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RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS
Guinea pigs immunized with 2,4-dinitrophenyl-guinea pig albumin (DNP-GPA) possess lymphocytes which specifically bind sufficient DNP-GPA-(125)I to their surface to be detected by radioautography. These lymphocytes are present in the draining lymph nodes in a frequency of ∼50/1000 lymphocytes in anim...
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Formato: | Texto |
Lenguaje: | English |
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The Rockefeller University Press
1971
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139043/ https://www.ncbi.nlm.nih.gov/pubmed/5105301 |
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author | Davie, Joseph M. Rosenthal, Alan S. Paul, William E. |
author_facet | Davie, Joseph M. Rosenthal, Alan S. Paul, William E. |
author_sort | Davie, Joseph M. |
collection | PubMed |
description | Guinea pigs immunized with 2,4-dinitrophenyl-guinea pig albumin (DNP-GPA) possess lymphocytes which specifically bind sufficient DNP-GPA-(125)I to their surface to be detected by radioautography. These lymphocytes are present in the draining lymph nodes in a frequency of ∼50/1000 lymphocytes in animals immunized 2–4 wk earlier with DNP-GPA in complete Freund's adjuvant. Nonimmunized animals have ∼0.4 DNP-GPA antigen-binding cells (ABC) per 1000 lymphocytes. An increase in the frequency of DNP-GPA ABC in peripheral blood is detectable by 5 days after immunization, which is before the time that serum anti-DNP antibody is measurable. The receptors of these ABC are hapten specific in that free ε-DNP-L-lysine, at low concentration, inhibits the binding of DNP-GPA-(125)I; DNP bovine serum alumbin (DNP-BSA) is equivalent to DNP-GPA in the inhibition of binding of DNP-GPA-(125)I to ABC; and both DNP-GPA agarose beads and DNP-BSA agarose beads specifically adsorb DNP-GPA-(125)I ABC. Anti-immunoglobulin antisera, particularly anti-γ(2) sera, inhibit the binding of DNP-GPA-(125)I to these cells implying that the receptors are immunoglobulin, primarily of the γ(2) heavy chain class. DNP-GPA-(125)I ABC appear to represent precursors of antibody-secreting cells and have specificity characteristics which are very different from cells, of similarly immunized guinea pigs, which mediate a cellular immune response to DNP-GPA. |
format | Text |
id | pubmed-2139043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1971 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21390432008-04-17 RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS Davie, Joseph M. Rosenthal, Alan S. Paul, William E. J Exp Med Article Guinea pigs immunized with 2,4-dinitrophenyl-guinea pig albumin (DNP-GPA) possess lymphocytes which specifically bind sufficient DNP-GPA-(125)I to their surface to be detected by radioautography. These lymphocytes are present in the draining lymph nodes in a frequency of ∼50/1000 lymphocytes in animals immunized 2–4 wk earlier with DNP-GPA in complete Freund's adjuvant. Nonimmunized animals have ∼0.4 DNP-GPA antigen-binding cells (ABC) per 1000 lymphocytes. An increase in the frequency of DNP-GPA ABC in peripheral blood is detectable by 5 days after immunization, which is before the time that serum anti-DNP antibody is measurable. The receptors of these ABC are hapten specific in that free ε-DNP-L-lysine, at low concentration, inhibits the binding of DNP-GPA-(125)I; DNP bovine serum alumbin (DNP-BSA) is equivalent to DNP-GPA in the inhibition of binding of DNP-GPA-(125)I to ABC; and both DNP-GPA agarose beads and DNP-BSA agarose beads specifically adsorb DNP-GPA-(125)I ABC. Anti-immunoglobulin antisera, particularly anti-γ(2) sera, inhibit the binding of DNP-GPA-(125)I to these cells implying that the receptors are immunoglobulin, primarily of the γ(2) heavy chain class. DNP-GPA-(125)I ABC appear to represent precursors of antibody-secreting cells and have specificity characteristics which are very different from cells, of similarly immunized guinea pigs, which mediate a cellular immune response to DNP-GPA. The Rockefeller University Press 1971-08-01 /pmc/articles/PMC2139043/ /pubmed/5105301 Text en Copyright © 1971 by The Rockefeller University Press This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.rupress.org/terms). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 4.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/4.0/). |
spellingShingle | Article Davie, Joseph M. Rosenthal, Alan S. Paul, William E. RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS |
title | RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS |
title_full | RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS |
title_fullStr | RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS |
title_full_unstemmed | RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS |
title_short | RECEPTORS ON IMMUNOCOMPETENT CELLS : III. SPECIFICITY AND NATURE OF RECEPTORS ON DINITROPHENYLATED GUINEA PIG ALBUMIN-(125)I-BINDING CELLS OF IMMUNIZED GUINEA PIGS |
title_sort | receptors on immunocompetent cells : iii. specificity and nature of receptors on dinitrophenylated guinea pig albumin-(125)i-binding cells of immunized guinea pigs |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2139043/ https://www.ncbi.nlm.nih.gov/pubmed/5105301 |
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