Division of Cardiovascular Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.
Division of Anaesthesia, Department of Medicine, University of Cambridge, Addenbrooke's Hospital, Cambridge, CB2 0QQ, UK.
Immunity. 2019 Apr 16;50(4):1033-1042.e6. doi: 10.1016/j.immuni.2019.03.003. Epub 2019 Mar 26.
Ancient organisms have a combined coagulation and immune system, and although links between inflammation and hemostasis exist in mammals, they are indirect and slower to act. Here we investigated direct links between mammalian immune and coagulation systems by examining cytokine proproteins for potential thrombin protease consensus sites. We found that interleukin (IL)-1α is directly activated by thrombin. Thrombin cleaved pro-IL-1α at a site perfectly conserved across disparate species, indicating functional importance. Surface pro-IL-1α on macrophages and activated platelets was cleaved and activated by thrombin, while tissue factor, a potent thrombin activator, colocalized with pro-IL-1α in the epidermis. Mice bearing a mutation in the IL-1α thrombin cleavage site (R114Q) exhibited defects in efficient wound healing and rapid thrombopoiesis after acute platelet loss. Thrombin-cleaved IL-1α was detected in humans during sepsis, pointing to the relevance of this pathway for normal physiology and the pathogenesis of inflammatory and thrombotic diseases.
远古生物拥有一个综合的凝血和免疫系统,尽管在哺乳动物中炎症和止血之间存在联系,但它们是间接的,作用也比较缓慢。在这里,我们通过检查细胞因子原蛋白中可能存在的凝血酶蛋白酶共识位点,研究了哺乳动物免疫和凝血系统之间的直接联系。我们发现白细胞介素(IL)-1α可被凝血酶直接激活。凝血酶在不同物种中完全保守的位点切割 pro-IL-1α,表明其具有重要的功能。巨噬细胞和活化血小板表面的 pro-IL-1α被凝血酶切割和激活,而组织因子,一种有效的凝血酶激活剂,与表皮中的 pro-IL-1α共定位。在携带 IL-1α 凝血酶切割位点(R114Q)突变的小鼠中,在急性血小板减少后,其伤口愈合效率和快速血小板生成存在缺陷。在脓毒症患者中检测到凝血酶切割的 IL-1α,这表明该途径与正常生理学以及炎症和血栓形成性疾病的发病机制相关。