Xue Ming, Zhang Xiwen, Chen Jianxiao, Liu Feng, Xu Jingyuan, Xie Jianfeng, Yang Yi, Yu Weiping, Qiu Haibo
Department of Critical Care Medicine, Zhongda Hospital, School of Medicine, Southeast University, Nanjing 210009, China.
Department of Pathophysiology, School of Medicine, Southeast University, Nanjing 210009, China.
Stem Cells Int. 2022 Mar 12;2022:5522828. doi: 10.1155/2022/5522828. eCollection 2022.
Regulatory T cell (Treg)/T helper (Th) 17 skewing is important in the development of acute respiratory distress syndrome (ARDS). Immunomodulatory effects of mesenchymal stem cell- (MSC-) secreted transforming growth factor- (TGF-) 1 on CD4 T cells are environment-sensitive and lack discussion in hypoxic and inflammatory conditions.
Mouse splenic CD4 T cells were precoated with anti-CD3 (5 g/ml) and anti-CD28 (2 g/ml) overnight. RAW264.7 cells were added as antigen-presenting cells (APCs). T cells with and without RAW264.7 cells were treated with various LPS concentrations of 0, 10, 100, and 1000 ng/ml or/and at hypoxia condition of 5% O. Based on LPS (100 ng/ml) and hypoxia conditions (5% O) as stimuli, MSCs were set as direct coculture or indirect coculture by transwell system. Anti-TGF-1 neutralization antibody was added to explore the role of TGF-1 among the soluble factors secreted by MSCs; miR-155 overexpression of CD4 T cells was performed by transfection, and then, cells were added to the MSC-CD4 T cell coculture system in hypoxic- and LPS-stimulated condition. After 48 hours, cells or supernatants were collected for detection of frequency of Treg and Th17 subsets, CD4 T cell apoptosis and proliferation capacity assay by flow cytometry, secretion of INF-, IL-17A, IL-21, TGF-1, and IL-10 by ELISA, and levels of miR-155, Rorc, Foxp3, and Ptpn2 mRNA expression of CD4 T cells by RT-PCR.
MSCs could restore skewed Treg/Th17 induced by LPS and hypoxia compared to groups without MSCs with increased secretion of TGF-1, IL-10, and IL-17A ( < 0.05) and attenuate the increased expression of miR-155 in CD4 T cells via cell-to-cell contact mechanism while TGF-1 neutralization significantly inhibited the effects of MSCs restoring skewed Treg/Th17 and abolished its effect on miR-155 expression in CD4 T cells.
These findings suggested miR-155 suppression of CD4 T cells mediated MSC-secreted TGF-1 modulating skewed Treg/Th17 induced by LPS-hypoxia challenge, providing evidence when proposing future T lymphocyte-targeted cell therapy in a specific condition.
调节性T细胞(Treg)/辅助性T细胞(Th)17失衡在急性呼吸窘迫综合征(ARDS)的发生发展中起重要作用。间充质干细胞(MSC)分泌的转化生长因子(TGF)-1对CD4 T细胞的免疫调节作用具有环境敏感性,且在缺氧和炎症条件下缺乏相关讨论。
将小鼠脾脏CD4 T细胞用抗CD3(5μg/ml)和抗CD28(2μg/ml)预包被过夜。加入RAW264.7细胞作为抗原呈递细胞(APC)。将有或无RAW264.7细胞的T细胞用0、10、100和1000 ng/ml的不同脂多糖(LPS)浓度处理或/和在5%氧气的缺氧条件下处理。以LPS(100 ng/ml)和缺氧条件(5%氧气)作为刺激因素,将MSC设置为通过Transwell系统进行直接共培养或间接共培养。加入抗TGF-1中和抗体以探讨TGF-1在MSC分泌的可溶性因子中的作用;通过转染使CD4 T细胞过表达miR-155,然后将细胞加入缺氧和LPS刺激条件下的MSC-CD4 T细胞共培养系统。48小时后,收集细胞或上清液,通过流式细胞术检测Treg和Th17亚群的频率、CD4 T细胞凋亡和增殖能力,通过酶联免疫吸附测定(ELISA)检测INF-、IL-17A、IL-21、TGF-1和IL-10的分泌情况,通过逆转录-聚合酶链反应(RT-PCR)检测CD4 T细胞中miR-155、Rorc、Foxp3和Ptpn2 mRNA的表达水平。
与无MSC的组相比,MSC可恢复由LPS和缺氧诱导的Treg/Th17失衡,TGF-1、IL-10和IL-17A的分泌增加(P<0.05),并通过细胞间接触机制减弱CD4 T细胞中miR-155的表达增加,而TGF-1中和显著抑制MSC恢复失衡的Treg/Th17的作用,并消除其对CD4 T细胞中miR-155表达的影响。
这些发现表明miR-155抑制CD4 T细胞介导了MSC分泌的TGF-1调节由LPS-缺氧刺激诱导的失衡的Treg/Th17,为在特定条件下提出未来的T淋巴细胞靶向细胞治疗提供了证据。