Asgari Fatemeh, Nikzamir Abdolrahim, Baghaei Kaveh, Masotti Andrea, Rostami-Nejad Mohammad
Student Research Committee, Department of Clinical Biochemistry, School of Medicine, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Gastroenterology and Liver Diseases Research Center, Research Institute for Gastroenterology and Liver Diseases, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
Naunyn Schmiedebergs Arch Pharmacol. 2025 Apr 3. doi: 10.1007/s00210-025-04089-9.
Dendritic cells (DCs) play a crucial role in gliadin-induced inflammation in celiac disease as they are the first immune cells to encounter gliadin. Tryptophan (Trp) and vitamin A (retinol, Ret) are known to influence the immune response of DCs to gliadin and increase their tolerogenicity. CD4 + CD25 + Foxp3 + regulatory T cells (Tregs), which are important for immune tolerance, can be generated from naive T cells in the presence of retinoic acid (RA) and TGF-β.The aim of this study was to determine the combined effect of Ret and Trp in altering the phenotypic and functional maturation of DCs by gliadin and their contribution to the differentiation of Tregs. Monocyte cells derived from the peripheral blood mononuclear cells (PBMCs) of patients with celiac disease were differentiated into DCs and stimulated with PT-gliadin. These cells were then treated with Trp + Ret. The expression of CD11c, CD14, CD83, CD86, PDL1, CD4, CD25 and FOXP3 was examined using flow cytometry. TGF-β, IL-10, IL-12, and TNF-α levels were measured by ELISA. qRT-PCR was used to quantify the mRNA levels of retinaldehyde dehydrogenase 2 (RALDH2), integrin αE (CD103), and NF-κB. Indoleamine 2,3-dioxygenase (IDO) mRNA and protein levels were assessed using qRT-PCR and Western blot assays, respectively. The maturation of DCs by PT-gliadin was defined through co-stimulatory molecule expression (CD83 and CD86) and promotion of TNF-α and IL-12 secretion. We found that after treatment with Ret + Trp, the production levels of IL-12, TNF-α, and NF-κB were significantly reduced, while the expression of IL-10, TGF-β, and the inhibitory markers PDL1, CD103, IDO, and RALDH2 by PT-gliadin-stimulated DCs was significantly increased. Furthermore, in a DC and T cell co-culture system, treatment of DCs with Ret + Trp increased TGF-β expression in DCS and promoted CD4 + CD25 + FOXP3 Treg induction. These results indicate the potential benefit of vitamin A and tryptophan as therapeutic options for individuals with celiac disease. Further research is required to fully understand the mechanisms of action of these substances in these cells.
树突状细胞(DCs)在乳糜泻中麦醇溶蛋白诱导的炎症反应中起关键作用,因为它们是最早接触麦醇溶蛋白的免疫细胞。已知色氨酸(Trp)和维生素A(视黄醇,Ret)会影响DCs对麦醇溶蛋白的免疫反应并增加其耐受性。对免疫耐受很重要的CD4+CD25+Foxp3+调节性T细胞(Tregs)可在视黄酸(RA)和转化生长因子-β(TGF-β)存在的情况下由初始T细胞产生。本研究的目的是确定Ret和Trp在改变麦醇溶蛋白诱导的DCs表型和功能成熟方面的联合作用及其对Tregs分化的贡献。从乳糜泻患者外周血单个核细胞(PBMCs)中分离出的单核细胞分化为DCs,并用PT-麦醇溶蛋白刺激。然后用Trp+Ret处理这些细胞。使用流式细胞术检测CD11c、CD14、CD83、CD86、PDL1、CD4、CD25和FOXP3的表达。通过ELISA检测TGF-β、IL-10、IL-12和TNF-α水平。使用qRT-PCR定量视黄醛脱氢酶2(RALDH2)、整合素αE(CD103)和核因子κB(NF-κB)的mRNA水平。分别使用qRT-PCR和蛋白质免疫印迹法评估吲哚胺2,3-双加氧酶(IDO)的mRNA和蛋白质水平。通过共刺激分子表达(CD83和CD86)以及TNF-α和IL-12分泌的促进作用来定义PT-麦醇溶蛋白诱导的DCs成熟。我们发现,用Ret+Trp处理后,IL-12、TNF-α和NF-κB的产生水平显著降低,而PT-麦醇溶蛋白刺激的DCs中IL-10、TGF-β以及抑制性标志物PDL1、CD103、IDO和RALDH2的表达显著增加。此外,在DC和T细胞共培养系统中,用Ret+Trp处理DCs可增加DCs中TGF-β的表达并促进CD4+CD25+FOXP3 Treg的诱导。这些结果表明维生素A和色氨酸作为乳糜泻患者治疗选择的潜在益处。需要进一步研究以充分了解这些物质在这些细胞中的作用机制。