Hyun-Ja Jeong , Hyun-Na Koo , Eun-Young Oh , Han-Jung Chae , Hyung-Ryong Kim , Sang-Bong Suh , Cheorl-Ho Kim , Kwang-Ho Cho , Byung-Rim Park , Seung-Taeck Park , Young-Mi Lee , Hyung-Min Kim
{"title":"Nitric oxide production by high molecular weight water-soluble chitosan via nuclear factor-κB activation","authors":"Hyun-Ja Jeong , Hyun-Na Koo , Eun-Young Oh , Han-Jung Chae , Hyung-Ryong Kim , Sang-Bong Suh , Cheorl-Ho Kim , Kwang-Ho Cho , Byung-Rim Park , Seung-Taeck Park , Young-Mi Lee , Hyung-Min Kim","doi":"10.1016/S0192-0561(00)00055-2","DOIUrl":null,"url":null,"abstract":"<div><p><span>High molecular weight water-soluble chitosan (WSC), having an average molecular weight of 300 000 Da and a degree of deacethylation over 90%, can be produced using a simple multi-step membrane separation process. In this study, the effect of WSC on the production of nitric oxide (NO) in RAW 264.7 macrophages was evaluated. Water-insoluble chitosan alone has been previously shown to exhibit in vitro stimulatory effect on macrophages NO production. However, WSC had no effect on NO production by itself. When WSC was used in combination with recombinant interferon-γ (rIFN-γ), there was a marked cooperative induction of NO synthesis in a dose-dependent manner. The optimal effect of WSC on NO synthesis was shown 24 h after treatment with rIFN-γ. The increased production of NO from rIFN-γ plus WSC-stimulated RAW 264.7 macrophages was decreased by the treatment with </span><em>N</em><sup><em>G</em></sup>-monomethyl-<span>l</span>-arginine (<em>N</em><sup>G</sup><span>MMA). The increase in NO synthesis was reflected, as an increased amounts of inducible NO synthase<span> protein. In addition, synergy between rIFN-γ and WSC was mainly dependent on WSC-induced tumor necrosis factor-α (TNF-α) and nuclear factor-κB (NF-κB) activation. The present results indicate that the capacity of WSC to increase NO production from rIFN-γ-primed RAW 264.7 macrophages is the result of WSC-induced TNF-α secretion via the signal transduction pathway of NF-κB activation.</span></span></p></div>","PeriodicalId":14002,"journal":{"name":"International journal of immunopharmacology","volume":"22 11","pages":"Pages 923-933"},"PeriodicalIF":0.0000,"publicationDate":"2000-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S0192-0561(00)00055-2","citationCount":"41","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"International journal of immunopharmacology","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0192056100000552","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 41
Abstract
High molecular weight water-soluble chitosan (WSC), having an average molecular weight of 300 000 Da and a degree of deacethylation over 90%, can be produced using a simple multi-step membrane separation process. In this study, the effect of WSC on the production of nitric oxide (NO) in RAW 264.7 macrophages was evaluated. Water-insoluble chitosan alone has been previously shown to exhibit in vitro stimulatory effect on macrophages NO production. However, WSC had no effect on NO production by itself. When WSC was used in combination with recombinant interferon-γ (rIFN-γ), there was a marked cooperative induction of NO synthesis in a dose-dependent manner. The optimal effect of WSC on NO synthesis was shown 24 h after treatment with rIFN-γ. The increased production of NO from rIFN-γ plus WSC-stimulated RAW 264.7 macrophages was decreased by the treatment with NG-monomethyl-l-arginine (NGMMA). The increase in NO synthesis was reflected, as an increased amounts of inducible NO synthase protein. In addition, synergy between rIFN-γ and WSC was mainly dependent on WSC-induced tumor necrosis factor-α (TNF-α) and nuclear factor-κB (NF-κB) activation. The present results indicate that the capacity of WSC to increase NO production from rIFN-γ-primed RAW 264.7 macrophages is the result of WSC-induced TNF-α secretion via the signal transduction pathway of NF-κB activation.