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炎症诱导的警报素白细胞介素33的表达可被低聚半乳糖抑制。

Inflammation-induced expression of the alarmin interleukin 33 can be suppressed by galacto-oligosaccharides.

作者信息

Verheijden Kim A T, Akbari Peyman, Willemsen Linette E M, Kraneveld Aletta D, Folkerts Gert, Garssen Johan, Fink-Gremmels Johanna, Braber Saskia

机构信息

Division of Veterinary Pharmacy, Pharmacology and Toxicology, Utrecht University, Utrecht, The Netherlands.

出版信息

Int Arch Allergy Immunol. 2015;167(2):127-36. doi: 10.1159/000437327. Epub 2015 Aug 18.

Abstract

BACKGROUND

The alarmin interleukin 33 (IL-33) and its receptor ST2 play an important role in mucosal barrier tissues, and seem to be crucial for Th2-cell mediated host defense. Galacto-oligosaccharides (GOS), used in infant formulas, exhibit gut and immune modulatory effects. To enhance our understanding of the immunomodulatory capacity of GOS, this study investigated the impact of dietary GOS intervention on IL-33 and ST2 expression related to intestinal barrier dysfunction and asthma.

METHODS

B6C3F1 and BALB/c mice were fed a control diet with or without 1% GOS. To simulate intestinal barrier dysfunction, B6C3F1 mice received a gavage with the mycotoxin deoxynivalenol (DON). To mimic asthma-like inflammatory airway responses, BALB/c mice were sensitized on day 0 and challenged on days 7-11 with house-dust mite (HDM) allergen. Samples from the intestines and lungs were collected for IL-33 and ST2 analysis by qRT-PCR, immunoblotting and immunohistochemistry.

RESULTS

Dietary GOS counteracted the DON-induced IL-33 mRNA expression and changed the IL-33 distribution pattern in the mouse small intestine. The IL-33 mRNA expression was positively correlated to the intestinal permeability. A strong positive correlation was also observed between IL-33 mRNA expression in the lung and the number of bronchoalveolar fluid cells. Reduced levels of IL-33 protein, altered IL-33 distribution and reduced ST2 mRNA expression were observed in the lungs of HDM-allergic mice after GOS intervention.

CONCLUSIONS

Dietary GOS mitigated IL-33 at the mucosal surfaces in a murine model for intestinal barrier dysfunction and HDM-induced asthma. This promising effect may open up new avenues to use GOS not only as a prebiotic in infant nutrition, but also as a functional ingredient that targets inflammatory processes and allergies associated with IL-33 expression.

摘要

背景

警报素白细胞介素33(IL-33)及其受体ST2在黏膜屏障组织中发挥重要作用,似乎对Th2细胞介导的宿主防御至关重要。用于婴儿配方奶粉的低聚半乳糖(GOS)具有肠道和免疫调节作用。为了加深我们对GOS免疫调节能力的理解,本研究调查了饮食中GOS干预对与肠道屏障功能障碍和哮喘相关的IL-33和ST2表达的影响。

方法

给B6C3F1和BALB/c小鼠喂食含或不含1%GOS的对照饮食。为模拟肠道屏障功能障碍,给B6C3F1小鼠灌胃霉菌毒素脱氧雪腐镰刀菌烯醇(DON)。为模拟哮喘样炎症气道反应,在第0天对BALB/c小鼠进行致敏,并在第7 - 11天用屋尘螨(HDM)过敏原进行激发。收集肠道和肺组织样本,通过qRT-PCR、免疫印迹和免疫组织化学分析IL-33和ST2。

结果

饮食中的GOS抵消了DON诱导的IL-33 mRNA表达,并改变了小鼠小肠中IL-33的分布模式。IL-33 mRNA表达与肠道通透性呈正相关。在肺中IL-33 mRNA表达与支气管肺泡灌洗细胞数量之间也观察到强正相关。GOS干预后,在HDM过敏小鼠的肺中观察到IL-33蛋白水平降低、IL-33分布改变以及ST2 mRNA表达降低。

结论

在肠道屏障功能障碍和HDM诱导的哮喘小鼠模型中,饮食中的GOS减轻了黏膜表面的IL-33。这种有前景的作用可能开辟新途径,使GOS不仅可作为婴儿营养中的益生元,还可作为针对与IL-33表达相关的炎症过程和过敏的功能性成分。

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