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γ干扰素处理的正常胸腺上皮细胞中CIITA的诱导及体内HLA-DR启动子占据情况的改变:与HLA-DR组成型B细胞的异同

Induction of CIITA and modification of in vivo HLA-DR promoter occupancy in normal thymic epithelial cells treated with IFN-gamma: similarities and distinctions with respect to HLA-DR-constitutive B cells.

作者信息

Rigaud G, De Lerma Barbaro A, Nicolis M, Cestari T, Ramarli D, Riviera A P, Accolla R S

机构信息

Institute of Immunology and Infectious Diseases, School of Medicine, University of Verona, Italy.

出版信息

J Immunol. 1996 Jun 1;156(11):4254-8.

PMID:8666795
Abstract

In this study, the IFN-gamma induction of MHC class II gene expression in primary cultures of thymic epithelial cells (TEC) was analyzed. This cellular system offers the advantage that MHC class II induction is studied in a "physiologic" cell lineage that, as a result of this expression within the thymus, is thought to participate to the selection and maturation of the T cells. It was found that the MHC class II gene expression was associated with the de novo transcription of the gene encoding the CIITA trans-activator, a crucial MHC class II gene regulatory factor. Furthermore, the anatomy of interaction between the MHC class II DRA promoter and corresponding binding factors was analyzed by in vivo DNAse I footprint. It was found that treatment with IFN-gamma induces changes in the occupancy of the DRA gene regulatory sequences by nuclear factors. The resulting occupancy displays strong similarities with the one observed in the MHC class II-constitutive B cells, represented by both the Burkitt lymphoma line Raji and normal tonsil- derived B cells. However, some peculiar differences were observed between the TEC, either IFN-gamma-induced or not, and the constitutive B cells. These results suggest that both common mechanisms, such as the one mediated by the CIITA trans-activator, and distinct tissue-specific constraints contribute to the transcriptional control of constitutive and IFN-gamma-induced MHC class II gene expression.

摘要

在本研究中,分析了胸腺上皮细胞(TEC)原代培养物中MHC II类基因表达的γ干扰素诱导情况。该细胞系统具有这样的优势,即MHC II类诱导是在一种“生理性”细胞谱系中进行研究的,由于这种在胸腺内的表达,该细胞谱系被认为参与T细胞的选择和成熟。研究发现,MHC II类基因表达与编码CIITA反式激活因子的基因的从头转录相关,CIITA是一种关键的MHC II类基因调节因子。此外,通过体内DNA酶I足迹分析了MHC II类DRA启动子与相应结合因子之间的相互作用结构。研究发现,用γ干扰素处理会诱导核因子对DRA基因调控序列的占据发生变化。所产生的占据情况与在MHC II类组成性B细胞中观察到的情况有很强的相似性,MHC II类组成性B细胞以伯基特淋巴瘤细胞系Raji和正常扁桃体来源的B细胞为代表。然而,在TEC(无论是否经γ干扰素诱导)与组成性B细胞之间观察到了一些特殊差异。这些结果表明,诸如由CIITA反式激活因子介导的共同机制以及独特的组织特异性限制因素都对组成性和γ干扰素诱导的MHC II类基因表达的转录控制有贡献。

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