.
This result strongly suggests that switching in class commitment may occur during the differentiation of memory cells to antibody producers, and may therefore be antigen‐dependent. It also implies that some apparently naïve cells with surface IgM may., in reality, be B memory cells. |
doi_str_mv | 10.1002/eji.1830060612 |
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To show that, we first removed the clonal cells' surface immunoglobulins by “capping” and “stripping”, with class‐ or subclass‐specific antisera. Then, to assay their remaining receptor activity, the cells were incubated with antigen in vitro, washed and transferred (together with carrier‐primed cells) to irradiated recipients, and their antibody responses to this in vitro boost were assayed by isoelectric focusing. Pretreatment with anti‐μ serum, as well as with anti‐Fab(k), prevented the responses of the IgG1 and IgG2a clones to an in vitro boost, while anti‐γ1, and anti‐γ2a antisera had no effect. An anti‐serum to the putative mouse IgD also had no effect. The anti‐μ serum failed to react with the IgG1 and IgG2a clonal serum antibodies in the test tube. Some other contaminating clones were suppressed completely only by the anti‐Fab serum.
This result strongly suggests that switching in class commitment may occur during the differentiation of memory cells to antibody producers, and may therefore be antigen‐dependent. It also implies that some apparently naïve cells with surface IgM may., in reality, be B memory cells.</description><identifier>ISSN: 0014-2980</identifier><identifier>EISSN: 1521-4141</identifier><identifier>DOI: 10.1002/eji.1830060612</identifier><identifier>PMID: 825376</identifier><language>eng</language><publisher>Weinheim: WILEY‐VCH Verlag GmbH</publisher><subject>Animals ; Antibody-Producing Cells - immunology ; Antigens ; B-Lymphocytes - immunology ; Binding Sites ; Clone Cells - immunology ; Dinitrobenzenes - immunology ; Female ; Immunoglobulin Allotypes ; Immunoglobulin G - biosynthesis ; Immunoglobulin M ; Immunoglobulin mu-Chains - analysis ; Immunologic Memory ; Mice ; Mice, Inbred CBA ; Receptors, Antigen, B-Cell - metabolism ; Spleen - immunology</subject><ispartof>European journal of immunology, 1976-06, Vol.6 (6), p.443-450</ispartof><rights>Copyright © 1976 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3392-2e604689725ba8e1c643f228d1854b45e6a190a862a3043b1c8fcc8c5a9c7fa03</citedby><cites>FETCH-LOGICAL-c3392-2e604689725ba8e1c643f228d1854b45e6a190a862a3043b1c8fcc8c5a9c7fa03</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Feji.1830060612$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Feji.1830060612$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/825376$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Abney, E. R.</creatorcontrib><creatorcontrib>Keeler, K. D.</creatorcontrib><creatorcontrib>Parkhouse, R. M. E.</creatorcontrib><creatorcontrib>Willcox, H. N. A.</creatorcontrib><title>Immunoglobulin M receptors on memory cells of immunoglobulin G antibody‐forming cell clones</title><title>European journal of immunology</title><addtitle>Eur J Immunol</addtitle><description>The memory cells of two antibody‐forming cell clones had receptors of the IgM class, even though the clones had been producing IgG1 or IgG2a anti‐2,4‐dinitrophenyl antibodies for 9–15 months previously (on exposure to antigen). Thus a phenotypic switch in heavy chain constant region evidently occurred after re‐exposure of these memory cells to antigen.
To show that, we first removed the clonal cells' surface immunoglobulins by “capping” and “stripping”, with class‐ or subclass‐specific antisera. Then, to assay their remaining receptor activity, the cells were incubated with antigen in vitro, washed and transferred (together with carrier‐primed cells) to irradiated recipients, and their antibody responses to this in vitro boost were assayed by isoelectric focusing. Pretreatment with anti‐μ serum, as well as with anti‐Fab(k), prevented the responses of the IgG1 and IgG2a clones to an in vitro boost, while anti‐γ1, and anti‐γ2a antisera had no effect. An anti‐serum to the putative mouse IgD also had no effect. The anti‐μ serum failed to react with the IgG1 and IgG2a clonal serum antibodies in the test tube. Some other contaminating clones were suppressed completely only by the anti‐Fab serum.
This result strongly suggests that switching in class commitment may occur during the differentiation of memory cells to antibody producers, and may therefore be antigen‐dependent. It also implies that some apparently naïve cells with surface IgM may., in reality, be B memory cells.</description><subject>Animals</subject><subject>Antibody-Producing Cells - immunology</subject><subject>Antigens</subject><subject>B-Lymphocytes - immunology</subject><subject>Binding Sites</subject><subject>Clone Cells - immunology</subject><subject>Dinitrobenzenes - immunology</subject><subject>Female</subject><subject>Immunoglobulin Allotypes</subject><subject>Immunoglobulin G - biosynthesis</subject><subject>Immunoglobulin M</subject><subject>Immunoglobulin mu-Chains - analysis</subject><subject>Immunologic Memory</subject><subject>Mice</subject><subject>Mice, Inbred CBA</subject><subject>Receptors, Antigen, B-Cell - metabolism</subject><subject>Spleen - immunology</subject><issn>0014-2980</issn><issn>1521-4141</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1976</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkLtOwzAUhi3ErRRWJgZPbCnHl7jOiKpSiopYYESW4zqVqyQudiOUjUfgGXkSUlpxmZiOjv7v_Dr6EDonMCAA9Mou3YBIBiBAELqHeiSlJOGEk33UAyA8oZmEY3QS4xIAMpFmR-hQ0pQNRQ89T6uqqf2i9HlTuhrf42CNXa19iNjXuLKVDy02tiy7vcDuLz3Bul673M_bj7f3wofK1YsvGJvS1zaeooNCl9Ge7WYfPd2MH0e3yexhMh1dzxLDWEYTagVwIbMhTXMtLTGCs4JSOScy5TlPrdAkAy0F1Qw4y4mRhTHSpDozw0ID66PLbe8q-JfGxrWqXNz8oWvrm6gkE5RQJjpwsAVN8DEGW6hVcJUOrSKgNjpVp1P96OwOLnbNTV7Z-Te-9dfF2TZ-daVt_ylT47vpr-pPuMmCbw</recordid><startdate>197606</startdate><enddate>197606</enddate><creator>Abney, E. R.</creator><creator>Keeler, K. D.</creator><creator>Parkhouse, R. M. E.</creator><creator>Willcox, H. N. A.</creator><general>WILEY‐VCH Verlag GmbH</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>197606</creationdate><title>Immunoglobulin M receptors on memory cells of immunoglobulin G antibody‐forming cell clones</title><author>Abney, E. R. ; Keeler, K. D. ; Parkhouse, R. M. E. ; Willcox, H. N. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3392-2e604689725ba8e1c643f228d1854b45e6a190a862a3043b1c8fcc8c5a9c7fa03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1976</creationdate><topic>Animals</topic><topic>Antibody-Producing Cells - immunology</topic><topic>Antigens</topic><topic>B-Lymphocytes - immunology</topic><topic>Binding Sites</topic><topic>Clone Cells - immunology</topic><topic>Dinitrobenzenes - immunology</topic><topic>Female</topic><topic>Immunoglobulin Allotypes</topic><topic>Immunoglobulin G - biosynthesis</topic><topic>Immunoglobulin M</topic><topic>Immunoglobulin mu-Chains - analysis</topic><topic>Immunologic Memory</topic><topic>Mice</topic><topic>Mice, Inbred CBA</topic><topic>Receptors, Antigen, B-Cell - metabolism</topic><topic>Spleen - immunology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Abney, E. R.</creatorcontrib><creatorcontrib>Keeler, K. D.</creatorcontrib><creatorcontrib>Parkhouse, R. M. E.</creatorcontrib><creatorcontrib>Willcox, H. N. A.</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>European journal of immunology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Abney, E. R.</au><au>Keeler, K. D.</au><au>Parkhouse, R. M. E.</au><au>Willcox, H. N. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Immunoglobulin M receptors on memory cells of immunoglobulin G antibody‐forming cell clones</atitle><jtitle>European journal of immunology</jtitle><addtitle>Eur J Immunol</addtitle><date>1976-06</date><risdate>1976</risdate><volume>6</volume><issue>6</issue><spage>443</spage><epage>450</epage><pages>443-450</pages><issn>0014-2980</issn><eissn>1521-4141</eissn><abstract>The memory cells of two antibody‐forming cell clones had receptors of the IgM class, even though the clones had been producing IgG1 or IgG2a anti‐2,4‐dinitrophenyl antibodies for 9–15 months previously (on exposure to antigen). Thus a phenotypic switch in heavy chain constant region evidently occurred after re‐exposure of these memory cells to antigen.
To show that, we first removed the clonal cells' surface immunoglobulins by “capping” and “stripping”, with class‐ or subclass‐specific antisera. Then, to assay their remaining receptor activity, the cells were incubated with antigen in vitro, washed and transferred (together with carrier‐primed cells) to irradiated recipients, and their antibody responses to this in vitro boost were assayed by isoelectric focusing. Pretreatment with anti‐μ serum, as well as with anti‐Fab(k), prevented the responses of the IgG1 and IgG2a clones to an in vitro boost, while anti‐γ1, and anti‐γ2a antisera had no effect. An anti‐serum to the putative mouse IgD also had no effect. The anti‐μ serum failed to react with the IgG1 and IgG2a clonal serum antibodies in the test tube. Some other contaminating clones were suppressed completely only by the anti‐Fab serum.
This result strongly suggests that switching in class commitment may occur during the differentiation of memory cells to antibody producers, and may therefore be antigen‐dependent. It also implies that some apparently naïve cells with surface IgM may., in reality, be B memory cells.</abstract><cop>Weinheim</cop><pub>WILEY‐VCH Verlag GmbH</pub><pmid>825376</pmid><doi>10.1002/eji.1830060612</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Antibody-Producing Cells - immunology Antigens B-Lymphocytes - immunology Binding Sites Clone Cells - immunology Dinitrobenzenes - immunology Female Immunoglobulin Allotypes Immunoglobulin G - biosynthesis Immunoglobulin M Immunoglobulin mu-Chains - analysis Immunologic Memory Mice Mice, Inbred CBA Receptors, Antigen, B-Cell - metabolism Spleen - immunology |
title | Immunoglobulin M receptors on memory cells of immunoglobulin G antibody‐forming cell clones |
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