Department of Neurology, Peking University People's Hospital, Beijing, China.
Department of Neurology, Beijing Anzhen Hospital, Capital Medical University, Beijing, China.
Clin Transl Sci. 2018 Jul;11(4):428-434. doi: 10.1111/cts.12553. Epub 2018 Apr 26.
As a proinflammatory cytokine, CD137 (4-1BB, TNFRSF9) is present in membrane-bound and soluble forms. Increased expression of CD137 was recently found in T cells in human atherosclerotic plaques. However, the exact role of CD137 in ischemic stroke is not clear. In this study we analyzed the protein levels of soluble CD137 (sCD137) and the expression of CD137 on CD4+ T cells in the peripheral blood of patients with acute atherothrombotic stroke by using the cytometry beads array (CBA) and flow cytometry. Within 24 hours of onset, the stroke patients showed elevated levels of sCD137 (2.7 pg/ml) and CD137 expression on CD4+ T cells (4.9 ± 3.2%) compared with normal controls (1.1 pg/ml, P < 0.01; 1.3 ± 1.0%, P < 0.01). Alterations in CD137 expression may enhance ischemia-induced inflammatory responses via bidirectional signaling and, consequently, aggravate brain injury in early stages of this disorder.
作为一种促炎细胞因子,CD137(4-1BB,TNFRSF9)以膜结合和可溶性形式存在。最近在人类动脉粥样硬化斑块中的 T 细胞中发现 CD137 的表达增加。然而,CD137 在缺血性中风中的确切作用尚不清楚。在这项研究中,我们使用细胞术珠阵列(CBA)和流式细胞术分析了急性动脉血栓性中风患者外周血中可溶性 CD137(sCD137)的蛋白水平和 CD4+T 细胞上的 CD137 表达。在发病后 24 小时内,中风患者的 sCD137 水平(2.7 pg/ml)和 CD4+T 细胞上的 CD137 表达(4.9 ± 3.2%)均高于正常对照组(1.1 pg/ml,P < 0.01;1.3 ± 1.0%,P < 0.01)。CD137 表达的改变可能通过双向信号增强缺血诱导的炎症反应,从而在这种疾病的早期阶段加重脑损伤。