The Role of Heparan Sulfate in Inflammation, and the Development of Biomimetics as Anti-Inflammatory Strategies

被引:73
作者
Farrugia, Brooke L. [1 ]
Lord, Megan S. [1 ]
Melrose, James [1 ,2 ,3 ]
Whitelock, John M. [1 ]
机构
[1] Univ New South Wales Sydney, Grad Sch Biomed Engn, Sydney, NSW 2052, Australia
[2] Northern Sydney Local Hlth Dist, Kolling Inst, Raymond Purves Bone & Joint Res Lab, St Leonards, NSW, Australia
[3] Univ Sydney, Royal North Shore Hosp, Sydney Med Sch Northern, St Leonards, NSW, Australia
基金
澳大利亚研究理事会;
关键词
extracellular matrix; glycosaminoglycans; heparan sulfate; heparin; inflammation; innate immunity; MONOCYTE CHEMOATTRACTANT PROTEIN-1; CHEMOKINE-GLYCOSAMINOGLYCAN INTERACTIONS; SUBENDOTHELIAL EXTRACELLULAR-MATRIX; FIBROBLAST-GROWTH-FACTOR; ACTIVITY IN-VITRO; L-SELECTIN; ENDOTHELIAL-CELLS; P-SELECTIN; DIABETIC-NEPHROPATHY; BASEMENT-MEMBRANE;
D O I
10.1369/0022155417740881
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Key events that occur during inflammation include the recruitment, adhesion, and transmigration of leukocytes from the circulation to the site of inflammation. These events are modulated by chemokines, integrins, and selectins and the interaction of these molecules with glycosaminoglycans, predominantly heparan sulfate (HS). The development of HS/heparin mimetics that interfere or inhibit the interactions that occur between glycosaminoglycans and modulators of inflammation holds great potential for use as anti-inflammatory therapeutics. This review will detail the role of HS in the events that occur during inflammation, their interaction and modulation of inflammatory mediators, and the current advances in the development of HS/heparin mimetics as anti-inflammatory biotherapeutics.
引用
收藏
页码:321 / 336
页数:16
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