Stoecklein Veit M, Osuka Akinori, Ishikawa Shizu, Lederer Madeline R, Wanke-Jellinek Lorenz, Lederer James A
Department of Surgery, Brigham and Women's Hospital/Harvard Medical School, Boston, MA 02115.
Department of Surgery, Brigham and Women's Hospital/Harvard Medical School, Boston, MA 02115
J Immunol. 2015 Feb 1;194(3):1178-89. doi: 10.4049/jimmunol.1303051. Epub 2014 Dec 24.
Radiation exposure induces cell and tissue damage, causing local and systemic inflammatory responses. Because the inflammasome pathway is triggered by cell death and danger-associated molecular patterns, we hypothesized that the inflammasome may signal acute and chronic immune responses to radiation. Using a mouse radiation model, we show that radiation induces a dose-dependent increase in inflammasome activation in macrophages, dendritic cells, NK cells, T cells, and B cells as judged by cleaved caspase-1 detection in cells. Time course analysis showed the appearance of cleaved caspase-1 in cells by day 1 and sustained expression until day 7 after radiation. Also, cells showing inflammasome activation coexpressed the cell surface apoptosis marker annexin V. The role of caspase-1 as a trigger for hematopoietic cell losses after radiation was studied in caspase-1(-/-) mice. We found less radiation-induced cell apoptosis and immune cell loss in caspase-1(-/-) mice than in control mice. Next, we tested whether uric acid might mediate inflammasome activation in cells by treating mice with allopurinol and discovered that allopurinol treatment completely blocked caspase-1 activation in cells. Finally, we demonstrate that radiation-induced caspase-1 activation occurs by a Nod-like receptor family protein 3-independent mechanism because radiation-exposed Nlrp3(-/-) mice showed caspase-1 activation profiles that were indistinguishable from those of wild-type mice. In summary, our data demonstrate that inflammasome activation occurs in many immune cell types following radiation exposure and that allopurinol prevented radiation-induced inflammasome activation. These results suggest that targeting the inflammasome may help control radiation-induced inflammation.
辐射暴露会导致细胞和组织损伤,引发局部和全身炎症反应。由于炎性小体途径是由细胞死亡和危险相关分子模式触发的,我们推测炎性小体可能介导对辐射的急性和慢性免疫反应。使用小鼠辐射模型,我们发现,通过检测细胞中裂解的半胱天冬酶-1判断,辐射可导致巨噬细胞、树突状细胞、自然杀伤细胞、T细胞和B细胞中炎性小体激活呈剂量依赖性增加。时间进程分析显示,辐射后第1天细胞中出现裂解的半胱天冬酶-1,并持续表达至第7天。此外,显示炎性小体激活的细胞共表达细胞表面凋亡标志物膜联蛋白V。在半胱天冬酶-1基因敲除(caspase-1(-/-))小鼠中研究了半胱天冬酶-1作为辐射后造血细胞损失触发因素的作用。我们发现,与对照小鼠相比,caspase-1(-/-)小鼠辐射诱导的细胞凋亡和免疫细胞损失更少。接下来,我们通过用别嘌醇处理小鼠来测试尿酸是否可能介导细胞中的炎性小体激活,发现别嘌醇处理完全阻断了细胞中的半胱天冬酶-1激活。最后,我们证明辐射诱导的半胱天冬酶-1激活是通过一种不依赖Nod样受体家族蛋白3的机制发生的,因为接受辐射的Nlrp3(-/-)小鼠显示出与野生型小鼠无法区分的半胱天冬酶-1激活谱。总之,我们的数据表明,辐射暴露后多种免疫细胞类型中都会发生炎性小体激活,且别嘌醇可预防辐射诱导的炎性小体激活。这些结果表明,靶向炎性小体可能有助于控制辐射诱导的炎症。