Chandratilleke D, Hàla K, Marsh J A
Department of Microbiology and Immunology, Cornell University, Ithaca, NY 14850, USA.
Int J Immunopharmacol. 1996 Mar;18(3):203-10. doi: 10.1016/0192-0561(96)00010-0.
Cornell K strain chickens received a diet supplemented with 0, 0.1 and 1.0 ppm T3 from the day of hatching. At 28 days of age, splenocyte suspensions were prepared and analyzed by flow cytometry for interleukin-2 receptor (IL-2R) and CD3 expression. The low T3 dose increased the percentage of resting small cells expressing IL-2R while the mean fluorescence for this marker was enhanced only after mitogenic activation. This treatment did not alter the number of larger cells positive for IL-2R but did increase their mean fluorescence following mitogenic activation. The high T3 dose depressed the numbers of cells positive for IL-2R and their mean fluorescence amongst all splenocyte preparations. Both levels of T3 enhanced the numbers of CD3-positive cells in all cell preparations. These results suggest that the IL-2R expression can be modulated by in vivo T3 supplementation and that these correlate with the previously demonstrated changes in IL-2-like activity. The regulation of IL-2R expression provides one mechanism through which thyroid status may regulate immune function.
康奈尔K系鸡从孵化之日起接受添加了0、0.1和1.0 ppm三碘甲状腺原氨酸(T3)的日粮。在28日龄时,制备脾细胞悬液,并通过流式细胞术分析白细胞介素-2受体(IL-2R)和CD3的表达。低剂量T3增加了表达IL-2R的静止小细胞的百分比,而该标志物的平均荧光仅在有丝分裂原激活后增强。这种处理并未改变IL-2R阳性大细胞的数量,但在有丝分裂原激活后确实增加了它们的平均荧光。高剂量T3降低了所有脾细胞悬液中IL-2R阳性细胞的数量及其平均荧光。两种T3水平均增加了所有细胞悬液中CD3阳性细胞的数量。这些结果表明,体内补充T3可调节IL-2R的表达,且这些与先前证明的IL-2样活性变化相关。IL-2R表达的调节提供了一种甲状腺状态可能调节免疫功能的机制。