Tian Jie, Rui Ke, Tang Xinyi, Wang Wenxin, Ma Jie, Tian Xinyu, Wang Yungang, Xu Huaxi, Lu Liwei, Wang Shengjun
Department of Laboratory Medicine, The Affiliated People's Hospital, Jiangsu University, Zhenjiang, China.
Institute of Laboratory Medicine, Jiangsu Key Laboratory for Laboratory Medicine, Jiangsu University, Zhenjiang, China.
Oncotarget. 2016 Jul 12;7(28):42953-42962. doi: 10.18632/oncotarget.10261.
Olfactory ecto-mesenchymal stem cells (OE-MSCs) are a population of cells which has been recognized as a new resident stem cell type in the olfactory lamina propria. OE-MSCs have been shown to exert their immunosuppressive capacity by modulating T cell responses, including up-regulation of regulatory T cells (Tregs) and down-regulation of Th1/Th17 cells. As an inflammatory cytokine, IL-17 plays a critical role in orchestrating the inflammatory response during the development of collagen-induced arthritis (CIA). However, it is unclear whether the increased level of IL-17 may affect the immunosuppressive function of OE-MSCs under inflammatory condition. In this study, we found that IL-17 could significantly reduce the suppressive capacity of OE-MSCs on CD4+ T cells and down-regulate the suppressive factors produced by OE-MSCs. Notably, IL-17 treatment abolished the capacity of OE-MSCs in inducing Treg expansion. In addition, knockdown of IL-17R in OE-MSCs significantly enhanced their therapeutic effect in ameliorating CIA upon adoptive transfer. Moreover, IL-17R knockdown-OE-MSCs could efficiently induce Tregs expansion and reduce Th1 and Th17 responses. Taken together, all these data suggest that IL-17R knockdown in OE-MSCs may provide a novel strategy in maintaining their immunosuppressive properties for the treatment of autoimmune diseases.
嗅觉外胚层间充质干细胞(OE-MSCs)是一类已被确认为嗅黏膜固有层中新型驻留干细胞类型的细胞。OE-MSCs已被证明可通过调节T细胞反应发挥其免疫抑制能力,包括上调调节性T细胞(Tregs)和下调Th1/Th17细胞。作为一种炎性细胞因子,白细胞介素-17(IL-17)在胶原诱导的关节炎(CIA)发展过程中协调炎症反应方面发挥着关键作用。然而,尚不清楚IL-17水平升高是否会在炎症条件下影响OE-MSCs的免疫抑制功能。在本研究中,我们发现IL-17可显著降低OE-MSCs对CD4+T细胞的抑制能力,并下调OE-MSCs产生的抑制因子。值得注意的是,IL-17处理消除了OE-MSCs诱导Treg扩增的能力。此外,在OE-MSCs中敲低IL-17R可显著增强其在过继转移后改善CIA的治疗效果。而且,敲低IL-17R的OE-MSCs可有效诱导Tregs扩增并减少Th1和Th17反应。综上所述,所有这些数据表明,在OE-MSCs中敲低IL-17R可能为维持其免疫抑制特性以治疗自身免疫性疾病提供一种新策略。