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Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats

BACKGROUND: Our previous study suggested that SEB exposure in pregnant rats could lead to the change of T cells subpopulation in both peripheral blood and thymus of the offspring rats. However, rarely is known about the influence of SEB exposure in pregnant rats on T cell subpopulation in the spleen...

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Autores principales: Zhou, Ping, Zhang, Xin-sheng, Xu, Zhi-ben, Gao, Shu-xian, Zheng, Qing-wei, Xu, Ming-zhu, Shen, Lin, Yu, Feng, Guan, Jun-chang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210265/
https://www.ncbi.nlm.nih.gov/pubmed/28049431
http://dx.doi.org/10.1186/s12866-016-0921-2
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author Zhou, Ping
Zhang, Xin-sheng
Xu, Zhi-ben
Gao, Shu-xian
Zheng, Qing-wei
Xu, Ming-zhu
Shen, Lin
Yu, Feng
Guan, Jun-chang
author_facet Zhou, Ping
Zhang, Xin-sheng
Xu, Zhi-ben
Gao, Shu-xian
Zheng, Qing-wei
Xu, Ming-zhu
Shen, Lin
Yu, Feng
Guan, Jun-chang
author_sort Zhou, Ping
collection PubMed
description BACKGROUND: Our previous study suggested that SEB exposure in pregnant rats could lead to the change of T cells subpopulation in both peripheral blood and thymus of the offspring rats. However, rarely is known about the influence of SEB exposure in pregnant rats on T cell subpopulation in the spleens of offspring rats. RESULTS: SEB was intravenously administered to the pregnant rats at gestational day 16 in this study. The percentages, in vivo and in vitro responses of CD4 and CD8 T cells were investigated with flow cytometry. The prenatal SEB exposure obviously increased splenic CD4 T cell percentages of both neonates and adult offspring rats, and obviously reduced splenic CD8 T cell percentages of both the fifth day neonates and adult offspring rats. After spleens in the adult offspring rats were re-stimulated with SEB in vivo or in vitro, in vivo SEB stimulation could lead to the marked decrease of splenic CD4 T cell percentage and the marked increase of splenic CD8 T cell percentage. While in vitro SEB stimulation to the cultured splenocytes markedly decreased the proliferation of the splenic lymphocytes and the CD4 T cell percentage, and had no influence on CD8 T cell percentage. CONCLUSION: The prenatal SEB exposure could alter the percentages of CD4/CD8 T cell subpopulation and the response of CD4 and CD8 T cells to the in vivo and in vitro secondary SEB stimulation in the splenocytes of adult offspring rats.
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spelling pubmed-52102652017-01-06 Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats Zhou, Ping Zhang, Xin-sheng Xu, Zhi-ben Gao, Shu-xian Zheng, Qing-wei Xu, Ming-zhu Shen, Lin Yu, Feng Guan, Jun-chang BMC Microbiol Research Article BACKGROUND: Our previous study suggested that SEB exposure in pregnant rats could lead to the change of T cells subpopulation in both peripheral blood and thymus of the offspring rats. However, rarely is known about the influence of SEB exposure in pregnant rats on T cell subpopulation in the spleens of offspring rats. RESULTS: SEB was intravenously administered to the pregnant rats at gestational day 16 in this study. The percentages, in vivo and in vitro responses of CD4 and CD8 T cells were investigated with flow cytometry. The prenatal SEB exposure obviously increased splenic CD4 T cell percentages of both neonates and adult offspring rats, and obviously reduced splenic CD8 T cell percentages of both the fifth day neonates and adult offspring rats. After spleens in the adult offspring rats were re-stimulated with SEB in vivo or in vitro, in vivo SEB stimulation could lead to the marked decrease of splenic CD4 T cell percentage and the marked increase of splenic CD8 T cell percentage. While in vitro SEB stimulation to the cultured splenocytes markedly decreased the proliferation of the splenic lymphocytes and the CD4 T cell percentage, and had no influence on CD8 T cell percentage. CONCLUSION: The prenatal SEB exposure could alter the percentages of CD4/CD8 T cell subpopulation and the response of CD4 and CD8 T cells to the in vivo and in vitro secondary SEB stimulation in the splenocytes of adult offspring rats. BioMed Central 2017-01-03 /pmc/articles/PMC5210265/ /pubmed/28049431 http://dx.doi.org/10.1186/s12866-016-0921-2 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Zhou, Ping
Zhang, Xin-sheng
Xu, Zhi-ben
Gao, Shu-xian
Zheng, Qing-wei
Xu, Ming-zhu
Shen, Lin
Yu, Feng
Guan, Jun-chang
Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats
title Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats
title_full Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats
title_fullStr Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats
title_full_unstemmed Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats
title_short Staphylococcal enterotoxin B administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats
title_sort staphylococcal enterotoxin b administration in pregnant rats alters the splenic lymphocyte response in adult offspring rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5210265/
https://www.ncbi.nlm.nih.gov/pubmed/28049431
http://dx.doi.org/10.1186/s12866-016-0921-2
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