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SDS3 以 AhR 配体特异性的方式与 ARNT 相互作用,调节 CD4+CD8+DPK 胸腺细胞分化中 cKrox 和 S100A4 的表达。

SDS3 interacts with ARNT in an AhR ligand-specific manner regulating expression of cKrox and S100A4 in CD4+CD8+ DPK thymocytes differentiation.

机构信息

Department of Biology, Changwon National University, Changwon, Kyungnam 641-773, South Korea.

出版信息

Environ Toxicol Pharmacol. 2012 Nov;34(3):858-68. doi: 10.1016/j.etap.2012.08.014. Epub 2012 Sep 4.

Abstract

To study mechanisms underlying differential effects of 2,3,7,8-tetrachlorodibenzo-p-dioxin (TCDD) and benzo(a)pyrene (B(a)P) on thymocyte differentiation, we examined effects of AhR ligands on the differentiation of DPK cells, a CD4(+)CD8(+) thymic lymphoma cell line which can differentiate into CD4(+)CD8(-) thymocytes. In contrast to TCDD, which inhibited the differentiation, B(a)P showed little effect. Antigen-mediated up-regulation of S100A4, S100A6, galectin-1, and TRAF5-like protein was remarkably suppressed by TCDD, but slightly by B(a)P. Immunoprecipitation using anti-ARNT Ab revealed that SDS3, a component of the Sin3/HDAC repressor complex, was associated with ARNT only when DPK cells were incubated with TCDD. Expression of cKrox S100A4 was derepressed when SDS3 protein was reduced. These results indicate that although it is generally known that many AhR ligands such as TCDD and B(a)P function mainly by the AhR/ARNT complex, ligand-specific interaction between SDS3 and ARNT exerts differential effects on the expression of genes associated with thymocyte differentiation.

摘要

为了研究 2,3,7,8-四氯二苯并对二恶英(TCDD)和苯并[a]芘(B(a)P)对胸腺细胞分化的差异影响的机制,我们研究了 AhR 配体对 DPK 细胞分化的影响,DPK 细胞是一种 CD4(+)CD8(+)胸腺淋巴瘤细胞系,可分化为 CD4(+)CD8(-)胸腺细胞。与抑制分化的 TCDD 相反,B(a)P 几乎没有影响。抗原介导的 S100A4、S100A6、半乳糖凝集素-1 和 TRAF5 样蛋白的上调被 TCDD 显著抑制,但被 B(a)P 轻度抑制。使用抗 ARNT Ab 进行免疫沉淀表明,SDS3(Sin3/HDAC 抑制复合物的一个组成部分)仅在 DPK 细胞与 TCDD 孵育时才与 ARNT 相关。当 SDS3 蛋白减少时,cKrox S100A4 的表达被去抑制。这些结果表明,尽管众所周知,许多 AhR 配体,如 TCDD 和 B(a)P,主要通过 AhR/ARNT 复合物发挥作用,但 SDS3 和 ARNT 之间的配体特异性相互作用对与胸腺细胞分化相关的基因的表达产生了不同的影响。

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