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Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen
The subset of B lymphocytes having IgG on their surfaces was purified from human spleen and blood using a fluorescence-activated cell sorter (FACS). This subset constituted about 15% of B lymphocytes. The remaining non-IgG-bearing B cells were also obtained for study. These two populations were exam...
Formato: | Texto |
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Lenguaje: | English |
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The Rockefeller University Press
1981
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186092/ https://www.ncbi.nlm.nih.gov/pubmed/7017061 |
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collection | PubMed |
description | The subset of B lymphocytes having IgG on their surfaces was purified from human spleen and blood using a fluorescence-activated cell sorter (FACS). This subset constituted about 15% of B lymphocytes. The remaining non-IgG-bearing B cells were also obtained for study. These two populations were examined for (a) their expression of other surface immunoglobulin isotypes, (b) their ability to give rise to IgG- and IgM- secreting (plaque-forming) cells in a pokeweed mitogen (PWM)-driven culture system, and (c) their ability to proliferate in response to PWM stimulation. The results of these studies indicate that most IgG- bearing B cells also express surface IgM and IgD. Less than 15% had only IgG. The IgG-positive cell gave rise to both IgG and IgM plaque- forming cells when driven by PWM, and in fact were responsible for most of the total plaque response in both the IgG and IgM classes. The non- IgG-bearing B cells were depleted of both IgG and IgM responsiveness. The failure of the non-IgG-bearing B cells to give a strong response to PWM did not appear to be due to either depletion of accessory cells or to any suppressive influence. Finally, proliferation studies indicated that both the IgG-bearing and the non-IgG-bearing cells proliferated in the presence of PWM with a somewhat stronger proliferative response in the IgG-bearing cells. These results demonstrate that the IgG-bearing cell is not irreversibly committed to IgG production but can also give rise to IgM-secreting cells, and that human PWM-driven immunoglobulin secretory responses are predominantly due to a numerically small subset of B cells. |
format | Text |
id | pubmed-2186092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1981 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-21860922008-04-17 Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen J Exp Med Articles The subset of B lymphocytes having IgG on their surfaces was purified from human spleen and blood using a fluorescence-activated cell sorter (FACS). This subset constituted about 15% of B lymphocytes. The remaining non-IgG-bearing B cells were also obtained for study. These two populations were examined for (a) their expression of other surface immunoglobulin isotypes, (b) their ability to give rise to IgG- and IgM- secreting (plaque-forming) cells in a pokeweed mitogen (PWM)-driven culture system, and (c) their ability to proliferate in response to PWM stimulation. The results of these studies indicate that most IgG- bearing B cells also express surface IgM and IgD. Less than 15% had only IgG. The IgG-positive cell gave rise to both IgG and IgM plaque- forming cells when driven by PWM, and in fact were responsible for most of the total plaque response in both the IgG and IgM classes. The non- IgG-bearing B cells were depleted of both IgG and IgM responsiveness. The failure of the non-IgG-bearing B cells to give a strong response to PWM did not appear to be due to either depletion of accessory cells or to any suppressive influence. Finally, proliferation studies indicated that both the IgG-bearing and the non-IgG-bearing cells proliferated in the presence of PWM with a somewhat stronger proliferative response in the IgG-bearing cells. These results demonstrate that the IgG-bearing cell is not irreversibly committed to IgG production but can also give rise to IgM-secreting cells, and that human PWM-driven immunoglobulin secretory responses are predominantly due to a numerically small subset of B cells. The Rockefeller University Press 1981-02-01 /pmc/articles/PMC2186092/ /pubmed/7017061 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 Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen |
title | Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen |
title_full | Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen |
title_fullStr | Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen |
title_full_unstemmed | Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen |
title_short | Human B lymphocyte subsets. I. IgG-bearing B cell response to pokeweed mitogen |
title_sort | human b lymphocyte subsets. i. igg-bearing b cell response to pokeweed mitogen |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2186092/ https://www.ncbi.nlm.nih.gov/pubmed/7017061 |