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白细胞介素-15可增强蜕膜淋巴细胞中短期细胞溶解介质的表达。

Short-term cytolytic mediators' expression in decidual lymphocytes is enhanced by interleukin-15.

作者信息

Strbo Natasa, Laskarin Gordana, Bogovic Crncic Tatjana, Juretic Frankovic Koraljka, Bedenicki Ivica, Sotosek Tokmadzic Vlatka, Randic Ljiljana, Le Bouteiller Philippe, Tabiasco Julie, Podack Eckhard R, Rukavina Daniel

机构信息

Department of Physiology and Immunology, Medical Faculty, University of Rijeka, Rijeka, Croatia.

出版信息

Am J Reprod Immunol. 2006 Mar;55(3):217-25. doi: 10.1111/j.1600-0897.2005.00351.x.

Abstract

PROBLEM

We investigated whether decidual adherent cells (DAC) and interleukin (IL)-15, in comparison to interleukin (IL)-2 affect cytolytic potential of first trimester decidual lymphocytes (DL).

METHOD OF STUDY

Decidual mononuclear cells were obtained by enzymatic digestion and density gradient centrifugation. Non-adherent DL were collected after 2-hr adherence and cultured for 18 or 72 hr with: IL-15 (0.5-5 ng/mL), IL-2 (100-1000 U/mL) or both of these cytokines, DAC (ratio 3:1 and 1:1) or DAC and anti-IL-15 antibody. Perforin, Fas ligand (FasL) and granzyme B were detected at mRNA level in indicated culture conditions. Cytolytic activity of DL against K-562, P815 and P815-Fas was measured by 2-hr PKH-26 cytotoxicity assay. The dynamics of perforin protein and mRNA expression were measured in DL after a contact with K-562 targets.

RESULTS

Interleukin-15 enhanced perforin, FasL and granzyme B transcription after 18-hr culture and prevented perforin protein downregulation, observed after DL culture. IL-2 had similar effects. DAC sustained perforin expression in DL and anti-IL-15 monoclonal antibody abrogated this effect. DAC increased cytotoxicity of DL against K-562 which was mediated by IL-15.

CONCLUSION

Interleukin-15, probably produced by DAC, upregulates cytolytic mediators' expression and perforin-mediated cytotoxicity of DL, with equal efficiency as high concentrations of IL-2.

摘要

问题

我们研究了与白细胞介素(IL)-2相比,蜕膜黏附细胞(DAC)和白细胞介素(IL)-15是否会影响孕早期蜕膜淋巴细胞(DL)的细胞溶解潜能。

研究方法

通过酶消化和密度梯度离心获得蜕膜单核细胞。非黏附性DL在黏附2小时后收集,并分别与以下物质一起培养18或72小时:IL-15(0.5 - 5 ng/mL)、IL-2(100 - 1000 U/mL)或这两种细胞因子、DAC(比例为3:1和1:1)或DAC与抗IL-15抗体。在指定培养条件下,检测穿孔素、Fas配体(FasL)和颗粒酶B的mRNA水平。通过2小时PKH-26细胞毒性试验测量DL对K-562、P815和P815-Fas的细胞溶解活性。在DL与K-562靶细胞接触后,测量穿孔素蛋白和mRNA表达的动态变化。

结果

培养18小时后,白细胞介素-15增强了穿孔素、FasL和颗粒酶B的转录,并防止了DL培养后观察到的穿孔素蛋白下调。IL-2有类似作用。DAC维持了DL中穿孔素的表达,而抗IL-15单克隆抗体消除了这种作用。DAC增加了DL对K-562的细胞毒性,这是由IL-15介导的。

结论

可能由DAC产生的白细胞介素-15上调了细胞溶解介质的表达以及DL的穿孔素介导的细胞毒性,其效率与高浓度的IL-2相同。

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