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The DNA damage response: a common pathway in the regulation of NKG2D and DNAM-1 ligand expression in normal, infected, and cancer cells

机译:DNA损伤反应:调控正常,感染和癌细胞中NKG2D和DNAM-1配体表达的常见途径

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摘要

NKG2D and DNAM-1 are two activating receptors, present on the surface of NK cells and other cells of the immune system. Their ligands - MICA, MICB, ULBP1-6 for NKG2D, PVR/CD155 and Nectin-2/CD112 for DNAM-1 - can be constitutively expressed at low levels in some normal cells, but they are more often defined as "stress-induced," since different stimuli can positively regulate their expression. In this review, we describe the molecular mechanisms involved in the up-regulation of NKG2D and DNAM-1 ligands under different physiological and pathological "stress" conditions, including mitosis, viral infections, and cancer. We will focus on the DNA damage response, as recent advances in the field have uncovered its important role as a common signaling pathway in the regulation of both NKG2D and DNAM-1 ligand expression in response to very diverse conditions and stimuli.
机译:NKG2D和DNAM-1是两种激活受体,存在于NK细胞和免疫系统其他细胞的表面。它们的配体-NKG2D的MICA,MICB,ULBP1-6,DNAM-1的PVR / CD155和Nectin-2 / CD112-可以在某些正常细胞中低水平组成型表达,但它们通常被定义为“应激诱导的” ”,因为不同的刺激可以积极调节其表达。在这篇综述中,我们描述了在不同的生理和病理“应激”条件(包括有丝分裂,病毒感染和癌症)下,NKG2D和DNAM-1配体上调的分子机制。我们将专注于DNA损伤反应,因为该领域的最新进展已经揭示了其作为常见信号通路在调节NKG2D和DNAM-1配体表达以响应多种多样的条件和刺激中的重要作用。

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