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在自然杀伤细胞细胞毒性试验中,用白细胞介素-2或地塞米松对人外周血淋巴细胞进行预处理,不会改变它们对甲硫氨酸脑啡肽的反应。

Pretreatment of human peripheral blood lymphocytes with interleukin-2 or dexamethasone does not alter their response to Met-Enkephalin in a NK-cytotoxic assay.

作者信息

Martin-Kleiner I, Gabrilovac J

机构信息

Ruder Bosković Institute, Department of Biology and Medicine, Zagreb, Croatia.

出版信息

Immunopharmacol Immunotoxicol. 1996 Feb;18(1):37-57. doi: 10.3109/08923979609007109.

Abstract

The effect of Met-Enkephalin (MENK; 10(-12) - 10(-8) M) on NK-activity of peripheral blood lymphocytes (PBL) after in vitro treatment (18 h, 37 degrees C) was examined in 30 young, healthy male donors. In the group as a whole (n = 30), no significant effect of MENK was detected. At the individual level, 18 of 30 donors (60%) responded to MENK either by mild enhancement (up to 8%, 8 responders), or by mild attenuation (up to 12%, 10 responders) of the basal NK-activity. The effect of MENK was donor-related regarding the dose-response, E/T ratio, and direction of MENK action. The influence of pretreatment of PBL (1 h) with either graded doses of interleukin-2 (IL-2; 3, 25, 50 U/ml) or dexamethasone (Dex; 2.5 x 10(-9), 2.5 x 10(-8), 2.5 x 10(-7) M), on the effect of MENK was also tested. The idea was that pretreatment of PBL would result in predictable, and/or stronger response to MENK. In the group as a whole again no significant effect of MENK was detected on the NK-activity of PBL prestimulated by IL-2 (n = 16), or inhibited by Dex (n = 12). Further, pretreatment of PBL with IL-2/Dex did not significantly alter the intensity of modulation by MENK, which was generally mild. The data obtained have shown that pretreatment of PBL with IL-2 or Dex, regardless of their concentrations, did not significantly alter the frequency of responders to MENK being 50%, 62.5% and 64.3% with 3, 25 or 50 U/ml IL-2, respectively, and 50% with all concentration of Dex used, as compared to that observed with resting PBL (60%). However, at the individual level physiological concentrations of MENK (10(-12) - 10(-9) M) induced enhancement or/and attenuation of the NK-activity pretreated with IL-2/Dex, respectively. The effect of MENK at the individual level was donor-related regarding the dose-response, E/T ratio, and direction of MENK action. Thus, pretreatment of PBL with graded concentrations of IL-2/Dex did not alter the effect of MENK on NK-activity, regarding the frequency and intensity, as well as the direction of modulation: it remained bidirectional, of low intensity, and independent of the grade of PBL preactivation/inhibition, therefore unpredictable.

摘要

在30名年轻、健康的男性献血者中,检测了甲硫氨酸脑啡肽(MENK;10⁻¹² - 10⁻⁸ M)在体外处理(18小时,37℃)后对外周血淋巴细胞(PBL)自然杀伤(NK)活性的影响。在整个组(n = 30)中,未检测到MENK有显著影响。在个体水平上,30名献血者中有18名(60%)对MENK有反应,表现为基础NK活性轻度增强(高达8%,8名反应者)或轻度减弱(高达12%,10名反应者)。MENK的作用在剂量反应、效靶比和作用方向方面与献血者相关。还测试了用不同剂量的白细胞介素-2(IL-2;3、25、50 U/ml)或地塞米松(Dex;2.5×10⁻⁹、2.5×10⁻⁸、2.5×10⁻⁷ M)对PBL进行预处理(1小时)对MENK作用的影响。其想法是PBL的预处理将导致对MENK产生可预测的和/或更强的反应。在整个组中,同样未检测到MENK对经IL-2刺激(n = 16)或经Dex抑制(n = 12)的PBL的NK活性有显著影响。此外,用IL-2/Dex对PBL进行预处理并未显著改变MENK的调节强度,这种调节通常是轻微的。所获得的数据表明,用IL-2或Dex对PBL进行预处理,无论其浓度如何,与静息PBL(60%)相比,用3、25或50 U/ml IL-2预处理时对MENK有反应者的频率分别为50%、62.5%和64.3%,用所有使用浓度的Dex预处理时为50%,均未显著改变。然而,在个体水平上,生理浓度的MENK(10⁻¹² - 10⁻⁹ M)分别诱导了经IL-2/Dex预处理的NK活性增强或/和减弱。MENK在个体水平上的作用在剂量反应、效靶比和作用方向方面与献血者相关。因此,用不同浓度的IL-2/Dex对PBL进行预处理,在频率、强度以及调节方向方面,并未改变MENK对NK活性的作用:它仍然是双向的、低强度的,并且与PBL预激活/抑制的程度无关,因此是不可预测的。

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