Gojoubori Takahiro, Ota Hirotaka, Kusunoki Masafumi, Nishio Yukina, Nishio Kensuke, Iwasa Satoko, Kaneko Yasuhide, Asano Masatake
a Department of Pathobiology , Nihon University School of Dentistry , Tokyo , Japan .
b Division of Immunology and Pathobiology , Nihon University School of Dentistry , Tokyo , Japan .
J Recept Signal Transduct Res. 2016;36(3):248-53. doi: 10.3109/10799893.2015.1086883. Epub 2015 Oct 19.
Human β-defensin 2 (hBD2) gene expression is dependent on nuclear factor kappa B (NF-κB) activity. We have previously demonstrated that electrolytically generated acid functional water (FW) induces the expression of hBD2 in the human oral squamous cell carcinoma (OSCC) cell line Ca9-22. However, the induction was not dependent on NF-κB activity; in fact, FW inhibited NF-κB activity. Therefore, we hypothesized that FW might reduce spontaneous interleukin 8 (IL-8) secretion by Ca9-22 cells, which is heavily dependent on NF-κB activity. This study aimed at demonstrating the inhibitory effect of FW on NF-κB activity.
Ca9-22 cells were incubated with FW, and spontaneous IL-8 secretion was observed by enzyme-linked immunosorbent assay. Luciferase assay was performed using the 5'-untranslated region of the IL-8 gene. The steps of NF-κB activation blocked by FW were evaluated by localization of the NF-κB subunits p65 and p50 by immunofluorescence staining. Western blotting was further performed to confirm the changes in NF-κB subunit localization.
The Ca9-22 cells spontaneously secreted IL-8, which was rapidly and drastically inhibited by FW treatment. The luciferase assay demonstrated the inhibitory action of FW, which was diminished by deletion of the NF-κB binding site from this construct. FW treatment altered the distribution of both the p65 and p50 subunits. P65, which was localized in the nucleus during the resting state, moved to the cytoplasm after FW treatment, whereas, p50, localized in the cytoplasm during the resting state, moved to the nucleus subsequent to FW treatment.
The results from this study indicate that FW might inhibit spontaneous IL-8 secretion by redistribution of the NF-κB subunits within the cells.
人β-防御素2(hBD2)基因表达依赖于核因子κB(NF-κB)活性。我们之前已证明,电解产生的酸性功能水(FW)可诱导人口腔鳞状细胞癌(OSCC)细胞系Ca9-22中hBD2的表达。然而,这种诱导并不依赖于NF-κB活性;事实上,FW抑制了NF-κB活性。因此,我们推测FW可能会减少Ca9-22细胞自发分泌的白细胞介素8(IL-8),而IL-8的分泌严重依赖于NF-κB活性。本研究旨在证明FW对NF-κB活性的抑制作用。
将Ca9-22细胞与FW孵育,通过酶联免疫吸附测定法观察自发IL-8分泌情况。使用IL-8基因的5'-非翻译区进行荧光素酶测定。通过免疫荧光染色对NF-κB亚基p65和p50进行定位,评估FW阻断NF-κB激活的步骤。进一步进行蛋白质印迹法以确认NF-κB亚基定位的变化。
Ca9-22细胞自发分泌IL-8,FW处理可迅速且显著抑制其分泌。荧光素酶测定证明了FW的抑制作用,从该构建体中删除NF-κB结合位点后,这种抑制作用减弱。FW处理改变了p65和p50亚基的分布。静止状态下位于细胞核中的p65在FW处理后转移至细胞质,而静止状态下位于细胞质中的p50在FW处理后转移至细胞核。
本研究结果表明,FW可能通过细胞内NF-κB亚基的重新分布来抑制自发IL-8分泌。