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T细胞的逐步激活。钙离子载体A23187的作用。

Stepwise activation of T cells. Role of the calcium ionophore A23187.

作者信息

Geller R L, Gromo G, Inverardi L, Ferrero E, Bach F H

机构信息

Department of Laboratory of Medicine/Pathology and Surgery, University of Minnesota Hospital and Clinic, Minneapolis 55455.

出版信息

J Immunol. 1987 Dec 15;139(12):3930-4.

PMID:2826575
Abstract

The calcium ionophore A23187, at a concentration of 1 microgram/ml, is able to stimulate proliferation of freshly isolated peripheral blood lymphocytes, CD4+-enriched cells, or CD8+-enriched cells as measured by [3H]thymidine incorporation. This proliferation is accompanied by an increase in interleukin 2 (IL-2) receptor expression but not by a detectable up-regulation in (IL-2) production or the development of cytotoxicity. Proliferation can be blocked by anti-CD3, CD4, or CD8 monoclonal antibodies, but not by anti-Tac. If CD8+-enriched cells are activated for 3 days with A23187 and the blasts present on day 3 are sorted and returned to culture, they rapidly develop cytolytic activity in the presence of recombinant IL-2 but not recombinant interferon-gamma. CD4+ enriched cells, after activation with A23187, do not become cytotoxic in the presence of either recombinant IL-2 or recombinant interferon-gamma. These findings permit study of the stepwise maturation of T cells in this alternative pathway by using "minimal signals" that do not, by themselves and as used in these studies, stimulate precursor Tc to mature to full effector cytotoxic function. These findings are consistent with the model that A23187 drives T cells only part way along a pathway of maturation and that an additional second signal must be given to effect maturation of cytotoxic status.

摘要

钙离子载体A23187浓度为1微克/毫升时,能够刺激新鲜分离的外周血淋巴细胞、富含CD4⁺的细胞或富含CD8⁺的细胞增殖,增殖情况通过[³H]胸苷掺入法测定。这种增殖伴随着白细胞介素2(IL - 2)受体表达的增加,但未检测到IL - 2产生上调或细胞毒性的发展。增殖可被抗CD3、CD4或CD8单克隆抗体阻断,但不能被抗Tac阻断。如果用A23187将富含CD8⁺的细胞激活3天,对第3天出现的母细胞进行分选并放回培养,它们在重组IL - 2存在下会迅速产生溶细胞活性,但在重组干扰素 - γ存在下则不会。用A23187激活后,富含CD4⁺的细胞在重组IL - 2或重组干扰素 - γ存在下都不会产生细胞毒性。这些发现使得通过使用“最小信号”来研究T细胞在这一替代途径中的逐步成熟成为可能,在这些研究中,这些信号本身不会刺激前体细胞毒性T细胞成熟为完全效应细胞毒性功能。这些发现与以下模型一致,即A23187仅驱动T细胞沿着成熟途径走一部分,并且必须给予额外的第二个信号才能实现细胞毒性状态的成熟。

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