Thurairajah Kabilan, Briggs Gabrielle Daisy, Balogh Zsolt Janos
Department of Traumatology, John Hunter Hospital and University of Newcastle, Newcastle, NSW, Australia.
Eur J Trauma Emerg Surg. 2018 Jun;44(3):325-334. doi: 10.1007/s00068-018-0954-3. Epub 2018 Apr 9.
Mitochondria play a key role in the pathophysiology of post-injury inflammation. Cell-free mitochondrial DNA (cf-mtDNA) is now understood to catalyse sterile inflammation after trauma. Observations in trauma cohorts have identified high cf-mtDNA in patients with systemic inflammatory response syndrome and multiple organ failure as well as following major surgery. The source of cf-mtDNA can be various cells affected by mechanical and hypoxic injury (passive mechanism) or induced by inflammatory mechanisms (active mechanism). Multiple forms of cf-mtDNA exist; mtDNA fragments, mtDNA in microparticles/vesicles and cell-free mitochondria. Trauma to cells that are rich in mitochondria are believed to release more cf-mtDNA. This review describes the current understanding of the mechanisms of cf-mtDNA release, its systemic effects and the potential therapeutic implications related to its modification. Although current understanding is insufficient to change trauma management, focussed research goals have been identified to pave the way for monitoring and manipulation of cf-mtDNA release and effects in trauma.
线粒体在损伤后炎症的病理生理学中起关键作用。现在已知无细胞线粒体DNA(cf-mtDNA)会在创伤后引发无菌性炎症。对创伤队列的观察发现,全身炎症反应综合征和多器官功能衰竭患者以及大手术后患者的cf-mtDNA水平较高。cf-mtDNA的来源可以是受机械和缺氧损伤影响的各种细胞(被动机制),也可以是由炎症机制诱导产生的(主动机制)。cf-mtDNA存在多种形式;线粒体DNA片段、微粒/囊泡中的线粒体DNA以及无细胞线粒体。富含线粒体的细胞受到创伤后,据信会释放更多的cf-mtDNA。本综述描述了目前对cf-mtDNA释放机制、其全身效应以及与其修饰相关的潜在治疗意义的理解。尽管目前的认识还不足以改变创伤管理,但已确定了重点研究目标,为监测和控制创伤中cf-mtDNA的释放及其效应铺平道路。