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细粒棘球蚴感染中阻断TGF-β1受体对淋巴细胞的影响

印双红 杨文才 张俊波 陈小林 徐芳洁 侯隽 吴向未 陈雪玲 姚元勇 邢明明

中国免疫学杂志Issue(5):607-612,6.
中国免疫学杂志Issue(5):607-612,6.DOI:10.3969/j.issn.1000-484X.2015.05.007

细粒棘球蚴感染中阻断TGF-β1受体对淋巴细胞的影响

Effect of inhibition of TGF-β1 receptors on lymphocytes during infection of Echi-nococcus granulosus

印双红 1杨文才 2张俊波 1陈小林 3徐芳洁 3侯隽 3吴向未 3陈雪玲 3姚元勇 1邢明明1

作者信息

  • 1. 铜仁学院材料与化学工程学院,铜仁 554300
  • 2. 铜仁市人民医院检验科,铜仁 554300
  • 3. 石河子大学医学院,石河子 832000
  • 折叠

摘要

Abstract

Objective:To investigate the effects of TGF-β1 on T lymphocytes of BALB/c mice infected with Echinococcus granulosus( E.granulosus ) in vitro.Methods: The inhibitor group:the spleen cells of BALB/c mouse were co-cultured with E.granulosus and SB525334.The control group:the spleen cells of BALB/c mouse were co-cultured with E.granulosus and PBS.The blank group:the spleen cells of BALB/c mouse were co-cultured with RPMI-1640 medium and SB525334.The lymphocytes were collected at 48 h post-infection.The T lymphocyte subsets, the number of CD4+CD25+T cells, the number of NK cells, and the expression of NKG2D receptor were detected by flow cytometry.The NK cell activity was determined with the lactate dehydrogenase leakage assay(LDH).Results:The inhibition the TGF-β1 receptors resulted in the increase of in the number of CD4+T cells,the decrease in the number of CD8+T cells,the increase of in the ratio CD4+/CD8+T cells,the decrease of in the number of CD4+CD25+T cells,the increase in the expression of the NKG2D receptors,the increase in the lysis rate of Yac-1 cells by NK cells,and a positive cor-relation between the expression of activity receptor NKG2D and killing activity of NK, which were mediated by E.granulosus.Conclusion: The inhibition of TGF-β1 receptors can enhance the immune response of T lymphocytes against E.granulosus infection in vitro.

关键词

细粒棘球蚴/T细胞亚群/Treg细胞/NKG2D

Key words

Echinococcus granulosus/T-lymphocyte subsets/Treg cells/NKG2D

分类

医药卫生

引用本文复制引用

印双红,杨文才,张俊波,陈小林,徐芳洁,侯隽,吴向未,陈雪玲,姚元勇,邢明明..细粒棘球蚴感染中阻断TGF-β1受体对淋巴细胞的影响[J].中国免疫学杂志,2015,(5):607-612,6.

基金项目

本文受国家自然科学基金(81260412,81360453)、博士基金(2012BB018,trxyDH1504)及教合KY字[2011]005号资助。 ()

中国免疫学杂志

OA北大核心CSCDCSTPCD

1000-484X

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