Salminen Antero, Suuronen Tiina, Huuskonen Jari, Kaarniranta Kai
Department of Neuroscience and Neurology, University of Kuopio, P.O. Box 1627, FIN-70211 Kuopio, Finland.
Biochem Biophys Res Commun. 2008 Mar 21;367(4):715-8. doi: 10.1016/j.bbrc.2007.11.189. Epub 2008 Jan 15.
Activation of NF-kappaB transcription factor signaling is one of the hallmarks of genotoxic stress. Recently, the NEMO shuttle was revealed to mediate this nucleo-cytoplasmic signaling linking DNA damage to the activation of NF-kappaB system. DNA damage is the causative factor of several segmental progeroid syndromes, such as Werner syndrome and Hutchinson-Gilford syndrome. Although the gene defects have been well characterized, the molecular mechanisms of premature aging process still need to be defined. Here we review the details of the NEMO shuttle, a dual-signal sensor linking DNA damage to NF-kappaB activation, and present evidence for the hypothesis that DNA damage in progeroid syndromes may activate the NEMO shuttle and subsequently increase the pressure on the activation of NF-kappaB system evoking a premature aging phenotype. The NEMO shuttle may link genotoxic stress to the activation of the innate immunity system and cause premature aging via inflamm-aging process.
NF-κB转录因子信号的激活是基因毒性应激的标志之一。最近,人们发现NEMO穿梭蛋白介导这种核质信号传导,将DNA损伤与NF-κB系统的激活联系起来。DNA损伤是几种节段性早衰综合征的致病因素,如沃纳综合征和哈钦森-吉尔福德综合征。尽管基因缺陷已得到充分表征,但早衰过程的分子机制仍有待确定。在此,我们综述了NEMO穿梭蛋白的细节,它是一种将DNA损伤与NF-κB激活联系起来的双信号传感器,并为以下假设提供证据:早衰综合征中的DNA损伤可能激活NEMO穿梭蛋白,随后增加NF-κB系统激活的压力,从而引发早衰表型。NEMO穿梭蛋白可能将基因毒性应激与先天免疫系统的激活联系起来,并通过炎症衰老过程导致早衰。