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Lung dendritic cells undergo maturation and polarization towards a T helper type 2-stimulating phenotype in a mouse model of asthma: Role of nerve growth factor

机译:哮喘小鼠模型中肺树突状细胞成熟并朝着T辅助2型刺激表型极化:神经生长因子的作用

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Nerve growth factor (NGF) and dendritic cells (DCs) have been hypothesized to modulate T cell responses in a mouse model of asthma. However, whether NGF plays a role in regulating the maturation and polarization of lung DCs remains unclear. In the present study, the effect of NGF inhibition on the maturation and phenotype of lung DCs was investigated in a mouse model of asthma. BALB/c mice were sensitized and challenged with ovalbumin (OVA), and subsequently received anti-NGF treatment. At 24 h following the last challenge, airway responsiveness and inflammation were examined. The concentrations of NGF, interferon (IFN)-gamma and interleukin (IL)-4 were analyzed. In addition, maturation and CD103 expression in the lung DCs were investigated. Anti-NGF treatment was found to significantly reduce airway hyperreactivity and inflammation in asthmatic mice. In addition, a subdued T helper 2 (Th2) response was observed, characterized by the downregulation of IL-4 and the upregulation of IFN-gamma. Furthermore, the expression of the DC surface molecules, CD80, CD86 and major histocompatibility complex class II, as well as the proportion of lung CD103+ DCs, decreased in the OVA-sensitized and challenged mice. The proportion of lung CD103(+) DCs also exhibited a positive correlation with the levels of plasma NGF in the mice. These results may provide an explanation for the role of NGF in amplifying the Th2 response in allergic diseases. Therefore, NGF may promote the maturation and polarization towards a Th2-stimulating phenotype of activated DCs, contributing to an amplification of the Th2 response in asthma.
机译:已经假设在哮喘的小鼠模型中神经生长因子(NGF)和树突状细胞(DC)可以调节T细胞反应。然而,尚不清楚NGF是否在调节肺DC的成熟和极化中起作用。在本研究中,在哮喘小鼠模型中研究了NGF抑制对肺DC的成熟和表型的影响。将BALB / c小鼠致敏并用卵清蛋白(OVA)攻击,然后接受抗NGF处理。最后一次挑战后24小时,检查气道反应性和炎症。分析了NGF,干扰素(IFN)-γ和白介素(IL)-4的浓度。另外,研究了肺DC中的成熟和CD103表达。发现抗NGF治疗可显着降低哮喘小鼠的气道高反应性和炎症。此外,观察到柔和的T辅助2(Th2)反应,其特征在于IL-4的下调和IFN-γ的上调。此外,在OVA致敏和攻击的小鼠中,DC表面分子,CD80,CD86和II类主要组织相容性复合物的表达以及肺CD103 + DC的比例下降。肺CD103(+)DC的比例也与小鼠血浆NGF的含量呈正相关。这些结果可能为NGF在变应性疾病中放大Th2反应中的作用提供了解释。因此,NGF可能促进成熟DC和向激活的DC的Th2刺激表型极化,从而导致哮喘中Th2反应的扩增。

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