题名 | Targeting myeloid differentiation protein 2 by the new chalcone L2H21 protects LPS-induced acute lung injury |
作者 | |
发表日期 | 2017-04 |
发表期刊 | JOURNAL OF CELLULAR AND MOLECULAR MEDICINE 影响因子和分区 |
语种 | 英语 |
原始文献类型 | Article |
关键词 | acute lung injury sepsis myeloid differentiation 2 chalcone LPS |
其他关键词 | RECEPTOR 4 ACTIVATION ; INFLAMMATORY RESPONSE ; CYTOKINE PRODUCTION ; TLR4-MD-2 COMPLEX ; MD-2 ; SEPSIS ; TLR4 ; ENDOTOXIN ; BINDING ; MD2 |
摘要 | Acute inflammatory diseases are the leading causes of mortality in intensive care units. Myeloid differentiation 2 (MD-2) is required for recognizing lipopolysaccharide (LPS) by toll-like receptor 4 (TLR4), and represents an attractive therapeutic target for LPS-induced inflammatory diseases. In this study, we report a chalcone derivative, L2H21, as a new MD2 inhibitor, which could inhibit LPS-induced inflammation both in vitro and in vivo. We identify that L2H21 as a direct inhibitor of MD-2 by binding to Arg(90) and Tyr(102) residues in MD-2 hydrophobic pocket using a series of biochemical experiments, including surface plasmon response, molecular docking and amino acid mutation. L2H21 dose dependently inhibited LPS-induced inflammatory cytokine expression in primary macrophages. In mice with LPS intratracheal instillation, L2H21 significantly decreased LPS-induced pulmonary oedema, pathological changes in lung tissue, protein concentration increase in bronchoalveolar lavage fluid, inflammatory cells infiltration and inflammatory gene expression, accompanied with the decrease in pulmonary TLR4/MD-2 complex. Meanwhile, administration with L2H21 protects mice from LPS-induced mortality at a degree of 100%. Taken together, this study identifies a new MD2 inhibitor L2H21 as a promising candidate for the treatment of acute lung injury (ALI) and sepsis, and validates that inhibition of MD-2 is a potential therapeutic strategy for ALI. |
资助项目 | National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [81503123, 21272179, 81570027]; Zhejiang Natural Science Funding [LY14C050004, LY13H060007, LQ15H120005] |
出版者 | WILEY |
出版地 | HOBOKEN |
ISSN | 1582-4934 |
EISSN | 1582-4934 |
卷号 | 21期号:4页码:746-757 |
DOI | 10.1111/jcmm.13017 |
页数 | 12 |
WOS类目 | Cell Biology ; Medicine, Research & Experimental |
WOS研究方向 | Cell Biology ; Research & Experimental Medicine |
WOS记录号 | WOS:000399310800012 |
收录类别 | SCIE ; PUBMED ; SCOPUS |
URL | 查看原文 |
PubMed ID | 27860279 |
PMC记录号 | PMC5345657 |
SCOPUSEID | 2-s2.0-85003781848 |
通讯作者地址 | [Liu, Xing]Chemical Biology Research Center,School of Pharmaceutical Sciences,Wenzhou Medical University,Wenzhou,China |
Scopus学科分类 | Molecular Medicine;Cell Biology |
TOP期刊 | TOP期刊 |
引用统计 | |
文献类型 | 期刊论文 |
条目标识符 | https://kms.wmu.edu.cn/handle/3ETUA0LF/1091 |
专题 | 药学院(分析测试中心)_生物有机与药物化学研究中心 附属第二医院 附属第一医院 第二临床医学院、附属第二医院、育英儿童医院 口腔医学院、附属口腔医院 第一临床医学院(信息与工程学院)、附属第一医院_外科学_整形外科 |
通讯作者 | Liu, Xing |
作者单位 | 1.Chemical Biology Research Center,School of Pharmaceutical Sciences,Wenzhou Medical University,Wenzhou,China; 2.The Second Affiliated Hospital,Wenzhou Medical University,Wenzhou,China; 3.Department of Orthopedic Surgery,The First Affiliated Hospital,Wenzhou Medical University,Wenzhou,China; 4.Department of Oral Prophylaxis and Hygiene,School and Hospital of Stomatology,Wenzhou Medical University,Wenzhou,China |
第一作者单位 | 药学院(分析测试中心); 生物有机与药物化学研究中心 |
通讯作者单位 | 药学院(分析测试中心); 生物有机与药物化学研究中心 |
第一作者的第一单位 | 药学院(分析测试中心) |
推荐引用方式 GB/T 7714 | Zhang, Yali,Xu, Tingting,Wu, Beibei,et al. Targeting myeloid differentiation protein 2 by the new chalcone L2H21 protects LPS-induced acute lung injury[J]. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE,2017,21(4):746-757. |
APA | Zhang, Yali., Xu, Tingting., Wu, Beibei., Chen, Hongjin., Pan, Zheer., ... & Liang, Guang. (2017). Targeting myeloid differentiation protein 2 by the new chalcone L2H21 protects LPS-induced acute lung injury. JOURNAL OF CELLULAR AND MOLECULAR MEDICINE, 21(4), 746-757. |
MLA | Zhang, Yali,et al."Targeting myeloid differentiation protein 2 by the new chalcone L2H21 protects LPS-induced acute lung injury".JOURNAL OF CELLULAR AND MOLECULAR MEDICINE 21.4(2017):746-757. |
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