Tokmadzić Vlatka S, Tsuji Yoshiyuki, Bogović Tatjana, Laskarin Gordana, Cupurdija Kristijan, Strbo Natasa, Koyama Koji, Okamura Haruki, Podack Eckhard R, Rukavina Daniel
Department of Physiology and Immunology, Medical Faculty, University of Rijeka, Rijeka, Croatia.
Am J Reprod Immunol. 2002 Oct;48(4):191-200. doi: 10.1034/j.1600-0897.2002.01132.x.
Perforin expressing uterine natural killer (uNK) cells are under complex cytokine influence. The aim of the study was to investigate the presence and role of interleukin (IL)-18 on NK cytolytic potential at maternal-fetal (M-F) interface.
Peripheral blood cells and decidual tissue were obtained from elective pregnancy termination of normal human 6-10-week-old pregnancies. Perforin expression and cytolytic activity of peripheral blood (PBL) and decidual lymphocytes (DL) were analyzed by flow cytometry. IL-18 positive decidual adherent cells (DAC) were detected by the same method. Interleukin-18 and IL-18 receptor (IL-18R) expression on the trophoblastic cells was detected by immunohistology using biotinylated anti-IL-18 and IL-18R monoclonal antibodies.
The IL-18 added in a dose of 10 ng/mL up-regulates perforin expression and cytolytic activity of DL. Simultaneous stimulation with IL-18 and IL-12 enhanced DL cytolytic activity, while IL-18 combined with IL-10 or IL-15 did not show this effect. Cytolytic activity of PBL was up-regulated by IL-18 as well, and this effect was enhanced by the addition of IL-12 and IL-15. Interleukin-18 did not affect perforin-protein expression in cultured PBL. Approximately 20% of DAC were IL-18 positive and these cells were mostly human leukocyte antigen (HLA)-DR negative. IL-18R positive cells were found on syncytiotrophoblast cell layer, interstitial tissue cells of villi and fetal blood cells. There was no detectable IL-18 staining on trophoblast cell layer on villi, but strong staining of fetal blood cells in villous vessels.
These are first results showing IL-18R expression, but not IL-18 expression on villous trophoblastic cells, as well as enhancement of perforin expression and NK cytolytic potential of DL under the influence of IL-18. IL-18 in concert with other cytokines and hormones could play an important role in the regulation of cytolytic potential of first trimester pregnancy decidual and peripheral blood NK cells.
表达穿孔素的子宫自然杀伤(uNK)细胞受到复杂的细胞因子影响。本研究的目的是调查白细胞介素(IL)-18在母胎(M-F)界面处对NK细胞溶解潜能的存在及作用。
从6-10周龄正常人类妊娠的选择性终止妊娠中获取外周血细胞和蜕膜组织。通过流式细胞术分析外周血(PBL)和蜕膜淋巴细胞(DL)的穿孔素表达和细胞溶解活性。用相同方法检测IL-18阳性的蜕膜贴壁细胞(DAC)。使用生物素化的抗IL-18和IL-18受体(IL-18R)单克隆抗体,通过免疫组织学检测滋养层细胞上的白细胞介素-18和IL-18R表达情况。
以10 ng/mL剂量添加的IL-18上调了DL的穿孔素表达和细胞溶解活性。IL-18和IL-12同时刺激增强了DL的细胞溶解活性,而IL-18与IL-10或IL-15联合使用未显示此效果。IL-18也上调了PBL的细胞溶解活性,并且添加IL-12和IL-15可增强此效果。白细胞介素-18不影响培养的PBL中穿孔素蛋白的表达。约20%的DAC为IL-18阳性,且这些细胞大多为人类白细胞抗原(HLA)-DR阴性。在合体滋养层细胞层、绒毛间质组织细胞和胎儿血细胞上发现了IL-18R阳性细胞。绒毛滋养层细胞层未检测到IL-18染色,但绒毛血管中的胎儿血细胞有强染色。
这些是首次显示绒毛滋养层细胞上有IL-18R表达但无IL-18表达,以及在IL-18影响下DL的穿孔素表达和NK细胞溶解潜能增强的结果。IL-18与其他细胞因子和激素协同作用,可能在孕早期妊娠蜕膜和外周血NK细胞溶解潜能的调节中起重要作用。