Institut de Génétique Humaine, CNRS, Université de Montpellier, Equipe Labellisée Ligue contre le Cancer, Montpellier France.
Institut de Génétique Humaine, CNRS, Université de Montpellier, Equipe Labellisée Ligue contre le Cancer, Montpellier France.
Curr Opin Immunol. 2019 Feb;56:24-30. doi: 10.1016/j.coi.2018.09.017. Epub 2018 Oct 5.
Cytosolic DNA of endogenous or exogenous origin is sensed by the cGAS-STING pathway to activate innate immune responses. Besides microbial DNA, this pathway detects self-DNA in the cytoplasm of damaged or abnormal cells and plays a central role in antitumor immunity. The mechanism by which cytosolic DNA accumulates under genotoxic stress conditions is currently unclear, but recent studies on factors mutated in the Aicardi-Goutières syndrome cells, such as SAMHD1, RNase H2 and TREX1, are shedding new light on this key process. In particular, these studies indicate that the rupture of micronuclei and the release of ssDNA fragments during the processing of stalled replication forks and chromosome breaks represent potent inducers of the cGAS-STING pathway.
内源性或外源性来源的细胞质 DNA 通过 cGAS-STING 途径被感知,从而激活先天免疫反应。除了微生物 DNA 之外,该途径还能在受损或异常细胞的细胞质中检测到自身 DNA,并在抗肿瘤免疫中发挥核心作用。目前尚不清楚在遗传毒性应激条件下细胞质 DNA 积累的机制,但最近对 Aicardi-Goutières 综合征细胞中突变的因素(如 SAMHD1、RNase H2 和 TREX1)的研究为这一关键过程提供了新的线索。特别是,这些研究表明,在停滞复制叉和染色体断裂的处理过程中微核的破裂和 ssDNA 片段的释放是 cGAS-STING 途径的有效诱导剂。