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首页> 外文期刊>American Journal of Transplantation >Liver Ischemia and Reperfusion Injury: New Insights into Mechanisms of Innate—Adaptive Immune-Mediated Tissue Inflammation
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Liver Ischemia and Reperfusion Injury: New Insights into Mechanisms of Innate—Adaptive Immune-Mediated Tissue Inflammation

机译:肝缺血和再灌注损伤:对先天的适应性免疫介导的组织炎症机制的新见解。

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摘要

Ischemia and reperfusion injury (IRI) is a dynamic process that involves two distinctive yet interrelated phases of ischemic organ damage and inflammation-mediated reperfusion injury. Although multiple cellular and molecular pathways contribute and regulate tissue/organ damage, integration of different players into a unified mechanism is warranted. The crosstalk between innate and adaptive immune systems plays a significant role in the pathogenesis of liver IRI. In this review, we focus on recent progress in the mechanism of liver innate immune activation by IR. Kupffer cells (KC), DCs, NK, as well as T cells initiate local inflammation response, the hallmark of IRI, by utilizing distinctive immune receptors to recognize and/or trigger various molecules, both endogenous and exogenous. The interlocked molecular signaling pathways in the context of multiple liver cell types, the IRI kinetics and positive versus negative regulatory loops in the innate immune activation process are discussed. Better appreciation of molecular interactions that mediate these intricate cascades, should allow for the development of novel therapeutic approached against IRI in liver transplant recipients.
机译:缺血和再灌注损伤(IRI)是一个动态过程,涉及缺血器官损害和炎症介导的再灌注损伤两个不同但相互关联的阶段。尽管多种细胞和分子途径有助于并调节组织/器官损伤,但仍需要将不同参与者整合到一个统一的机制中。先天性免疫系统和适应性免疫系统之间的串扰在肝脏IRI的发病机理中起着重要作用。在这篇综述中,我们关注于IR对肝脏固有免疫激活机制的最新进展。枯否细胞(KC),DC,NK和T细胞通过利用独特的免疫受体识别和/或触发内源性和外源性各种分子来启动局部炎症反应(IRI的标志)。讨论了多种肝细胞类型,IRI动力学以及先天性免疫激活过程中的正负调节环的互锁分子信号通路。更好地理解介导这些复杂级联反应的分子相互作用,应该允许开发针对肝移植接受者中针对IRI的新型治疗方法。

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