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DNA甲基化在自然杀伤细胞中克隆性分布的杀伤细胞免疫球蛋白样受体表达模式的决定中起关键作用。

Crucial role of DNA methylation in determination of clonally distributed killer cell Ig-like receptor expression patterns in NK cells.

作者信息

Santourlidis Simeon, Trompeter Hans-Ingo, Weinhold Sandra, Eisermann Britta, Meyer Klaus L, Wernet Peter, Uhrberg Markus

机构信息

Institute for Transplantation Diagnostics and Cell Therapeutics, Heinrich Heine University, Moorenstrasse 5, D-40225 Dusseldorf, Germany.

出版信息

J Immunol. 2002 Oct 15;169(8):4253-61. doi: 10.4049/jimmunol.169.8.4253.

Abstract

Human NK cells are characterized by the expression of surface receptors of the killer cell Ig-like receptor (KIR) family, which are involved in the specific recognition of pathogenic target cells. Each NK cell expresses and maintains an individual subset of inhibitory and stimulatory KIR and in this way contributes to a diversified NK cell repertoire. To date, the molecular basis for generation of clonally distributed KIR expression patterns has been elusive. Here, analyses of DNA methylation patterns of KIR genes in NK cell lines as well as in NK cells, freshly isolated from peripheral blood, demonstrated that a small CpG island surrounding the transcriptional start site of each KIR gene is consistently demethylated in expressed KIR and methylated in unexpressed KIR. DNA-demethylating treatment resulted in a rapid and stable induction of transcription and cell surface expression of all formerly unexpressed KIR in NK cell lines, NK cell clones, and freshly isolated NK cells, but not in other cell types. In vitro methylation of KIR CpG islands repressed reporter gene expression in NK cells. We conclude that clonal patterns of KIR expression are mainly epigenetically determined and maintained through DNA methylation.

摘要

人类自然杀伤细胞(NK细胞)的特征是表达杀伤细胞免疫球蛋白样受体(KIR)家族的表面受体,这些受体参与对致病性靶细胞的特异性识别。每个NK细胞表达并维持抑制性和刺激性KIR的一个单独亚群,以此促成多样化的NK细胞库。迄今为止,克隆分布的KIR表达模式产生的分子基础一直难以捉摸。在此,对NK细胞系以及从外周血中新鲜分离出的NK细胞中KIR基因的DNA甲基化模式分析表明,每个KIR基因转录起始位点周围的一个小CpG岛在表达的KIR中始终处于去甲基化状态,而在未表达的KIR中处于甲基化状态。DNA去甲基化处理导致NK细胞系、NK细胞克隆和新鲜分离的NK细胞中所有先前未表达的KIR的转录和细胞表面表达快速且稳定地诱导,但在其他细胞类型中则不然。KIR CpG岛的体外甲基化抑制了NK细胞中报告基因的表达。我们得出结论,KIR表达的克隆模式主要由表观遗传决定,并通过DNA甲基化得以维持。

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