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诱导共刺激分子(ICOS)的基因变异调节ICOS的mRNA水平以及细胞毒性T淋巴细胞相关抗原4(CTLA4)的剪接异构体。

Genetic variation in ICOS regulates mRNA levels of ICOS and splicing isoforms of CTLA4.

作者信息

Kaartinen Tanja, Lappalainen Jani, Haimila Katri, Autero Matti, Partanen Jukka

机构信息

Research and Development, Finnish Red Cross Blood Service, Kivihaantie 7, FI-00310 Helsinki, Finland.

出版信息

Mol Immunol. 2007 Mar;44(7):1644-51. doi: 10.1016/j.molimm.2006.08.010. Epub 2006 Sep 25.

Abstract

Genetic and functional studies suggest that polymorphism in cytotoxic T lymphocyte-associated antigen-4 (CTLA4) and inducible costimulator (ICOS) genes, both reported to harbour autoimmune susceptibility loci, could regulate the immune activation through affecting their expression and splicing of CTLA4. To address this, we studied expression of CTLA4 and ICOS and the role of polymorphisms in the gene region by measuring the relative amounts of transcripts, including the soluble CTLA4 (sCTLA4) splicing isoform in healthy volunteers. We combined a physiologically relevant in vitro activation for human CD4(+) T lymphocytes and a quantitative RT-PCR. The susceptibility allele CT60G in CTLA4 gene was confirmed to be associated with a decreased amount of sCTLA4, but only in resting cells. During the T cell activation two genetic variants in ICOS gene, IVS1+173T/C and c.1624C/T, affected expression of CTLA4 isoforms and ICOS, respectively. We could not confirm that the level of sCTLA4 is down-regulated following T lymphocyte activation, instead the levels of CTLA4 splicing isoforms correlated to each others. Our results indicate that genetic variation in this gene region regulates the expression of both CTLA4 and ICOS and not only the splicing of sCTLA4 as suggested earlier.

摘要

遗传和功能研究表明,细胞毒性T淋巴细胞相关抗原4(CTLA4)基因和诱导性共刺激分子(ICOS)基因的多态性可能通过影响CTLA4的表达和剪接来调节免疫激活,这两个基因均被报道含有自身免疫易感性位点。为了探究这一点,我们通过测量健康志愿者中包括可溶性CTLA4(sCTLA4)剪接异构体在内的转录本的相对含量,研究了CTLA4和ICOS的表达以及基因区域多态性的作用。我们将人CD4(+) T淋巴细胞的生理相关体外激活与定量逆转录聚合酶链反应(RT-PCR)相结合。CTLA4基因中的易感性等位基因CT60G被证实与sCTLA4含量降低有关,但仅在静息细胞中如此。在T细胞激活过程中,ICOS基因中的两个遗传变异体IVS1+173T/C和c.1624C/T分别影响了CTLA4异构体和ICOS的表达。我们无法证实T淋巴细胞激活后sCTLA4水平会下调,相反,CTLA4剪接异构体的水平相互关联。我们的结果表明,该基因区域的遗传变异调节了CTLA4和ICOS的表达,而不仅仅是如先前所示的sCTLA4的剪接。

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