Jablonska E
Department of Immunology, Medical Academy of Bialystok, Washington 15A, 15-274 Bialystok, Poland.
Mediators Inflamm. 2002 Oct;11(5):325-8. doi: 10.1080/09629350210000015746.
It has recently been shown that soluble interleukin-6 receptor (sIL-6R) alone or complexed with interleukin (IL)-6, besides their regulatory role in a wide variety of both normal and abnormal biologic reactions mediated by IL-6, could be an effective stimulator of the cell function.
The key question of the present study is whether the sIL-6Ralpha or sIL-6R with IL-6 released by polymorphonuclear leukocytes (PMN) can influence cytokine secretion such as tumor necrosis factor-alpha (TNF-alpha) by peripheral blood mononuclear cells (PBMC), which together with PMN develop the inflammatory and immune response of a host.
Cells were isolated from heparinized whole blood of healthy persons. The PMN were cultured for 1 h at 37 degrees C in 5% CO(2). After incubation, the culture supernatant of PMN was removed and was added to PBMC. The PBMC were cultured for 1 h at 37 degrees C in the same conditions. In the culture supernatants and lysates of PMN, we examined the concentrations of sIL-6R by enzyme-linked immunosorbent assay (ELISA). TNF-alpha was measured at both protein and mRNA levels. Protein levels were determined by ELISA. To examine TNF-alpha mRNA expression, we isolated mRNA from PBMC after culture, using TRIZOL Reagent. The quantity of mRNA TNF-alpha was determined by the Quantikine mRNA assay.
The results obtained revealed that sIL-6R with IL-6 secreted by PMN may play a regulatory role in the immune response by modulating the TNF-alpha expression and its production by PBMC. This may have a significant influence on an early phase of the inflammation and other reactions mediated by TNF-alpha.
最近研究表明,可溶性白细胞介素-6受体(sIL-6R)单独或与白细胞介素(IL)-6形成复合物时,除了在IL-6介导的多种正常和异常生物学反应中发挥调节作用外,还可能是细胞功能的有效刺激物。
本研究的关键问题是,多形核白细胞(PMN)释放的sIL-6Rα或与IL-6结合的sIL-6R是否会影响外周血单核细胞(PBMC)分泌肿瘤坏死因子-α(TNF-α)等细胞因子,PBMC与PMN共同参与宿主的炎症和免疫反应。
从健康人的肝素化全血中分离细胞。PMN在37℃、5%二氧化碳条件下培养1小时。培养后,去除PMN的培养上清液并添加到PBMC中。PBMC在相同条件下于37℃培养1小时。在PMN的培养上清液和裂解物中,我们通过酶联免疫吸附测定(ELISA)检测sIL-6R的浓度。在蛋白质和mRNA水平上测量TNF-α。蛋白质水平通过ELISA测定。为检测TNF-α mRNA表达,我们在培养后使用TRIZOL试剂从PBMC中分离mRNA。通过Quantikine mRNA测定法测定TNF-α mRNA的量。
所得结果表明,PMN分泌的与IL-6结合的sIL-6R可能通过调节PBMC中TNF-α的表达及其产生,在免疫反应中发挥调节作用。这可能对炎症早期阶段以及由TNF-α介导的其他反应产生重大影响。