Department of Environmental Immunology, UFZ-Helmholtz Centre for Environmental Research Leipzig, Leipzig, Germany.
Department for General, Visceral, and Vascular Surgery, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Clin Exp Immunol. 2020 May;200(2):199-213. doi: 10.1111/cei.13423. Epub 2020 Feb 17.
Bile acids (BAs) are produced by liver hepatocytes and were recently shown to exert functions additional to their well-known role in lipid digestion. As yet it is not known whether the mucosal-associated invariant T (MAIT) cells, which represent 10-15% of the hepatic T cell population, are affected by BAs. The focus of the present investigation was on the association of BA serum concentration with MAIT cell function and inflammatory parameters as well as on the relationship of these parameters to body weight. Blood samples from 41 normal weight and 41 overweight children of the Lifestyle Immune System Allergy (LISA) study were analyzed with respect to MAIT cell surface and activation markers [CD107a, CD137, CD69, interferon (IFN)-γ, tumor necrosis factor (TNF)-α] after Escherichia coli stimulation, mRNA expression of promyelocytic leukemia zinc finger protein (PLZF) and major histocompatibility complex class I-related gene protein (MR1), the inflammatory markers C-reactive protein (CRP), interleukin (IL)-8 and macrophage inflammatory protein (MIP)-1α as well as the concentrations of 13 conjugated and unconjugated BAs. Higher body weight was associated with reduced MAIT cell activation and expression of natural killer cell marker (NKp80) and chemokine receptor (CXCR3). BA concentrations were positively associated with the inflammatory parameters CRP, IL-8 and MIP-1α, but were negatively associated with the number of activated MAIT cells and the MAIT cell transcription factor PLZF. These relationships were exclusively found with conjugated BAs. BA-mediated inhibition of MAIT cell activation was confirmed in vitro. Thus, conjugated BAs have the capacity to modulate the balance between pro- and anti-inflammatory immune responses.
胆汁酸(BAs)由肝脏肝细胞产生,最近被证明除了在脂质消化中的作用外,还具有其他功能。目前尚不清楚黏膜相关不变 T(MAIT)细胞是否受 BAs 影响,MAIT 细胞占肝脏 T 细胞群体的 10-15%。本研究的重点是 BA 血清浓度与 MAIT 细胞功能和炎症参数的相关性,以及这些参数与体重的关系。对 Lifestyle Immune System Allergy(LISA)研究的 41 名正常体重和 41 名超重儿童的血液样本进行了分析,方法是在大肠杆菌刺激后检测 MAIT 细胞表面和激活标志物[CD107a、CD137、CD69、干扰素(IFN)-γ、肿瘤坏死因子(TNF)-α],并检测前髓细胞白血病锌指蛋白(PLZF)和主要组织相容性复合体 I 相关基因蛋白(MR1)的 mRNA 表达、炎症标志物 C 反应蛋白(CRP)、白细胞介素(IL)-8 和巨噬细胞炎症蛋白(MIP)-1α 以及 13 种结合型和非结合型 BAs 的浓度。较高的体重与 MAIT 细胞激活和自然杀伤细胞标志物(NKp80)和趋化因子受体(CXCR3)表达减少有关。BA 浓度与炎症参数 CRP、IL-8 和 MIP-1α 呈正相关,与活化 MAIT 细胞数量和 MAIT 细胞转录因子 PLZF 呈负相关。这些关系仅与结合型 BAs 有关。在体外证实了 BA 对 MAIT 细胞激活的抑制作用。因此,结合型 BAs 具有调节促炎和抗炎免疫反应之间平衡的能力。