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Heparan sulfate proteoglycans in glomerular inflammation

机译:硫酸乙酰肝素蛋白聚糖在肾小球炎症中的作用

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Heparan sulfate proteoglycans in glomerular inflammation.Heparan sulfate proteoglycans (HSPGs) are glycoproteins consisting of a core protein to which linear heparan sulfate side chains are covalently attached. These heparan sulfate side chains can be modified at different positions by several enzymes, which include N-deacetylases, N- and O-sulfotransferases, and an epimerase. These heparan sulfate modifications give rise to an enormous structural diversity, which corresponds to the variety of biologic functions mediated by heparan sulfate, including its role in inflammation. The HSPGs in the glomerular basement membrane (GBM), perlecan, agrin, and collagen XVIII, play an important role in the charge-selective permeability of the glomerular filter. In addition to these HSPGs, various cell types express HSPGs at their cell surface, which include syndecans, glypicans, CD44, and betaglycan.During inflammation, HSPGs, especially heparan sulfate, in the extracellular matrix (ECM) and at the surface of endothelial cells bind chemokines, which establishes a local concentration gradient recruiting leukocytes. Endothelial and leukocyte cell surface HSPGs also play a role in their direct adhesive interactions via other cell surface adhesion molecules, such as selectins and 2 integrin. Activated leukocytes and endothelial cells exert heparanase activity, resulting in degradation of heparan sulfate moieties in the ECM, which facilitates leukocyte passage into tissues and the release of heparan sulfate–bound factors. In various renal inflammatory diseases the expression of agrin and GBM-associated heparan sulfate is decreased, while the expression of CD44 is increased. Heparan sulfate or heparin preparations affect inflammatory cell behavior and have promising therapeutic, anti-inflammatory properties by preventing leukocyte adhesion/influx and tissue damage.
机译:肾小球炎症中的硫酸乙酰肝素蛋白聚糖。硫酸乙酰肝素蛋白聚糖(HSPG)是由核心蛋白组成的糖蛋白,线性硫酸乙酰肝素侧链与之共价结合。这些硫酸乙酰肝素侧链可通过几种酶在不同位置修饰,这些酶包括N-脱乙酰基酶,N-和O-磺基转移酶和差向异构酶。这些硫酸乙酰肝素修饰产生巨大的结构多样性,其对应于由硫酸乙酰肝素介导的多种生物学功能,包括其在炎症中的作用。肾小球基底膜(GBM)中的HSPG,perlecan,凝集素和XVIII胶原蛋白在肾小球滤膜的电荷选择性渗透中起重要作用。除了这些HSPG以外,各种细胞类型还在其细胞表面表达HSPG,包括合成多糖,甘聚糖,CD44和β聚糖。在炎症过程中,HSPG特别是硫酸乙酰肝素在细胞外基质(ECM)和内皮细胞表面表达。结合趋化因子,从而建立募集白细胞的局部浓度梯度。内皮细胞和白细胞细胞表面HSPG在经由其他细胞表面粘附分子(例如选择素和2整联蛋白)的直接粘附相互作用中也起作用。激活的白细胞和内皮细胞发挥乙酰肝素酶活性,导致ECM中硫酸乙酰肝素部分降解,从而促进白细胞进入组织并释放硫酸乙酰肝素结合因子。在各种肾脏炎性疾病中,凝集素和GBM相关的硫酸乙酰肝素的表达降低,而CD44的表达增加。硫酸乙酰肝素或肝素制剂可通过防止白细胞粘附/流入和组织损伤来影响炎症细胞行为并具有有希望的治疗性抗炎特性。

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