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Siglec-8 和 Siglec-F,哮喘治疗的新靶点。

Siglec-8 and Siglec-F, the new therapeutic targets in asthma.

机构信息

Department of Immunology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Immunopharmacol Immunotoxicol. 2012 Oct;34(5):721-6. doi: 10.3109/08923973.2011.589453. Epub 2012 Feb 11.

Abstract

The recruitment of eosinophils from the circulation into the airway is a prominent feature of allergic asthma. Persistent inflammatory responses may arise from inefficient mechanisms for resolution of inflammation, including delayed apoptosis. Several studies suggest that eosinophil apoptosis is delayed in asthma. Sialic acid-binding immunoglobulin-like lectins are characterized by their sequence similarities and abilities to bind sialic acids in glycoproteins and glycolipids. Siglec-8 is uniquely expressed on eosinophils, mast cells, and basophils. Engagement of Siglec-8 on blood eosinophils results in caspase- and mitochondria-dependent apoptosis. Eosinophil apoptosis is an important therapeutic target for the development of novel anti-asthma treatments that specifically target the eosinophil.

摘要

嗜酸性粒细胞从循环中募集到气道是过敏性哮喘的一个显著特征。持续性炎症反应可能源于炎症消退的机制效率低下,包括细胞凋亡延迟。几项研究表明,哮喘患者的嗜酸性粒细胞凋亡延迟。唾液酸结合免疫球蛋白样凝集素的特征是序列相似性和结合糖蛋白和糖脂中唾液酸的能力。Siglec-8 独特地表现在嗜酸性粒细胞、肥大细胞和嗜碱性粒细胞上。Siglec-8 在血液嗜酸性粒细胞上的结合导致半胱天冬酶和线粒体依赖性细胞凋亡。嗜酸性粒细胞凋亡是开发新型靶向嗜酸性粒细胞的抗哮喘治疗方法的重要治疗靶点。

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