Cerboni Cristina, Fionda Cinzia, Soriani Alessandra, Zingoni Alessandra, Doria Margherita, Cippitelli Marco, Santoni Angela
Department of Molecular Medicine, Istituto Pasteur-Fondazione Cenci Bolognetti, "Sapienza" University of Rome , Rome , Italy.
Laboratory of Immunoinfectivology, Bambino Gesù Children's Hospital, IRCCS , Rome , Italy.
Front Immunol. 2014 Jan 7;4:508. doi: 10.3389/fimmu.2013.00508.
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.
NKG2D和DNAM-1是两种激活受体,存在于自然杀伤细胞(NK细胞)及免疫系统的其他细胞表面。它们的配体——NKG2D的配体为MICA、MICB、ULBP1 - 6,DNAM-1的配体为PVR/CD155和Nectin-2/CD112——在一些正常细胞中可低水平组成性表达,但它们更常被定义为“应激诱导型”,因为不同刺激可正向调节其表达。在本综述中,我们描述了在不同生理和病理“应激”条件下,包括有丝分裂、病毒感染和癌症,NKG2D和DNAM-1配体上调所涉及的分子机制。我们将聚焦于DNA损伤反应,因为该领域的最新进展揭示了其作为一种共同信号通路在响应非常多样的条件和刺激时调节NKG2D和DNAM-配体表达中的重要作用。