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1,25-二羟维生素D3对白细胞介素-1生成的抑制作用。

Inhibition of interleukin-1 production by 1,25-dihydroxyvitamin D3.

作者信息

Tsoukas C D, Watry D, Escobar S S, Provvedini D M, Dinarello C A, Hustmyer F G, Manolagas S C

机构信息

Department of Biology, San Diego State University, California 92182.

出版信息

J Clin Endocrinol Metab. 1989 Jul;69(1):127-33. doi: 10.1210/jcem-69-1-127.

Abstract

The hormonal form of vitamin D, 1,25-dihydroxyvitamin D3 [1,25-(OH)2D3], inhibits the proliferation of T lymphocytes and production of growth-promoting factors (including interleukin-2) (IL2) in CTLL2 murine cells. In this study, we investigated the role of monocytes in this hormone-mediated inhibitory effect, by testing the effects of 1,25-(OH)2D3 on the ability of the mitogenic lectin phytohemagglutinin (PHA) to induce T cell activation in either a monocyte-dependent or phorbol myristate acetate (PMA)-driven (monocyte-independent) system. The results indicate that proliferation of T cells and production of growth-promoting factors are inhibited by 1,25-(OH)2D3 only in the monocyte-dependent system. Preincubation of monocytes with 1,25-(OH)2D3 for various periods of time and subsequent removal of the hormone resulted in inhibition of the PHA-driven proliferation of T cells. Preincubation for 2 h resulted in 20% inhibition, while preincubation for 36 h reduced proliferation to 50% of the control value [no 1,25-(OH)2D3 exposure]. These data suggested that monocytes are important participants in 1,25-(OH)2D3-mediated events. Therefore, we tested the effects of the hormone on the production of IL1, a monocyte-derived product thought to be involved in the induction of IL2 release and the subsequent development of the T cell proliferative response. 1,25-(OH)2D3 inhibited the production of both extracellular and cell-associated immunoreactive IL1 alpha and IL1 beta. Indomethacin, a prostaglandin synthetase inhibitor, did not alter the inhibitory properties of 1,25-(OH)2D3, suggesting that prostaglandins are not responsible for the inhibitory phenomenon. We conclude that part of the ability of 1,25-(OH)2D3 to inhibit T cell proliferation may be due to direct effects on monocytes by down-regulating IL-1 production. However, it is unlikely that the immunoregulatory properties of 1,25-(OH)2D3 on T cells are mediated solely through monocytes, and it is possible that the hormone also exerts its influence directly on T cells.

摘要

维生素D的激素形式,即1,25 - 二羟基维生素D3 [1,25-(OH)2D3],可抑制CTLL2小鼠细胞中T淋巴细胞的增殖以及生长促进因子(包括白细胞介素-2)(IL2)的产生。在本研究中,我们通过检测1,25-(OH)2D3对促有丝分裂凝集素植物血凝素(PHA)在单核细胞依赖或佛波酯肉豆蔻酸酯(PMA)驱动(单核细胞非依赖)系统中诱导T细胞活化能力的影响,来研究单核细胞在这种激素介导的抑制作用中的作用。结果表明,仅在单核细胞依赖系统中,1,25-(OH)2D3可抑制T细胞增殖和生长促进因子的产生。用1,25-(OH)2D3对单核细胞进行不同时间段的预孵育,随后去除该激素,导致PHA驱动的T细胞增殖受到抑制。预孵育2小时导致20%的抑制率,而预孵育36小时则使增殖降至对照值(未暴露于1,25-(OH)2D3)的50%。这些数据表明单核细胞是1,25-(OH)2D3介导事件的重要参与者。因此,我们检测了该激素对IL1产生的影响,IL1是一种单核细胞衍生产物,被认为参与IL2释放的诱导以及随后T细胞增殖反应的发展。1,25-(OH)2D3抑制细胞外和细胞相关免疫反应性IL1α和IL1β的产生。前列腺素合成酶抑制剂吲哚美辛并未改变1,25-(OH)2D3的抑制特性,这表明前列腺素并非这种抑制现象的原因。我们得出结论,1,25-(OH)2D3抑制T细胞增殖的部分能力可能是由于通过下调IL - 1产生而对单核细胞产生的直接作用。然而,1,25-(OH)2D3对T细胞的免疫调节特性不太可能仅通过单核细胞介导,并且该激素也有可能直接对T细胞发挥其影响。

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