首页> 外文期刊>Clinical and experimental allergy : >Conditioned polarized Caco-2 cell monolayers allow to discriminate for the ability of gut-derived microorganisms to modulate permeability and antigen-induced basophil degranulation.
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Conditioned polarized Caco-2 cell monolayers allow to discriminate for the ability of gut-derived microorganisms to modulate permeability and antigen-induced basophil degranulation.

机译:条件极化的Caco-2细胞单层可以区分肠源性微生物调节通透性和抗原诱导的嗜碱性粒细胞脱粒的能力。

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BACKGROUND: Food allergy is a common allergic disorder--especially in early childhood. The avoidance of the allergenic food is the only available method to prevent further reactions in sensitized patients. A better understanding of the immunologic mechanisms involved in this reaction would help to develop therapeutic approaches applicable to the prevention of food allergy. OBJECTIVE: To establish a multi-cell in vitro model of sensitized intestinal epithelium that mimics the intestinal epithelial barrier to study the capacity of probiotic microorganisms to modulate permeability, translocation and immunoreactivity of ovalbumin (OVA) used as a model antigen. METHODS: Polarized Caco-2 cell monolayers were conditioned by basolateral basophils and used to examine apical to basolateral transport of OVA by ELISA. Activation of basophils with translocated OVA was measured by beta-hexosaminidase release assay. This experimental setting was used to assess how microorganisms added apically affected these parameters. Basolateral secretion of cytokine/chemokines by polarized Caco-2 cell monolayers was analysed by ELISA. RESULTS: Basophils loaded with OVA-specific IgE responded to OVA in a dose-dependent manner. OVA transported across polarized Caco-2 cell monolayers was found to trigger basolateral basophil activation. Microorganisms including lactobacilli and Escherichia coli increased transepithelial electrical resistance while promoting OVA passage capable to trigger basophil activation. Non-inflammatory levels of IL-8 and thymic stromal lymphopoietin were produced basolaterally by Caco-2 cells exposed to microorganisms. CONCLUSION: The complex model designed in here is adequate to learn about the consequence of the interaction between microorganisms and epithelial cells vis-a-vis the barrier function and antigen translocation, two parameters essential to mucosal homeostasis. It can further serve as a direct tool to search for microorganisms with anti-allergic and anti-inflammatory properties.
机译:背景:食物过敏是一种常见的过敏性疾病,尤其是在儿童早期。避免过敏食品是防止致敏患者进一步反应的唯一可用方法。更好地了解此反应所涉及的免疫机制将有助于开发适用于预防食物过敏的治疗方法。目的:建立致敏肠上皮的多细胞体外模型,模拟肠上皮屏障,以研究益生菌调节作为模型抗原的卵清蛋白(OVA)的渗透性,易位性和免疫反应性的能力。方法:用基底外侧嗜碱细胞调节极化的Caco-2细胞单层,并通过ELISA检测OVA的顶端至基底外侧转运。通过β-己糖胺酶释放测定法测量了易位的OVA对嗜碱性粒细胞的激活。该实验设置用于评估添加的微生物如何对这些参数产生影响。通过ELISA分析极化的Caco-2细胞单层的细胞因子/趋化因子的基底外侧分泌。结果:载有OVA特异性IgE的嗜碱性粒细胞对OVA的反应呈剂量依赖性。发现跨极化Caco-2细胞单层转运的OVA触发了基底外侧嗜碱性粒细胞活化。包括乳酸菌和大肠杆菌在内的微生物增加了跨上皮的电阻,同时促进了能够触发嗜碱性粒细胞活化的OVA通道。暴露于微生物的Caco-2细胞在基底外侧产生非炎性水平的IL-8和胸腺基质淋巴细胞生成素。结论:本文设计的复杂模型足以了解微生物与上皮细胞之间相互作用对屏障功能和抗原易位性的影响,这是粘膜稳态的两个重要参数。它可以进一步用作搜索具有抗过敏和抗炎特性的微生物的直接工具。

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