The inhibition of 2,3-dichloro-1-propanol on T cell in vitro and in vivo

被引:4
|
作者
Lu, Jing [1 ,2 ]
Huang, Guoren [1 ]
Zhang, Shuang [1 ]
Song, Bocui [2 ]
Wang, Zhenning [1 ]
Xu, Linli [1 ]
Zhang, Shuonan [1 ]
Guan, Shuang [1 ,3 ]
机构
[1] Jilin Univ, Lab Nutr & Funct Food, Changchun 130062, Jilin, Peoples R China
[2] Jilin Univ, Coll Vet Med, Minist Educ, Key Lab Zoonosis, Changchun 130062, Jilin, Peoples R China
[3] Jilin Univ, Coll Anim Sci, Changchun 130062, Jilin, Peoples R China
关键词
Inhibition; 2,3-DCP; T-cell; DTH; NF-kappa B; NFAT2; DELAYED-TYPE HYPERSENSITIVITY; POTENTIAL IMMUNOTOXICITY; BALB/C MICE; 3-MONOCHLORO-1,2-PROPANEDIOL; DICHLOROPROPANOL; SUPPRESSION; ACTIVATION; SUBSET; TH1;
D O I
10.1016/j.intimp.2013.06.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
2,3-Dichloro-1-propanol (2,3-DCP) is a member of a group of chemicals known as chloropropanols. Currently, immunotoxicity of 2,3-DCP has not been reported. In the present study, we studied its inhibitory effects on T cell both in vivo and in vitro. The results showed that 2,3-DCP markedly inhibited ConA-induced splenocyte proliferation, Th1 and Th2 cytokine production, CD4(+) T cell populations, and the ratio of CD4(+)/CD8(+) T cells and cell cycle arrest in vitro. In addition, 2,3-DCP markedly suppressed DNFB-induced T-cell-mediated delayed-type hypersensitivity (DTH) reaction in mice. Furthermore, Western blot was used to study how 2,3-DCP affects signal transduction mechanisms. The data revealed that 2,3-DCP could down regulate activation of ConA-induced NF-kappa B and NFAT signal transduction pathways. These observations indicated that 2,3-DCP exhibited negative regulatory effects by directly suppressing T-cell-mediated immune responses in vitro and in vivo. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:321 / 328
页数:8
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