Figueroa D J, Borish L, Baramki D, Philip G, Austin C P, Evans J F
Department of Neuroscience, Merck Research Laboratories, West Point, PA 19468, USA.
Clin Exp Allergy. 2003 Oct;33(10):1380-8. doi: 10.1046/j.1365-2222.2003.01786.x.
Cysteinyl leukotrienes (CysLTs) are bioactive lipids that have been shown to contribute to allergic and inflammatory diseases. Eosinophils and mast cells have the capacity to produce large amounts of CysLTs after allergic or non-allergic stimulation. Molecular identification of both the synthetic and signalling proteins in the CysLT pathway allows the investigation of expression of the CysLT enzymes and receptors in active allergic rhinitis.
We examined the expression of the proteins involved in the synthesis of CysLTs and the cysteinyl leukotriene-1 (CysLT1) and cysteinyl leukotriene-2 (CysLT2) receptors in inflammatory cells from patients with active seasonal allergic rhinitis.
Nasal lavage samples were obtained from patients during active seasonal allergic rhinitis. Specific cellular immunocytochemical techniques were used to detect the cysteinyl leukotriene synthetic proteins, namely 5-lipoxygenase (5-LO), 5-lipoxygenase-activating protein (FLAP) and leukotriene C4 synthase (LTC4S). In situ hybridization and immunocytochemical techniques were used to identify the mRNA and proteins for the CysLT1 and CysLT2 receptors.
5-LO, FLAP and LTC4S, and the CysLT1 and CysLT2 receptors were expressed in the majority of eosinophils and in subsets of mast cells and mononuclear cells. 5-LO, FLAP and the CysLT1 receptor, but not LTC4S or the CysLT2 receptor, were expressed in a subset of nasal neutrophils.
Our study demonstrates the presence of CysLT pathway proteins in key allergic and inflammatory cells from the upper airway of patients with active seasonal allergic rhinitis. Our expression data highlight the potential of CysLT-modifying agents to treat both upper and lower airway symptoms in patients suffering from allergic rhinitis and asthma.
半胱氨酰白三烯(CysLTs)是生物活性脂质,已被证明与过敏性和炎症性疾病有关。嗜酸性粒细胞和肥大细胞在过敏或非过敏刺激后能够产生大量的CysLTs。对CysLT途径中的合成蛋白和信号蛋白进行分子鉴定,有助于研究活性过敏性鼻炎中CysLT酶和受体的表达情况。
我们检测了活性季节性过敏性鼻炎患者炎症细胞中参与CysLTs合成的蛋白以及半胱氨酰白三烯1(CysLT1)和半胱氨酰白三烯2(CysLT2)受体的表达情况。
在活性季节性过敏性鼻炎期间从患者获取鼻腔灌洗样本。采用特异性细胞免疫细胞化学技术检测半胱氨酰白三烯合成蛋白,即5-脂氧合酶(5-LO)、5-脂氧合酶激活蛋白(FLAP)和白三烯C4合酶(LTC4S)。采用原位杂交和免疫细胞化学技术鉴定CysLT1和CysLT2受体的mRNA和蛋白。
5-LO、FLAP和LTC4S以及CysLT1和CysLT2受体在大多数嗜酸性粒细胞以及肥大细胞和单核细胞亚群中表达。5-LO、FLAP和CysLT1受体在一部分鼻中性粒细胞中表达,但LTC4S或CysLT2受体未表达。
我们的研究证明了活性季节性过敏性鼻炎患者上呼吸道关键的过敏和炎症细胞中存在CysLT途径蛋白。我们的表达数据突出了CysLT修饰剂治疗过敏性鼻炎和哮喘患者上下呼吸道症状的潜力。