Department of Neurology, Beijing Anzhen Hospital, Capital Medical University, Beijing, 100029, China.
Department of Neurology, Peking University People's Hospital, Beijing, 100044, China.
Cell Mol Neurobiol. 2019 Apr;39(3):451-460. doi: 10.1007/s10571-019-00661-z. Epub 2019 Feb 18.
Various studies demonstrate that CD137 (TNFRSF9, 4-1BB) promotes atherosclerosis and vascular inflammation in experimental models via interactions with the CD137 ligand (CD137L). However, the exact role of CD137 in ischemic stroke remains unclear. In this study, we analyzed dynamic changes of peripheral CD137 expression on T cells in a mouse model of cerebral ischemia-middle cerebral artery occlusion (MCAO), as well as alternation of neurological function, infarct size and cerebral inflammatory status after inhibition of the CD137/CD137L pathway using an anti-CD137L monoclonal antibody. MCAO mice showed elevated surface expression of CD137 on T cells in both peripheral blood and lymphoid tissues during early cerebral ischemia. Remarkably, blockade of the CD137/CD137L pathway reduced the post-ischemic brain damage. Our findings indicate that enhanced CD137 costimulation occurs in early cerebral ischemia and promotes T cell activation, which in turn upregulates inflammatory immune response and possibly exerting deleterious effects on cerebral ischemia.
多种研究表明,CD137(TNFRSF9,4-1BB)通过与 CD137 配体(CD137L)相互作用,促进实验模型中的动脉粥样硬化和血管炎症。然而,CD137 在缺血性中风中的确切作用仍不清楚。在本研究中,我们分析了脑缺血-大脑中动脉闭塞(MCAO)小鼠模型中 T 细胞外周 CD137 表达的动态变化,以及使用抗 CD137L 单克隆抗体抑制 CD137/CD137L 通路后神经功能、梗死面积和脑炎症状态的改变。MCAO 小鼠在早期脑缺血期间外周血和淋巴组织中的 T 细胞表面 CD137 表达升高。值得注意的是,阻断 CD137/CD137L 通路可减轻缺血后的脑损伤。我们的研究结果表明,早期脑缺血中增强的 CD137 共刺激作用促进了 T 细胞的激活,进而上调了炎症免疫反应,可能对脑缺血产生有害影响。