IL-31 does not induce normal human ciliated epithelial cells to differentiate into a phenotype consistent with the pathophysiology of asthma

Results in immunology Pub Date : 2012-01-01 Epub Date: 2012-05-15 DOI:10.1016/j.rinim.2012.05.001
Jeremy C. Parker , Surendran Thavagnanam , Grzegorz Skibinski , Michael McBrien , Liam G. Heaney , Michael D. Shields
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引用次数: 7

Abstract

Background

IL-31 is a novel cytokine that has been implicated in allergic diseases such as atopic dermatitis and more recently asthma. While IL-31 has been well studied in skin conditions such as atopic dermatitis, little is known about the role IL-31 plays in asthma and specifically the differentiation process of the bronchial epithelium, which is central to the pathogenesis of allergic asthma.

Methods

We examined the effects of IL-13 (20 ng/ml), IL-31 (20 ng/ml) and an IL-13/IL-31 combination stimulation (20 ng/ml each) on the in vitro mucociliary differentiation of paediatric bronchial epithelial cells (PBECs) from healthy patients (n=6). IL-31 receptor (IL-31-RA) expression, markers of differentiation (goblet and ciliated cells), transepithelial electrical resistance (TEER), quantification of goblet and ciliated cells, real time PCR for MUC5AC, ELISA for VEGF, EGF and MCP-1 (CCL-2) and ELISA for MUC5AC were assessed.

Results

We found that well-differentiated PBECs expressed IL-31-RA however it's expression did not increase upon stimulation with IL-31 or either of the other treatments. TEER indicated good formation of tight junctions which was found to be similar across all treatment groups (p=0.9). We found that IL-13 alone significantly reduced the number of ciliated cells compared with unstimulated (IL-13 stimuation: mean=4.8% (SD=2.5); unstimulated: mean=15.9%, (SD=7.4), p<0.01). IL-31 stimulation alone had no effect on ciliated cells whereas the IL-13/IL-31 combination stimulation significantly reduced the number of ciliated cells compared with control (IL-13/IL-31 combination: mean=5.1% (SD=4.6); unstimulated: mean=15.9%, (SD=7.4), p<0.01). We did not find that the combination of IL-13 and IL-31 had any additional effects to that of IL-13 alone. MUC5AC mRNA and secreted mucin was found in similar levels between unstimulated and all treatments, however IL-13 increased levels of MUC5AC mRNA by a factor of 2.84, albeit not significantly, compared with unstimulated cultures (IL-13 stimulation: mean=2.84 (SD=3.79); unstimulated: mean=1.0).

Conclusions

IL-31RA receptor is present on well-differentiated paediatric bronchial epithelial cells. IL-31 does not exhibit any detrimental effects on mucociliary differentiation. IL-31 does not appear to have a synergistic effect when combined in culture with IL-13, in the differentiation process.

IL-31不能诱导正常人纤毛上皮细胞分化为符合哮喘病理生理的表型
il -31是一种新的细胞因子,与过敏性疾病如特应性皮炎和最近的哮喘有关。虽然IL-31在皮肤疾病(如特应性皮炎)中的作用已经得到了很好的研究,但对IL-31在哮喘中的作用知之甚少,特别是支气管上皮的分化过程,这是过敏性哮喘发病机制的核心。方法观察IL-13 (20 ng/ml)、IL-31 (20 ng/ml)和IL-13/IL-31联合刺激(各20 ng/ml)对健康儿童支气管上皮细胞(PBECs)体外粘膜纤毛分化的影响。评估IL-31受体(IL-31- ra)表达、分化标志物(杯状细胞和纤毛细胞)、经皮电阻(TEER)、杯状细胞和纤毛细胞定量、MUC5AC实时PCR、VEGF、EGF和MCP-1 (CCL-2) ELISA和MUC5AC ELISA。结果我们发现分化良好的PBECs表达IL-31- ra,但IL-31或其他两种处理均未增加其表达。TEER显示良好的紧密连接形成,在所有治疗组中发现相似(p=0.9)。我们发现,与未刺激相比,单独IL-13可显著减少纤毛细胞的数量(IL-13刺激:平均值=4.8% (SD=2.5);未刺激:平均值=15.9%,(SD=7.4), p<0.01)。单独刺激IL-31对纤毛细胞没有影响,而IL-13/IL-31联合刺激与对照组相比显著减少纤毛细胞数量(IL-13/IL-31联合刺激:平均值=5.1% (SD=4.6);未刺激:平均值=15.9%,(SD=7.4), p<0.01)。我们没有发现IL-13和IL-31联合使用对单独使用IL-13有任何额外的影响。未刺激和所有处理之间MUC5AC mRNA和分泌的粘蛋白水平相似,但与未刺激的培养相比,IL-13使MUC5AC mRNA水平增加了2.84倍,尽管不显著(IL-13刺激:平均值=2.84 (SD=3.79);如果:是指= 1.0)。结论sil - 31ra受体存在于分化良好的小儿支气管上皮细胞中。IL-31对纤毛粘膜分化无不良影响。在分化过程中,IL-31与IL-13联合培养时,似乎没有协同作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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