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活性氧调节活化诱导的T细胞凋亡。

Reactive oxygen species regulate activation-induced T cell apoptosis.

作者信息

Hildeman D A, Mitchell T, Teague T K, Henson P, Day B J, Kappler J, Marrack P C

机构信息

Howard Hughes Medical Institute, Department of Medicine, National Jewish Medical and Research Center, Denver, Colorado 80206, USA.

出版信息

Immunity. 1999 Jun;10(6):735-44. doi: 10.1016/s1074-7613(00)80072-2.

Abstract

Reactive oxygen species (ROS) mediate apoptosis in a number of cell types. We studied the role that ROS play in activated T cell apoptosis by activating T cells in vivo and then culturing them for a short time. Activated T cells died independently of Fas and TNF alpha. Their death was characterized by rapid loss of mitochondrial transmembrane potential (delta psi(m)), caspase-dependent DNA fragmentation, and superoxide generation. A superoxide dismutase mimetic, Mn (III) tetrakis (5, 10, 15, 20-benzoic acid) porphyrin (MnTBAP), protected T cells from superoxide generation, caspase-dependent DNA loss, loss of delta psi(m), and cell death. These results indicate that ROS can regulate signals involved in caspase activation and apoptosis and may contribute to peripheral T cell deletion.

摘要

活性氧(ROS)介导多种细胞类型的凋亡。我们通过在体内激活T细胞,然后短期培养来研究ROS在活化T细胞凋亡中所起的作用。活化的T细胞独立于Fas和肿瘤坏死因子α(TNFα)而死亡。它们的死亡特征为线粒体跨膜电位(Δψm)迅速丧失、半胱天冬酶依赖性DNA片段化以及超氧化物生成。一种超氧化物歧化酶模拟物,四(5,10,15,20 - 苯甲酸)锰卟啉(MnTBAP),可保护T细胞免受超氧化物生成、半胱天冬酶依赖性DNA损失、Δψm丧失以及细胞死亡的影响。这些结果表明,ROS可调节参与半胱天冬酶激活和凋亡的信号,并且可能促成外周T细胞的清除。

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