首站-论文投稿智能助手
典型文献
Sulforaphane attenuates dextran sodium sulphate induced intestinal infl ammation via IL-10/STAT3 signaling mediated macrophage phenotype switching
文献摘要:
Innate immunity, particularly macrophages, is critical for intestinal homeostasis. Sulforaphane, a dietary isothiocyanate from cruciferous vegetables, has been reported to protect against intestinal inflammation. However, the role of macrophages in sulforaphane mediated intestinal inflammation and the underlying molecular mechanisms have not been studied yet. In this study, sulforaphane effectively attenuated dextran sodium sulphate (DSS) induced intestinal inflammation in murine model. Of note, sulforaphane skewed the switching from classically (M1) to alternatively (M2) activated phenotype both in intestinal and bone marrow-derived macrophages (BMDMs). The expression levels of M1 associated maker genes induced by DSS or lipopolysaccharide (LPS) plus interferon gamma-γ (IFN-γ) were suppressed by sulforaphane while M2 marker gene expression levels were improved. This resulted in alteration of inflammatory mediators, particularly interleukin-10 (IL-10), both in colon tissues and culture medium of BMDMs. Subsequently, IL-10 was found to mediate the sulforaphane induced M2 phenotype switching of BMDMs through the activation of STAT3 signaling. This was confirmed by immunofluorescence analysis with increased number of p-STAT3-positive cells in the colon sections. Moreover, anti-IL-10 neutralizing antibody significantly interfered M2 phenotyping of BMDMs induced by sulforaphane with reduced STAT3 phosphorylation. Findings here introduced a potential utilization of sulforaphane for intestinal inflammation treatment with macrophages as the therapeutic targets.
文献关键词:
作者姓名:
Yuyang Sun;Jiqing Tang;Cui Li;Jun Liu;Haijie Liu
作者机构:
College of Food Science and Nutritional Engineering,China Agricultural University,Beijing 100083,China;Beijing Advanced Innovation Center for Food Nutrition and Human Health,Beijing Technology and Business University,Beijing 100048,China
引用格式:
[1]Yuyang Sun;Jiqing Tang;Cui Li;Jun Liu;Haijie Liu-.Sulforaphane attenuates dextran sodium sulphate induced intestinal infl ammation via IL-10/STAT3 signaling mediated macrophage phenotype switching)[J].食品科学与人类健康(英文),2022(01):129-142
A类:
Sulforaphane,infl,ammation
B类:
attenuates,dextran,sodium,sulphate,induced,intestinal,via,STAT3,signaling,mediated,phenotype,switching,Innate,immunity,particularly,macrophages,critical,homeostasis,dietary,isothiocyanate,from,cruciferous,vegetables,has,been,reported,protect,against,inflammation,However,role,sulforaphane,underlying,molecular,mechanisms,have,studied,yet,this,study,effectively,attenuated,DSS,murine,model,Of,note,skewed,classically,M1,alternatively,M2,activated,both,bone,marrow,derived,BMDMs,expression,levels,associated,maker,genes,by,lipopolysaccharide,LPS,plus,interferon,gamma,IFN,were,suppressed,while,marker,improved,This,resulted,alteration,inflammatory,mediators,interleukin,colon,tissues,culture,medium,Subsequently,was,found,through,activation,confirmed,immunofluorescence,analysis,increased,number,positive,cells,sections,Moreover,neutralizing,antibody,significantly,interfered,phenotyping,reduced,phosphorylation,Findings,here,introduced,potential,utilization,treatment,therapeutic,targets
AB值:
0.563339
相似文献
Spirulina platensis aqueous extracts ameliorate colonic mucosal damage and modulate gut microbiota disorder in mice with ulcerative colitis by inhibiting inflammation and oxidative stress
Jian WANG;Liqian SU;Lun ZHANG;Jiali ZENG;Qingru CHEN;Rui DENG;Ziyan WANG;Weidong KUANG;Xiaobao JIN;Shuiqing GUI;Yinghua XU;Xuemei LU-Guangdong Provincial Key Laboratory of Pharmaceutical Bioactive Substances,School of Life Science and Biopharmaceutics,Guangdong Pharmaceutical University,Guangzhou 510006,China;School of Pharmacy,Guangdong Pharmaceutical University,Guangzhou 510006,China;Intensive Care Unit,Shenzhen Second People's Hospital,the First Affiliated Hospital of Shenzhen University,Shenzhen 518031,China;Key Laboratory of the Ministry of Health for Research on Quality and Standardization of Biotech Products,National Institutes for Food and Drug Control,Beijing 102629,China
Taxifolin attenuates inflammation via suppressing MAPK signal pathway in vitro and in silico analysis
Xingyan Zhang;Xiaoyan Lian;Huling Li;Wenjing Zhao;Xin Li;Fujun Zhou;Yutong Zhou;Tao Cui;Yuli Wang;Changxiao Liu-Key Laboratory of Quality-marker of Traditional Chinese Medicines,Tianjin Institute of Pharmaceutical Research Co.,Ltd.,Tianjin 300462,China;Center for Drug Evaluation,National Medical Products Administration,Beijing 100022,China;Department of Pharmacology,Tianjin Medical University,Tianjin 300070,China;State Key Laboratory of Drug Delivery Technology and Pharmacokinetics,Tianjin Institute of Pharmaceutical Research Co.,Ltd.,Tianjin 300462,China;Key Laboratory of Systems Bioengineering(Ministry of Education),School of Chemistry Engineering and Technology,Tianjin University,Tianjin 300072,China;Pharmaceuticai Armaceuticai DA REN TANG Group Corporation Limited Traditional Chinese Pharmacy Researchinstitute,Tianjin 300457,China;Tianjin Key Laboratory of Quality Control in Chinese Medicine,Tianjin 300457,China;Research Unit for Drug Metabolism,Chinese Academy of Medical Sciences,Beijing 100730,China
Sulforaphane ameliorates non-alcoholic fatty liver disease in mice by promoting FGF21/FGFR1 signaling pathway
Yi-kuan Wu;Zheng-nan Ren;Sheng-long Zhu;Yun-zhou Wu;Gang Wang;Hao Zhang;Wei Chen;Zhao He;Xian-long Ye;Qi-xiao Zhai-State Key Laboratory of Food Science and Technology,Jiangnan University,Wuxi 214122,China;School of Food Science and Technology,Jiangnan University,Wuxi 214122,China;School of Medicine,Jiangnan University,Wuxi 214122,China;College of Life Science,Northeast Agricultural University,Harbin 150038,China;National Engineering Research Center for Functional Food,Jiangnan University,Wuxi 214122,China;Shandong Key Laboratory of Endocrinology and Lipid Metabolism,Jinan 250021,China;School of Medicine,Shandong University,Jinan 250012,China;Ganjiang Chinese Medicine Innovation Center,Nanchang 330000,China
GPR84 signaling promotes intestinal mucosal inflammation via enhancing NLRP3 inflammasome activation in macrophages
Qing Zhang;Lin-hai Chen;Hui Yang;You-chen Fang;Si-wei Wang;Min Wang;Qian-ting Yuan;Wei Wu;Yang-ming Zhang;Zhan-ju Liu;Fa-jun Nan;Xin Xie-State Key Laboratory of Drug Research,The National Center for Drug Screening,Shanghai Institute of Materia Medica,Chinese Academy of Sciences,Shanghai 201203,China;School of Pharmaceutical Science and Technology,Hangzhou Institute for Advanced Study,University of Chinese Academy of Sciences,Hangzhou 310024,China;University of Chinese Academy of Sciences,Beijing 100049,China;Department of Gastroenterology,The Shanghai Tenth People's Hospital,Tongji University,Shanghai 200072,China;Burgeon Therapeutics Co.,Ltd,Shanghai 201203,China;Yantai Key Laboratory of Nanomedicine and Advanced Preparations,Yantai Institute of Materia Medica,Yantai 264000,China
机标中图分类号,由域田数据科技根据网络公开资料自动分析生成,仅供学习研究参考。