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Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response

Spleen cell cultures from young adult mice of a variety of strains were stimulated to incorporate tritiated thymidine ([3H]TdR) by a goat anti- mouse IgM antiserum and by purified anti-mu antibodies prepared from this serum. This stimulation was shown to depend upon the anti-mu activity of the antis...

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Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 1978
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184205/
https://www.ncbi.nlm.nih.gov/pubmed/416168
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description Spleen cell cultures from young adult mice of a variety of strains were stimulated to incorporate tritiated thymidine ([3H]TdR) by a goat anti- mouse IgM antiserum and by purified anti-mu antibodies prepared from this serum. This stimulation was shown to depend upon the anti-mu activity of the antiserum. In addition, ultracentrifuged anti-mu and F(ab')2 fragments of anti-mu were shown to be stimulatory. The anti-mu preparation lacked detectable endotoxin contamination and was also shown to stimulate response by two strains (C57BL/10ScCr and C3H/HeJ) which are unresponsive to the mitogenic effects of endotoxin, while it failed to stimulate a response by cells from a mouse strain (CBA/N) which responds to endotoxin. In addition purified goat anti-mouse gamma, kappa antibodies and rabbit anti-mouse kappa-antib odies stimulated uptake of [3H]TdR by mouse spleen cells, although to a lesser degree than the anti-mu preparation. The cell density, culture requirements, and kinetics of the response are presented.
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spelling pubmed-21842052008-04-17 Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response J Exp Med Articles Spleen cell cultures from young adult mice of a variety of strains were stimulated to incorporate tritiated thymidine ([3H]TdR) by a goat anti- mouse IgM antiserum and by purified anti-mu antibodies prepared from this serum. This stimulation was shown to depend upon the anti-mu activity of the antiserum. In addition, ultracentrifuged anti-mu and F(ab')2 fragments of anti-mu were shown to be stimulatory. The anti-mu preparation lacked detectable endotoxin contamination and was also shown to stimulate response by two strains (C57BL/10ScCr and C3H/HeJ) which are unresponsive to the mitogenic effects of endotoxin, while it failed to stimulate a response by cells from a mouse strain (CBA/N) which responds to endotoxin. In addition purified goat anti-mouse gamma, kappa antibodies and rabbit anti-mouse kappa-antib odies stimulated uptake of [3H]TdR by mouse spleen cells, although to a lesser degree than the anti-mu preparation. The cell density, culture requirements, and kinetics of the response are presented. The Rockefeller University Press 1978-03-01 /pmc/articles/PMC2184205/ /pubmed/416168 Text en 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 Articles
Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response
title Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response
title_full Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response
title_fullStr Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response
title_full_unstemmed Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response
title_short Activation of mouse lymphocytes by anti-immunoglobulin. I. Parameters of the proliferative response
title_sort activation of mouse lymphocytes by anti-immunoglobulin. i. parameters of the proliferative response
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2184205/
https://www.ncbi.nlm.nih.gov/pubmed/416168