依赖甲状腺素的自然杀伤活性调节。

Journal of Experimental Pathology Pub Date : 1987-01-01
M Provinciali, M Muzzioli, N Fabris
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引用次数: 0

摘要

在51cr释放实验中,以YAC-1为靶细胞,分析了甲状腺激素“体外”治疗对Balb/c小鼠基础或淋巴因子诱导的NK细胞毒性的影响。IFN或IL-2“体外”处理可显著增加中青年小鼠脾细胞的天然细胞毒活性。当两种淋巴因子同时施用时,观察到加性效应。“体外”脾细胞经甲状腺素预孵育可增加IFN诱导的NK细胞毒性活性,但不改变基础活性或IL-2诱导的NK细胞毒性活性。此外,甲状腺素能够显著增强IFN和IL-2同时加入诱导的最大促进作用。这些发现表明甲状腺激素在调节自然细胞介导的城市毒性,特别是NK细胞对IFN敏感性的表达中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Thyroxine-dependent modulation of natural killer activity.

The influence of "in vitro" treatment with thyroia hormones on basal or lymphokine-induced NK cytotoxicity was analyzed in Balb/c mice using YAC-1 as target cells in a 51 Cr release assay. "In vitro" treatment with IFN or IL-2 causes a considerable increase of the natural cytotoxic activity of spleen cells from young-middle aged mice. An additive effect is observed when the two lymphokines are administered simultaneously. "In vitro" spleen cells preincubation with thyroxine increases NK citotoxic activity induced by IFN but it does not modify the basal activity or that induced by IL-2. Furthermore, thyroxine was able to significantly amplify even the maximal boosting effect induced by the simultaneous addition of both IFN and IL-2. These findings suggest a role for thyroid hormones in the modulation of natural cell-mediated citotoxicity and particularly in the espression of NK cell sensitivity to IFN.

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