白细胞介素-29增强肿瘤坏死因子-α刺激的人口腔上皮细胞中CXCL10的产生。
IL-29 Enhances CXCL10 Production in TNF-α-stimulated Human Oral Epithelial Cells.
作者信息
Hosokawa Yoshitaka, Hosokawa Ikuko, Shindo Satoru, Ozaki Kazumi, Matsuo Takashi
机构信息
a Department of Conservative Dentistry, Institute of Biomedical Sciences , Tokushima University Graduate School , Tokushima , Japan.
b Department of Oral Health Care Promotion, Institute of Biomedical Sciences , Tokushima University Graduate School , Tokushima , Japan.
出版信息
Immunol Invest. 2017 Aug;46(6):615-624. doi: 10.1080/08820139.2017.1336176.
Interleukin-29 (IL-29) is a cytokine belonging to the Type III interferon family. It was recently detected in the gingival crevicular fluid of periodontitis patients. However, the role of IL-29 in the pathogenesis of periodontal disease remains unknown. The aim of this study was to examine the effects of IL-29 on C-X-C motif chemokine ligand 10 (CXCL10) production in human oral epithelial cells. We measured CXCL10 production in TR146 cells, which is a human oral epithelial cell line, using an enzyme-linked immunosorbent assay. We used a Western blot analysis to detect IL-29 receptor expression and the phosphorylation levels of signal transduction molecules, including p38 mitogen-activated protein kinases (MAPK), signal transducer and activator of transcription 3 (STAT3), and nuclear factor (NF)- κB p65, in the TR146 cells. The TR146 cells expressed the IL-29 receptor. IL-29 induced CXCL10 production in the TR146 cells. IL-29 significantly enhanced CXCL10 production in tumor necrosis factor (TNF)-α-stimulated TR146 cells. The p38 MAPK, STAT3, and NF-κB pathways were found to be related to the IL-29-induced enhancement of CXCL10 production in TNF-α-stimulated TR146 cells. IL-29 promotes T helper 1-cell accumulation in periodontal lesions by inducing CXCL10 production in oral epithelial cells.
白细胞介素-29(IL-29)是一种属于III型干扰素家族的细胞因子。最近在牙周炎患者的龈沟液中检测到了它。然而,IL-29在牙周疾病发病机制中的作用仍然未知。本研究的目的是检测IL-29对人口腔上皮细胞中C-X-C基序趋化因子配体10(CXCL10)产生的影响。我们使用酶联免疫吸附测定法测量了人口腔上皮细胞系TR146细胞中CXCL10的产生。我们使用蛋白质印迹分析来检测TR146细胞中IL-29受体的表达以及信号转导分子的磷酸化水平,包括p38丝裂原活化蛋白激酶(MAPK)、信号转导及转录激活因子3(STAT3)和核因子(NF)-κB p65。TR146细胞表达IL-29受体。IL-29诱导TR146细胞产生CXCL10。IL-29显著增强肿瘤坏死因子(TNF)-α刺激的TR146细胞中CXCL10的产生。发现p38 MAPK、STAT3和NF-κB信号通路与IL-29诱导的TNF-α刺激的TR146细胞中CXCL10产生的增强有关。IL-29通过诱导口腔上皮细胞产生CXCL10促进牙周病变中辅助性T细胞1的积聚。