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Molecular Weight-Dependent Immunostimulative Activity of Low Molecular Weight Chitosan via Regulating NF-κB and AP-1 Signaling Pathways in RAW264.7 Macrophages

机译:低分子量壳聚糖通过调节RAW264.7巨噬细胞中的NF-κB和AP-1信号通路的分子量依赖性免疫刺激活性。

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摘要

Chitosan and its derivatives such as low molecular weight chitosans (LMWCs) have been found to possess many important biological properties, such as antioxidant and antitumor effects. In our previous study, LMWCs were found to elicit a strong immunomodulatory response in macrophages dependent on molecular weight. Herein we further investigated the molecular weight-dependent immunostimulative activity of LMWCs and elucidated its mechanism of action on RAW264.7 macrophages. LMWCs (3 kDa and 50 kDa of molecular weight) could significantly enhance the mRNA expression levels of COX-2, IL-10 and MCP-1 in a molecular weight and concentration-dependent manner. The results suggested that LMWCs elicited a significant immunomodulatory response, which was dependent on the dose and the molecular weight. Regarding the possible molecular mechanism of action, LMWCs promoted the expression of the genes of key molecules in NF-κB and AP-1 pathways, including IKKβ, TRAF6 and JNK1, and induced the phosphorylation of protein IKBα in RAW264.7 macrophage. Moreover, LMWCs increased nuclear translocation of p65 and activation of activator protein-1 (AP-1, C-Jun and C-Fos) in a molecular weight-dependent manner. Taken together, our findings suggested that LMWCs exert immunostimulative activity via activation of NF-κB and AP-1 pathways in RAW264.7 macrophages in a molecular weight-dependent manner and that 3 kDa LMWC shows great potential as a novel agent for the treatment of immune suppression diseases and in future vaccines.
机译:已经发现壳聚糖及其衍生物,例如低分子量壳聚糖(LMWC)具有许多重要的生物学特性,例如抗氧化剂和抗肿瘤作用。在我们先前的研究中,发现LMWCs依赖于分子量在巨噬细胞中引起强烈的免疫调节反应。在本文中,我们进一步研究了LMWCs的分子量依赖性免疫刺激活性,并阐明了其对RAW264.7巨噬细胞的作用机理。 LMWC(分子量为3 kDa和50 kDa)可以以分子量和浓度依赖性的方式显着提高COX-2,IL-10和MCP-1的mRNA表达水平。结果表明,LMWCs引发了显着的免疫调节反应,这取决于剂量和分子量。关于可能的作用机理,LMWCs促进了IK-β,TRAF6和JNK1等NF-κB和AP-1途径中关键分子基因的表达,并诱导RAW264.7巨噬细胞中的蛋白IKBα磷酸化。此外,LMWCs以分子量依赖性方式增加p65的核易位和激活蛋白1(AP-1,C-Jun和C-Fos)的活化。综上所述,我们的发现表明,LMWCs通过激活RAW264.7巨噬细胞中的NF-κB和AP-1途径以分子量依赖性方式发挥免疫刺激活性,并且3 kDa LMWC显示出巨大的潜力,可作为一种新型药物治疗免疫抑制疾病和未来的疫苗。

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