Ratikan Josephine A, Micewicz Ewa D, Xie Michael W, Schaue Dörthe
Department of Radiation Oncology, David Geffen School of Medicine, University of California at Los Angeles, CA, USA.
Department of Radiation Oncology, David Geffen School of Medicine, University of California at Los Angeles, CA, USA.
Cancer Lett. 2015 Nov 28;368(2):238-45. doi: 10.1016/j.canlet.2015.03.031. Epub 2015 Mar 25.
The ability to recognize and respond to universal molecular patterns on invading microorganisms allows our immune system to stay on high alert, sensing danger to our self-integrity. Our own damaged cells and tissues in pathological situations activate similar warning systems as microbes. In this way, the body is able to mount a response that is appropriate to the danger. Toll-like receptors are at the heart of this pattern recognition system that initiates innate pro-oxidant, pro-inflammatory signaling cascades and ultimately bridges recognition of danger to adaptive immunity. The acute inflammatory lesions that are formed segue into resolution of inflammation, repair and healing or, more dysfunctionally, into chronic inflammation, autoimmunity, excessive tissue damage and carcinogenesis. Redox is at the nexus of this decision making process and is the point at which ionizing radiation initially intercepts to trigger similar responses to self-damage. In this review we discuss our current understanding of how radiation-damaged cells interact with Toll-like receptors and how the immune systems interprets these radiation-induced danger signals in the context of whole-body exposures and during local tumor irradiation.
识别并应对入侵微生物上的通用分子模式的能力,使我们的免疫系统保持高度警惕,感知对自身完整性的威胁。在病理情况下,我们自身受损的细胞和组织会激活与微生物类似的警报系统。通过这种方式,身体能够做出与危险相适应的反应。Toll样受体是这种模式识别系统的核心,它启动先天性促氧化剂、促炎信号级联反应,并最终将危险识别与适应性免疫联系起来。形成的急性炎症病变会过渡到炎症消退、修复和愈合,或者更功能失调地发展为慢性炎症、自身免疫、过度组织损伤和致癌作用。氧化还原作用处于这个决策过程的核心,也是电离辐射最初拦截以触发对自身损伤类似反应的点。在这篇综述中,我们讨论了我们目前对辐射损伤细胞如何与Toll样受体相互作用,以及免疫系统如何在全身暴露和局部肿瘤照射的背景下解读这些辐射诱导的危险信号的理解。