Chitosan accelerates the production of osteopontin from polymorphonuclear leukocytes

被引:54
作者
Ueno, H
Murakami, M
Okumura, M
Kadosawa, T
Uede, T
Fujinaga, T [1 ]
机构
[1] Hokkaido Univ, Grad Sch Vet Med, Dept Vet Clin Sci, Lab Vet Surg, Sapporo, Hokkaido 0600818, Japan
[2] Hokkaido Univ, Inst Med Genet, Sect Immunopathogenesis, Sapporo, Hokkaido 0600818, Japan
关键词
osteopontin; polymorphonuclear leukocyte; wound healing; chitosan;
D O I
10.1016/S0142-9612(00)00328-8
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Chitosan is a copolymer of beta (1 --> 4) glucosamine and N-acetyl-D-glucosamine, which accelerates the infiltration of polymorphonuclear leukocytes (PMN) in the early phase of wound healing. In the granulation tissue treated with chitosan in canine experimental wound, osteopontin (OPN) was strongly positive in PMN immunohistochemically. OPN is a glycosylated phosphoprotein and promotes the attachment or spread of a variety of cell types. In addition, OPN may play a role in granulomatous inflammation. Production of OPN in PMN was therefore investigated in vitro using human PMN in this study. PMN stimulated with granulocyte-colony stimulating factor (G-CSF) and chitosan accumulated OPN mRNA, and released OPN into their culture supernatants. These findings suggest that OPN is synthesized by migrating PMN which plays the novel role of regulating the evolution of wound healing with chitosan treatment at the early phase of healing, (C) 2001 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:1667 / 1673
页数:7
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