College of Food Science and Technology, Yunnan Agricultural University, Kunming 650201, China.
Yunnan Key Laboratory of Precision Nutrition and Personalized Food Manufacturing, Yunnan Agricultural University, Kunming 650201, China.
Nutrients. 2023 Dec 19;16(1):7. doi: 10.3390/nu16010007.
leaves are an inexpensive substitute for staple foods. Despite limited data, leaf protein (Mo-Pr) may be allergenic in BALB/c mice. In mouse models and allergic patients, dendritic cells (DCs) may be involved in food allergy. In addition, some allergens, including food allergens, can directly activate DCs and induce Th2 polarization. We investigated whether Mo-Pr can modulate the functional profile of murine bone marrow-derived dendritic cells (BMDCs) in vitro. BMDCs were obtained from mouse bone marrow cultured with granulocyte-macrophage colony-stimulating factor (GM-CSF) for 7 days and then treated with lipopolysaccharide (LPS) or Mo-Pr. BMDC phenotypes were evaluated via flow cytometry, cytokine production was assessed using ELISA, the expression of key genes was studied using qRT-PCR, the effects on T-cell differentiation were investigated using mixed lymphocyte reaction (MLR), and transcriptional changes in BMDCs were investigated using RNA-Seq. Mo-Pr-specific IgE was investigated in recipient serum after BMDC transfer. Mo-Pr treatment significantly induced BMDC maturation, increased the expression of CD80/86 and MHC II, resulted in the production of IL-12 and TNF-α, and induced T-cell differentiation. Mo-Pr treatment stimulated BMDCs' expression of the Th2 promoters OX40L and TIM-4, induced the production of the Th2-type chemokines CCL22 and CCL17, and decreased the Th1/Th2 ratio in vitro. Healthy recipients of Mo-Pr-treated BMDCs produced Mo-Pr-specific IgE.
叶子是主食的廉价替代品。尽管数据有限,但叶蛋白(Mo-Pr)在 BALB/c 小鼠中可能具有致敏性。在小鼠模型和过敏患者中,树突状细胞(DC)可能参与食物过敏。此外,一些过敏原,包括食物过敏原,可直接激活 DC 并诱导 Th2 极化。我们研究了 Mo-Pr 是否可以在体外调节小鼠骨髓来源的树突状细胞(BMDC)的功能特征。BMDC 是从小鼠骨髓中获得的,这些骨髓在粒细胞-巨噬细胞集落刺激因子(GM-CSF)培养 7 天后,然后用脂多糖(LPS)或 Mo-Pr 处理。通过流式细胞术评估 BMDC 表型,使用 ELISA 评估细胞因子产生,使用 qRT-PCR 研究关键基因的表达,使用混合淋巴细胞反应(MLR)研究对 T 细胞分化的影响,使用 RNA-Seq 研究 BMDC 中的转录变化。在 BMDC 转移后,研究了受体血清中的 Mo-Pr 特异性 IgE。Mo-Pr 处理显著诱导 BMDC 成熟,增加 CD80/86 和 MHC II 的表达,导致 IL-12 和 TNF-α的产生,并诱导 T 细胞分化。Mo-Pr 处理刺激 BMDC 表达 Th2 启动子 OX40L 和 TIM-4,诱导 Th2 型趋化因子 CCL22 和 CCL17 的产生,并降低体外 Th1/Th2 比值。接受 Mo-Pr 处理的 BMDC 的健康受体产生 Mo-Pr 特异性 IgE。