A polysaccharide isolated from the fruits of Physalis alkekengi L. induces RAW264.7 macrophages activation via TLR2 and TLR4-mediated MAPK and NF-κB signaling pathways

被引:80
作者
Yang, Fan [1 ]
Li, Xiaozhou [1 ]
Yang, Ye [1 ]
Ayivi-Tosuh, Selina Mawunyo [1 ]
Wang, Feihe [1 ]
Li, Hong [1 ]
Wang, Guiyun [1 ]
机构
[1] Northeast Normal Univ, Sch Life Sci, 5268 Renmin St, Changchun 130024, Jilin, Peoples R China
关键词
Physalis alkekengi L; Polysaccharide; RAW264.7; macrophages; PATTERN-RECOGNITION RECEPTORS; INNATE IMMUNITY; STRUCTURAL-CHARACTERIZATION;
D O I
10.1016/j.ijbiomac.2019.08.174
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
Polysaccharides from Physalis alkekengi L. have been proven to possess many biological activities. In our previous study, a homogeneous polysaccharide (PPSB) was extracted and purified from the fruits of Physalis alkekengi L., and the structure characterization was analyzed. The present study aimed to investigate the effects of PPSB on RAW264.7 macrophage cells activation and the underlying molecular mechanism. PPSB could activate RAW264.7 cells by not only enhancing the pinocytic and phagocytic activity, but also promoting the production of NO, ROS, TNF-alpha, and IL-6 in RAW264.7 cells. Meanwhile, PPSB up-regulated the expression of major histocompatibility complex (MHC-I/II) and costimulatory molecules such as CD40, CD80 and CD86. Mechanism studies showed that PPSB induced the activation of mitogen-activated protein kinases (MAPKs) and nuclear factor-kappa B (NF-kappa B) pathways. Moreover, the production of NO, TNF-alpha and IL-6 induced by PPSB in RAW264.7 cells were suppressed by specific MAPKs and NF-kappa B inhibitors. Further experiments with blocking antibodies demonstrated that the releases of NO, INF-alpha and IL-6 and the activation of MAPKs and NF-kappa B induced by PPSB were decreased after TLR2 and TLR4 were blocked. Our date illustrated that PPSB was capable of activating the RAW264.7 cells via MAPKs and NF-kappa B signaling mediated by TLR2 and TLR4. (C) 2019 Elsevier B.V. All rights reserved.
引用
收藏
页码:895 / 906
页数:12
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