Sahin Umut, Lallemand-Breitenbach Valérie, de Thé Hugues
Université Paris Diderot, Sorbonne Paris Cité, Hôpital St. Louis, Paris, France; INSERM UMR 944, Equipe Labellisée par la Ligue Nationale Contre le Cancer, Institut Universitaire d'Hématologie, Hôpital St. Louis, Paris, France; CNRS UMR 7212, Hôpital St. Louis, Paris, France.
J Pathol. 2014 Nov;234(3):289-91. doi: 10.1002/path.4426.
PML nuclear bodies (NBs) were first described by electron microscopy and rediscovered through their treatment-reversible disruption in a rare leukaemia. They recruit multiple partner proteins and now emerge as interferon- and oxidative stress-responsive sumoylation factories. NBs mediate interferon-induced viral restriction, enhance proteolysis, finely tune metabolism and enforce stress-induced senescence. Apart from being markers of cellular stress, PML NBs could be harnessed pharmacologically in a number of conditions, including cancer, viral infection or neurodegenerative diseases.
早幼粒细胞白血病核体(NBs)最初是通过电子显微镜描述的,并在一种罕见白血病中因其治疗可逆性破坏而被重新发现。它们招募多种伴侣蛋白,如今作为干扰素和氧化应激反应性SUMO化工厂出现。核体介导干扰素诱导的病毒限制、增强蛋白水解、精细调节代谢并引发应激诱导的衰老。除了作为细胞应激的标志物外,早幼粒细胞白血病核体在许多疾病状态下,包括癌症、病毒感染或神经退行性疾病中,都可以通过药物进行调控。