Nitric oxide production by high molecular weight water-soluble chitosan via nuclear factor-κB activation

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
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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.

核因子-κB活化高分子量水溶性壳聚糖制备一氧化氮
采用简单的多步骤膜分离工艺可制得高分子量水溶性壳聚糖(WSC),其平均分子量为30万Da,脱乙酰度达90%以上。在本研究中,我们评估了WSC对RAW 264.7巨噬细胞一氧化氮(NO)产生的影响。不溶于水的壳聚糖在体外对巨噬细胞产生一氧化氮有刺激作用。然而,WSC本身对no的产生没有影响。当WSC与重组干扰素-γ (rIFN-γ)联合使用时,以剂量依赖的方式显著协同诱导NO合成。在rIFN-γ作用24 h后,WSC对NO合成的影响达到最佳。ng - monmethyl -l-arginine (NGMMA)处理后,rIFN-γ和wsc刺激的RAW 264.7巨噬细胞产生的NO增加减少。一氧化氮合成的增加表现为诱导的一氧化氮合酶蛋白量的增加。此外,rIFN-γ与WSC的协同作用主要依赖于WSC诱导的肿瘤坏死因子-α (TNF-α)和核因子-κB (NF-κB)的活化。本研究结果表明,WSC增加rIFN-γ-引物RAW 264.7巨噬细胞NO生成的能力是WSC通过NF-κB活化信号转导途径诱导TNF-α分泌的结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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