Effect of chitosan molecular weight on anti-inflammatory activity in the RAW 264.7 macrophage model

被引:126
作者
Chang, Shun-Hsien [1 ]
Lin, Yi-Yung [1 ]
Wu, Guan-James [2 ]
Huang, Chung-Hsiung [1 ]
Tsai, Guo Jane [1 ,3 ]
机构
[1] Natl Taiwan Ocean Univ, Dept Food Sci, 2 Pei Ning Rd, Keelung 202, Taiwan
[2] Natl Penghu Univ Sci & Technol, Dept Food Sci, Penghu, Taiwan
[3] Natl Taiwan Ocean Univ, Ctr Marine Bioenvironm & Biotechnol, Keelung, Taiwan
关键词
Chitosan; RAW; 264.7; macrophages; Inflammation; Cytokines; Mitogen-activated protein kinase; ACTIVATED PROTEIN-KINASES; ANTIMICROBIAL ACTIVITY; EXPRESSION; CYTOKINE; LIPOPOLYSACCHARIDE; INFLAMMATION; CELLS; IL-6; P38; INTERLEUKIN-6;
D O I
10.1016/j.ijbiomac.2019.02.066
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Chitosan (300 kDa) was degraded by cellulase to chitosans with molecular weights (MWs) of 156, 72, 7.1, and 3.3 kDa and a chitooligosaccharide mixture (COS). Effects of these on NO secretion, cytokine production, and mitogen-activated protein kinase pathways in lipopolysaccharide (LPS)-induced murine RAW 264.7 macrophages were investigated. Larger chitosans (300, 156, 72 kDa) significantly inhibited NO production, whereas smaller chitosans (7.1 & 33 kDa, COS) increased NO production. The 156 and 72 kDa chitosans significantly inhibited TNF-alpha and IL-6 production, whereas the 7.1 kDa chitosan and COS significantly induced their production. The 156 and 72 kDa chitosans inhibited NF-kappa B activation and iNOS expression by binding to the CR3 (for 156 kDa chitosan), or CR3 and TLR4 receptor (for 72 kDa chitosan). The smaller chitosans (e.g. 7.1 kDa chitosan and COS) activated NF-kappa B and enhanced iNOS expression by binding to CD14, TLR4, and CR3 receptors to activate JNK signaling proteins. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:167 / 175
页数:9
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