Boyapati Ray K, Tamborska Arina, Dorward David A, Ho Gwo-Tzer
MRC Centre for Inflammation Research Queens Medical Research Institute, University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK; Department of Gastroenterology, Monash Health, Clayton, VIC, Australia.
MRC Centre for Inflammation Research Queens Medical Research Institute, University of Edinburgh, 47 Little France Crescent, Edinburgh, EH16 4TJ, UK.
F1000Res. 2017 Feb 20;6:169. doi: 10.12688/f1000research.10397.1. eCollection 2017.
Mitochondrial DNA (mtDNA) has many similarities with bacterial DNA because of their shared common ancestry. Increasing evidence demonstrates mtDNA to be a potent danger signal that is recognised by the innate immune system and can directly modulate the inflammatory response. In humans, elevated circulating mtDNA is found in conditions with significant tissue injury such as trauma and sepsis and increasingly in chronic organ-specific and systemic illnesses such as steatohepatitis and systemic lupus erythematosus. In this review, we examine our current understanding of mtDNA-mediated inflammation and how the mechanisms regulating mitochondrial homeostasis and mtDNA release represent exciting and previously under-recognised important factors in many human inflammatory diseases, offering many new translational opportunities.
线粒体DNA(mtDNA)与细菌DNA有许多相似之处,因为它们有着共同的祖先。越来越多的证据表明,mtDNA是一种强大的危险信号,可被先天免疫系统识别,并能直接调节炎症反应。在人类中,循环mtDNA水平升高见于创伤和脓毒症等伴有严重组织损伤的情况,在脂肪性肝炎和系统性红斑狼疮等慢性器官特异性疾病和全身性疾病中也越来越常见。在这篇综述中,我们审视了目前对mtDNA介导的炎症的理解,以及调节线粒体稳态和mtDNA释放的机制如何在许多人类炎症性疾病中成为令人兴奋且此前未被充分认识的重要因素,从而带来了许多新的转化研究机会。