首页> 美国卫生研究院文献>Molecules >Piperine Ameliorates Trimellitic Anhydride-Induced Atopic Dermatitis-Like Symptoms by Suppressing Th2-Mediated Immune Responses via Inhibition of STAT6 Phosphorylation
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Piperine Ameliorates Trimellitic Anhydride-Induced Atopic Dermatitis-Like Symptoms by Suppressing Th2-Mediated Immune Responses via Inhibition of STAT6 Phosphorylation

机译:哌啶通过抑制STAT6磷酸化抑制TH2介导的免疫应答来改善偏苯二酸酐诱导的特应性皮炎状症状

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摘要

Atopic dermatitis (AD) is a common inflammatory skin disease predominately related to Type 2 helper T (Th2) immune responses. In this study, we investigated whether piperine is able to improve AD symptoms using a trimellitic anhydride (TMA)-induced AD-like mouse model. Topical treatment with piperine reduced ear swelling (ear thickness and epidermal thickness) induced by TMA exposure. Furthermore, piperine inhibited pro-inflammatory cytokines such as TNF-α and IL-1β in mouse ears, compared with the TMA-induced AD group. In measuring allergic immune responses in draining lymph nodes (dLNs), we found that IL-4 secretion, GATA3 mRNA level, and STAT6 phosphorylation were suppressed by piperine treatment. In an ex vivo study, piperine also inhibited the phosphorylation of STAT6 on the CD4+ T cells isolated from splenocytes of BALB/c mice, and piperine suppressed IL-4-induced CCL26 mRNA expression and STAT6 phosphorylation in human keratinocytes resulting in the inhibition of infiltration of CCR3+ cells into inflammatory lesions. These results demonstrate that piperine could ameliorate AD symptoms through suppression of Th2-mediated immune responses, including the STAT6/GATA3/IL-4 signaling pathway. Therefore, we suggest that piperine is an excellent candidate as an inhibitor of STAT6 and may help to improve AD symptoms.
机译:特应性皮炎(AD)是一种常见的炎症性皮肤病,其主要与2型辅助T(TH2)免疫反应相关。在这项研究中,我们研究了哌啶是否能够使用偏苯二酸酐(TMA)诱导的Ad样小鼠模型来改善AD症状。用TMA暴露引起的哌啶降低耳肿胀(耳厚度和表皮厚度)的局部处理。此外,与TMA诱导的广告组相比,哌啶抑制了小鼠耳中的促炎细胞因子如小鼠耳中的TNF-α和IL-1β。在测量淋巴结(DLNS)中的过敏免疫应答时,我们发现IL-4分泌,GATA3 mRNA水平和STAT6磷酸化被哌啶处理抑制。在前体内研究中,哌啶还抑制了从BALB / C小鼠的脾细胞分离的CD4 + T细胞上的STAT6的磷酸化,哌啶抑制了人角蛋白细胞中的IL-4诱导的CCL26 mRNA表达和STAT6磷酸化导致浸润抑制CCR3 +细胞进入炎症病变。这些结果表明,哌啶可以通过抑制Th2介导的免疫应答来改善AD症状,包括STAT6 / GATA3 / IL-4信号传导途径。因此,我们建议哌啶是作为Stat6抑制剂的优秀候选者,并且可能有助于改善AD症状。

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