首页> 外文期刊>Clinical immunology: The official journal of the Clinical Immunology Society >Leukotriene D(4) enhances the function of endothelin-1-primed fibroblasts.
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Leukotriene D(4) enhances the function of endothelin-1-primed fibroblasts.

机译:白三烯D(4)增强了内皮素1启动的成纤维细胞的功能。

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摘要

Airway inflammation is accompanied by structural changes, termed remodeling, that lead to lung dysfunction over the long term. Although both endothelin-1 (ET-1) and cysteinyl leukotrienes (CysLTs) appear to be involved in airway remodeling in several lung diseases, how these molecules interact remains largely unknown. In this study, we examined the effects of leukotriene (LT) D(4) on the function of ET-1-primed fibroblasts. ET-1 at 10(-7) M up-regulated the expression of the CysLT receptors at both the mRNA and protein levels in human lung fibroblasts. LTD(4) enhanced matrix metalloproteinase-2 and pro-collagen production, and alpha-smooth muscle actin expression of ET-1-primed fibroblasts, but had little or no effect on unprimed fibroblasts. The CysLT1 receptor antagonist montelukast completely abrogated the effects of LTD(4). Our data suggested that LTD(4) may act as a precipitating factor during ET-1-mediated airway remodeling and that CysLT1 receptor antagonists may have a role in preventing aberrant extracellular matrix degradation.
机译:气道炎症伴随着结构改变,称为重塑,长期导致肺功能障碍。尽管内皮素-1(ET-1)和半胱氨酰白三烯(CysLTs)似乎都参与了几种肺部疾病的气道重塑,但这些分子如何相互作用仍然未知。在这项研究中,我们检查了白三烯(LT)D(4)对ET-1启动的成纤维细胞功能的影响。在10(-7)M处的ET-1在人肺成纤维细胞的mRNA和蛋白水平上均上调了CysLT受体的表达。 LTD(4)增强了基质金属蛋白酶2和促胶原蛋白的产生,以及ET-1启动的成纤维细胞的α平滑肌肌动蛋白表达,但对未启动的成纤维细胞几乎没有影响。 CysLT1受体拮抗剂孟鲁司特完全废除了LTD(4)的作用。我们的数据表明LTD(4)可能在ET-1介导的气道重塑过程中充当沉淀因子,而CysLT1受体拮抗剂可能在防止异常的细胞外基质降解中起作用。

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