4.7 Article

An iminosugar-based heparanase inhibitor heparastatin (SF4) suppresses infiltration of neutrophils and monocytes into inflamed dorsal air pouches

期刊

INTERNATIONAL IMMUNOPHARMACOLOGY
卷 35, 期 -, 页码 15-21

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.intimp.2016.03.017

关键词

Heparanase; Heparastatin (SF4); Extracellular matrix; Chemokines

资金

  1. Ministry of Education, Science, Sports and Culture of Japan [16390033, 17046002, 18390041, 19659012, 22390023, 25460165]
  2. Japan Society for the Promotion of Science JSPS [S-10206]
  3. Global COE Program Medical System Innovation on Multidisciplinary Integration from MEXT, Japan
  4. Grants-in-Aid for Scientific Research [26670023, 17046002, 22390023, 16390033, 25460165, 19659012, 18390041] Funding Source: KAKEN

向作者/读者索取更多资源

Local infiltration of inflammatory cells is regulated by a number of biological steps during which the cells likely penetrate through subendothelial basement membranes that contain heparan sulfate proteoglycans. In the present study, we examined whether administration of heparastatin (SF4), an iminosugar-based inhibitor of heparanase, could suppress local inflammation and degradation of heparan sulfate proteoglycans in basement membranes. In a carrageenan- or formyl peptide-induced dorsal air pouch inflammation model, the number of infiltrated neutrophils and monocytes was significantly lower in mice after topical administration of heparastatin (SF4). The concentration of chemokines MIP-2 and KC in pouch exudates of drug-treated mice was similar to controlin a zymosan-induced peritonitis model, the number of infiltrated cells was not altered in drug-treated mice. To further test how heparastatin (SF4) influences transmigration of inflammatory neutrophils, its suppressive effect on migration and matrix degradation was examined in vitro. In the presence of heparastatin (SF4), the number of neutrophils that infiltrated across a Matrigel-coated polycarbonate membrane was significantly lower, while the number of neutrophils passing through an uncoated membrane was not altered. Lysate of bone marrow-derived neutrophils released sulfate-radiolabeled macromolecules from basement membrane-like extracellular matrix, which was suppressed by heparastatin (SF4). Heparan sulfate degradation activity was almost completely abolished after incubation of lysate with protein G-conjugated anti-heparanase monoclonal antibody, strongly suggesting that the activity was due to heparanase-mediated degradation. Taken together, in a dorsal air pouch inflammation model heparastatin (SF4) potentially suppresses extravasation of inflammatory cells by impairing the degradation of basement membrane heparan sulfate. (C) 2016 Elsevier B.V. All rights reserved,

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