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白三烯B4/白三烯B4受体1通路在变应原诱导的气道高反应性和炎症中的作用。

Role of the LTB4/BLT1 pathway in allergen-induced airway hyperresponsiveness and inflammation.

作者信息

Miyahara Nobuaki, Miyahara Satoko, Takeda Katsuyuki, Gelfand Erwin W

机构信息

Division of Cell Biology, Department of Pediatrics, National Jewish Medical and Research Center, Denver, CO 80206, USA.

出版信息

Allergol Int. 2006 Jun;55(2):91-7. doi: 10.2332/allergolint.55.91.

Abstract

LTB4, a proinflammatory lipid mediator generated from arachidonic acid through the action of 5-lipoxygenase, has been known for over two decades and is implicated in a wide variety of inflammatory disorders. BLT1, a G-protein-coupled receptor, has recently been identified as a high affinity receptor specific for LTB4. Recent studies in allergen-induced airway hyperresponsiveness and inflammation using mice lacking BLT1 have shown crucial new roles for leukotriene B4 and BLT1 in Th2 cytokine IL-13 production from lung T cells and recruitment of antigen-specific effector CD8+ T cells, suggesting novel mechanisms for their actions. The leukotriene B4-BLT1 pathway is an important target for the treatment of bronchial asthma.

摘要

白三烯B4(LTB4)是一种通过5-脂氧合酶作用由花生四烯酸生成的促炎脂质介质,二十多年来一直为人所知,并且与多种炎症性疾病有关。白三烯B4受体1(BLT1)是一种G蛋白偶联受体,最近被鉴定为对白三烯B4具有特异性的高亲和力受体。最近利用缺乏BLT1的小鼠进行的关于变应原诱导的气道高反应性和炎症的研究表明,白三烯B4和BLT1在肺T细胞产生Th2细胞因子白细胞介素-13以及抗原特异性效应性CD8 + T细胞的募集中发挥了关键的新作用,提示了它们作用的新机制。白三烯B4 - BLT1途径是治疗支气管哮喘的重要靶点。

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