Soluble urokinase-type plasminogen activator receptor (suPAR) in multiple respiratory diseases

Ü. Can
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引用次数: 1

Abstract

Serum soluble urokinase-type plasminogen activator receptor (suPAR) is a glycoprotein secreted during infections and inflammation [1]. Urokinase-type plasminogen activator (uPA) is secreted by polymorphonuclear neutrophils (PMN) and macrophages; then uPA binds to membrane urokinase-type plasminogen activator receptor (uPAR) [2]. suPAR is formed by cleaved from the uPAR [2]. suPAR is expressed in various cell types, such as macrophages monocytes, endothelial cells and neutrophils [3]. suPAR can be potentially cause or modulate various diseases in patients with cancer, various infectious and inflammatory diseases (including infections with human immunodeficiency virus (HIV), tuberculosis, liver fibrosis and inflammatory bowel disease) [2, 3]. suPAR can convert plasminogen to plasmin, which degrades fibrin, activates matrix metalloproteases and mediates proteolysis of extracellular matrix proteins during cellular invasion [4]. suPAR modulate the functions of integrins (including activating intracellular signals, monocyte chemotaxis, cell adhesion and proliferation) [4, 5]. So suPAR contributes to cell adhesion, migration, proliferation inflammation, chemotaxis, proteolysis, immune system activation, tissue remodeling and signal transduction [5, 6]. Several studies have identified that suPAR level is a important marker in patients with various diseases and associated with a poorer outcome in a range of non-infectious and infectious diseases [2]. Biomarkers of lung disease are required to aid diagnosis, define clinical phenotypes and monitor the response to existing and new therapeutic strategies. Our review aims to explore the potential of suPAR as a general marker in the diagnosis, prognosis and follow-up of therapy of lung disease.
可溶性尿激酶型纤溶酶原激活物受体(suPAR)在多种呼吸系统疾病中的作用
血清可溶性尿激酶型纤溶酶原激活物受体(suPAR)是感染和炎症时分泌的一种糖蛋白[1]。尿激酶型纤溶酶原激活物(uPA)由多形核中性粒细胞(PMN)和巨噬细胞分泌;然后uPA结合膜尿激酶型纤溶酶原激活物受体(uPAR)[2]。suPAR是由uPAR裂解而成的[2]。suPAR在各种细胞类型中表达,如巨噬细胞、单核细胞、内皮细胞和中性粒细胞[3]。在癌症、各种感染性和炎症性疾病(包括人类免疫缺陷病毒(HIV)感染、结核病、肝纤维化和炎症性肠病)患者中,suPAR可能潜在地引起或调节各种疾病[2,3]。suPAR可将纤溶酶原转化为纤溶酶,在细胞侵袭过程中降解纤维蛋白,激活基质金属蛋白酶,介导细胞外基质蛋白的蛋白水解[4]。suPAR调节整合素的功能(包括激活细胞内信号、单核细胞趋化、细胞粘附和增殖)[4,5]。因此,suPAR参与细胞粘附、迁移、增殖炎症、趋化、蛋白水解、免疫系统激活、组织重塑和信号转导[5,6]。多项研究发现,suPAR水平是多种疾病患者的重要标志物,与一系列非传染性和传染性疾病的预后较差相关[2]。需要肺部疾病的生物标志物来帮助诊断,确定临床表型并监测对现有和新的治疗策略的反应。本综述旨在探讨suPAR作为肺部疾病诊断、预后和随访治疗的通用标志物的潜力。
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