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通过葡萄球菌肠毒素依赖性细胞介导的细胞毒性作用,在用γ干扰素处理的小鼠腹膜巨噬细胞中观察到细胞凋亡。

Apoptosis observed in murine peritoneal macrophages treated with interferon gamma through staphylococcal enterotoxin-dependent cell-mediated cytotoxicity.

作者信息

Sakurada J, Tajima A, Shinji H, Seki K, Masuda S

机构信息

Department of Microbiology (II), Jikei University School of Medicine, Tokyo, Japan.

出版信息

Microbiol Immunol. 2000;44(12):1063-6. doi: 10.1111/j.1348-0421.2000.tb02603.x.

Abstract

The concept of superantigens is well-known and widely accepted. In this brief communication, we analyze the behaviour of antigen-presenting cells after T-cell activation by staphylococcal enterotoxin B, a representative superantigen. We tried to activate murine T cells by inflammatory mouse peritoneal macrophage in the presence of staphylococcal enterotoxin B, but no T-cell activation was observed. We, therefore, analyzed surface-specific antigens of the macrophages. They expressed insufficient amounts of MHC class II, CD80 and CD86 molecules on the surface of the cells. On the contrary, increased amounts of MHC class II and CD86 molecules on the cell surfaces were observed after incubation with interferon gamma. Interferon gamma-primed macrophages were found to be competent to activate T cells in the presence of staphylococcal enterotoxin B. To our surprise, these macrophages underwent apoptosis in parallel with T-cell activation.

摘要

超抗原的概念广为人知且被广泛接受。在这篇简短的通讯中,我们分析了代表性超抗原——葡萄球菌肠毒素B激活T细胞后抗原呈递细胞的行为。我们试图在葡萄球菌肠毒素B存在的情况下,通过炎性小鼠腹腔巨噬细胞激活小鼠T细胞,但未观察到T细胞激活。因此,我们分析了巨噬细胞的表面特异性抗原。它们在细胞表面表达的MHC II类、CD80和CD86分子数量不足。相反,用干扰素γ孵育后,细胞表面的MHC II类和CD86分子数量增加。发现用干扰素γ预处理的巨噬细胞在葡萄球菌肠毒素B存在的情况下能够激活T细胞。令我们惊讶的是,这些巨噬细胞在T细胞激活的同时发生了凋亡。

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