Regulation of M1/M2 macrophage polarization by Sutherlandia frutescens via NFkB and MAPK signaling pathways

被引:13
|
作者
Camille, N. [1 ]
Dealtry, G. [1 ]
机构
[1] Nelson Mandela Univ, Dept Biochem, POB 77000, ZA-6031 Port Elizabeth, South Africa
基金
新加坡国家研究基金会;
关键词
Sutherlandia frutescens; Macrophage; RAW 264.7 cell line; Inflammation; Type; 2; Diabetes; KAPPA-B; INFLAMMATORY RESPONSE; MURINE MACROPHAGES; DIABETIC-RATS; EXTRACTS; M2; ACTIVATION; INHIBITION; CYTOKINES; OBESITY;
D O I
10.1016/j.sajb.2018.02.400
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Sutherlandia frutescens is a medicinal plant, indigenous to South Africa, used to treat a number of conditions, including Type 2 Diabetes (T2D) and immune disorders. It is thought to have the capacity to regulate macrophage differentiation, thus impacting upon metabolic immune diseases and indicating a potential for ethnopharmaceutical use. In this paper we report the molecular action of S. fiutescens with regard to in vitro macrophage differentiation and potential functions in vivo involving inflammation and wound healing. The responses of cells of the RAW 264.7 murine macrophage cell line (a model for macrophage function) to hot aqueous or 100% ethanol extracts of S. frutescens prepared from a single plant source previously shown to target T2D were compared to determine the relative efficacy and action of each extract. Activation of the proinflammatory M1 phenotype and the anti-inflammatory M2 phenotype was investigated using the CD markers CD86 (M1) and CD206 (M2). Both S. frutescens extracts down-regulated CD86 expression, and the ethanolic extract up-regulated CD206, indicating stimulation of the M2 phenotype over the M1 phenotype. M1 macrophage pro-inflammatory responses in vitro, including nitric oxide and reactive oxygen species production and cyclo-oxygenase-2 (COX-2) expression were inhibited by both extracts.This is the first report of down regulation by S. frutescens of COX-2, a major pro-inflammatory mediator. Patterns of cytokine production determined by ELISA assays, showed down-regulation of the M1 pro-inflammatory cytokine profile, whilst the M2 cytokine profile remained unchanged. Reduced production of inflammatory mediators was associated with decreased activity of the mitogen activated protein kinases (MAPKs) and nuclear factor kappa-light-chain-enhancer of activated B-cells (NF kappa B) signalling pathways. This novel finding in an in vitro model of macrophage responses to S. frutescens leads to the hypothesis that several medicinal properties of S. frutescens extracts are mediated by regulation of MAPK and NF kappa B cell signaling pathways leading to a reduction in MI macrophage activity and redirection towards M2 anti-inflammatory functions, thus promoting tissue remodeling and immune regulation. (C) 2018 SAAB. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 51
页数:10
相关论文
共 50 条
  • [21] Regulatory Effects of Quercetin on M1/M2 Macrophage Polarization and Oxidative/Antioxidative Balance
    Tsai, Cheng-Fang
    Chen, Guan-Wei
    Chen, Yen-Chang
    Shen, Ching-Kai
    Lu, Dah-Yuu
    Yang, Liang-Yo
    Chen, Jia-Hong
    Yeh, Wei-Lan
    NUTRIENTS, 2022, 14 (01)
  • [22] Quercetin ameliorates kidney injury and fibrosis by modulating M1/M2 macrophage polarization
    Lu, Hong
    Wu, Lianfeng
    Liu, Leping
    Ruan, Qingqing
    Zhang, Xing
    Hong, Weilong
    Wu, Shijia
    Jin, Guihua
    Bai, Yongheng
    BIOCHEMICAL PHARMACOLOGY, 2018, 154 : 203 - 212
  • [23] Irgm1 promotes M1 but not M2 macrophage polarization in atherosclerosis pathogenesis and development
    Fang, Shaohong
    Xu, Yanwen
    Zhang, Yun
    Tian, Jiangtian
    Li, Ji
    Li, Zhaoying
    He, Zhongze
    Chai, Ruikai
    Liu, Fang
    Zhang, Tongshuai
    Yang, Shuang
    Pei, Chunying
    Liu, Xinxin
    Lin, Peng
    Xu, Hongwei
    Yu, Bo
    Li, Hulun
    Sun, Bo
    ATHEROSCLEROSIS, 2016, 251 : 282 - 290
  • [24] AhR activation attenuates calcium oxalate nephrocalcinosis by diminishing M1 macrophage polarization and promoting M2 macrophage polarization
    Yang, Xiaoqi
    Liu, Haoran
    Ye, Tao
    Duan, Chen
    Lv, Peng
    Wu, Xiaoliang
    Liu, Jianhe
    Jiang, Kehua
    Lu, Hongyan
    Yang, Huan
    Xia, Ding
    Peng, Ejun
    Chen, Zhiqiang
    Tang, Kun
    Ye, Zhangqun
    THERANOSTICS, 2020, 10 (26): : 12011 - 12025
  • [25] Progranulin inhibits LPS-induced macrophage M1 polarization via NF-kB and MAPK pathways
    Liu, Lianlian
    Guo, Hongmei
    Song, Aimei
    Huang, Jiahui
    Zhang, Yu
    Jin, Shanshan
    Li, Shutong
    Zhang, Liguo
    Yang, Chengzhe
    Yang, Pishan
    BMC IMMUNOLOGY, 2020, 21 (01)
  • [26] Glucocorticoids improve the balance of M1/M2 macrophage polarization in experimental autoimmune uveitis through the P38MAPK-MEF2C axis
    Qu, Ruyi
    Zhou, Mengxian
    Qiu, Yan
    Peng, Yuan
    Yin, Xuewei
    Liu, Bin
    Bi, Hongsheng
    Gao, Yan'e
    Guo, Dadong
    INTERNATIONAL IMMUNOPHARMACOLOGY, 2023, 120
  • [27] YAP Deficiency Attenuates Pulmonary Injury Following Mechanical Ventilation Through the Regulation of M1/M2 Macrophage Polarization
    Luo, Qiong
    Luo, Jing
    Wang, Yanlin
    JOURNAL OF INFLAMMATION RESEARCH, 2020, 13 : 1279 - 1290
  • [28] Effects of Xenoestrogens in Human M1 and M2 Macrophage Migration, Cytokine Release, and Estrogen-Related Signaling Pathways
    Teixeira, Diana
    Marques, Claudia
    Pestana, Diogo
    Faria, Ana
    Norberto, Sonia
    Calhau, Conceicao
    Monteiro, Rosario
    ENVIRONMENTAL TOXICOLOGY, 2016, 31 (11) : 1496 - 1509
  • [29] Targeting MAPK Pathways by Naringenin Modulates Microglia M1/M2 Polarization in Lipopolysaccharide-Stimulated Cultures
    Zhang, Bei
    Wei, Yi-Zheng
    Wang, Guo-Qing
    Li, Dai-Di
    Shi, Jing-Shan
    Zhang, Feng
    FRONTIERS IN CELLULAR NEUROSCIENCE, 2019, 12
  • [30] Exploring the polarization of M1 and M2 macrophages in the context of skin diseases
    Apeku, Ernestina
    Tantuoyir, Marcarious M.
    Zheng, Rui
    Tanye, Nestor
    MOLECULAR BIOLOGY REPORTS, 2024, 51 (01)