Syndecans in Inflammation at a Glance

被引:89
作者
Gopal, Sandeep [1 ]
机构
[1] Monash Univ, Monash Biomed Discovery Inst, Dept Anat & Dev Biol, Dev & Stem Cells Program, Melbourne, Vic, Australia
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
基金
澳大利亚研究理事会; 英国医学研究理事会;
关键词
syndecan; proteoglycan; extravasation; inflammation; shedding; cytokines; chemokine gradient; LEUKOCYTE-ENDOTHELIAL INTERACTIONS; HEPARAN-SULFATE; SOLUBLE SYNDECAN-1; MATRIX METALLOPROTEINASES; EXTRACELLULAR-MATRIX; CYTOKINE REGULATION; CELL-ADHESION; WOUND REPAIR; EXPRESSION; ANGIOGENESIS;
D O I
10.3389/fimmu.2020.00227
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Syndecans are transmembrane proteoglycans with heparan and chondroitin sulfate chains attached to their extracellular domain. Like many proteoglycans, they interact with a large number of ligands, such as growth factors, adhesion receptors, soluble small molecules, proteinases, and other extracellular matrix proteins to initiate downstream signaling pathways. Syndecans play a major role in inflammation, mainly by regulating leukocyte extravasation and cytokine function. At the same time, syndecans can undergo cytokine mediated changes in their expression levels during inflammation. The function of syndecans during inflammation appears to depend on the stage of inflammation, sulfation of heparan/chondroitin sulfate chains, the rate of ectodomain shedding and the solubility of the ectodomains. From the current literature, it is clear that syndecans are not only involved in the initial recruitment of pro-inflammatory molecules but also in establishing a balanced progression of inflammation. This review will summarize how cell surface and soluble syndecans regulate multiple aspects of inflammation.
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页数:8
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