体外研究了间充质基质细胞通过体液介质特异性增强小鼠口腔鳞状细胞癌Sq-1979细胞对脾细胞干扰素γ生成能力的抑制作用

T. Inagaki, M. Mizuno-Kamiya, E. Takayama, Harumi Kawaki, E. Chihara, Y. Muramatsu, S. Sumitomo, N. Kondoh
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引用次数: 3

摘要

目的:本研究的目的是比较原发性和晚期表型的小鼠口腔鳞状细胞癌(OSCC)细胞在肿瘤环境中的免疫调节作用。我们建立了小鼠OSCC细胞、脾细胞和间充质基质细胞体外共培养体系。方法:取自C3H小鼠的OSCC细胞系Sq-1979;从Sq-1979原发肿瘤中建立了233-11个细胞;从淋巴结转移的Sq-1979细胞中建立L3-5、L5-11和L6-8细胞。10T1/2是来源于C3H小鼠的成纤维细胞系。将OSCC细胞与抗cd3抗体刺激的小鼠脾细胞共培养,在10T1/2细胞存在或不存在的情况下,采用酶联免疫吸附法评估干扰素(IFN)-γ和白细胞介素(IL)-10的产生能力。结果:在共培养l细胞存在的情况下,受刺激的脾细胞产生IFN-γ特异性增强。与所有使用的OSCC细胞系共培养时,IL-10的产生反过来减少。与直接接触的10T1/2细胞共培养时,IFN-γ的产生明显减少,在Sq-1979和233-11细胞存在时,IFN-γ的产生进一步减少,但在l细胞存在时保持不变。通过添加Sq-1979-1细胞的条件培养基也观察到IFN-γ产生的减少。结论:Sq-1979细胞通过体液因子特异性增强间充质间质细胞的免疫抑制活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Suppressive effect of mesenchymal stromal cells on interferon-γ-producing capability of spleen cells was specifically enhanced through humoral mediator(s) from mouse oral squamous cell carcinoma Sq-1979 Cells In Vitro
Aim: The aim of this study was to compare the immunomodulatory effects in the tumor milieu of mouse oral squamous cell carcinoma (OSCC) cells harboring primary and advanced phenotypes. We established an in vitro co-culture system using mouse OSCC cells, spleen cells, and mesenchymal stromal cells. Methods: Sq-1979 is an OSCC cell line derived from C3H mice; 233-11 cells were established from a primary Sq-1979 tumor; L3–5, L5–11, and L6–8 cells were established from lymph node-metastasized Sq-1979 cells. 10T1/2 is a fibroblast line derived from C3H mice. The OSCC cells were co-cultured with anti-CD3 antibody-stimulated mouse spleen cells in the presence or absence of 10T1/2 cells, and the producing capability of interferon (IFN)-γ and interleukin (IL)-10 was evaluated using enzyme-linked immunosorbent assay. Results: The production of IFN-γ by the stimulated spleen cells was specifically enhanced in the presence of co-cultured L-cells. The production of IL-10 was conversely reduced in the co-culture with all the OSCC cell lines used. The production of IFN-γ was significantly reduced in the co-culture with directly contacted 10T1/2 cells, and further reduction was observed in the presence of Sq-1979 and 233-11 cells but remained unchanged in the presence of L-cells. The reduction of IFN-γ production was also observed by the addition of conditioned medium from the Sq-1979-1 cells. Conclusion: Sq-1979 cells specifically enhanced the immune-suppressive activity of mesenchymal stromal cells through humoral factor (s).
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