Tetrahydroisoquinolines: New Inhibitors of Neutrophil Extracellular Trap (NET) Formation

被引:23
|
作者
Martinez, Nancy E. [1 ,2 ,3 ]
Zimmermann, Tobias J. [1 ,2 ]
Goosmann, Christian [3 ]
Alexander, Tobias [4 ]
Hedberg, Christian [5 ]
Ziegler, Slava [1 ]
Zychlinsky, Arturo [3 ]
Waldmann, Herbert [1 ,2 ]
机构
[1] Max Planck Inst Mol Physiol, Dept Chem Biol, Otto Hahn Str 11, D-44227 Dortmund, Germany
[2] Tech Univ Dortmund, Fak Chem, Lehrbereich Chem Biol, Otto Hahn Str 6, D-44227 Dortmund, Germany
[3] Max Planck Inst Infect Biol, Dept Cellular Microbiol, Charitepl 1,Campus Charite Mitte, D-10117 Berlin, Germany
[4] Univ Med Berlin, CCM, Dept Rheumatol & Clin Immunol, Charitepl 1, D-10117 Berlin, Germany
[5] Umea Univ, KBC, Umea Ctr Microbial Res, Dept Chem, C4 Linnaeus Vag 10, S-90187 Umea, Sweden
基金
欧洲研究理事会;
关键词
inhibitors; NETosis; neutrophil extracellular traps (NETs); structure-activity relationships; tetrahydroisoquinolines; BIOLOGY-ORIENTED SYNTHESIS; MYELOPEROXIDASE; RELEASE; DNA; ELASTASE; IMMUNITY; MECHANISMS; PHAGOSOME;
D O I
10.1002/cbic.201600650
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
Neutrophils are short-lived leukocytes that migrate to sites of infection as part of the acute immune response, where they phagocytose, degranulate, and form neutrophil extracellular traps (NETs). During NET formation, the nuclear lobules of neutrophils disappear and the chromatin expands and, accessorized with neutrophilic granule proteins, is expelled. NETs can be pathogenic in, for example, sepsis, cancer, and autoimmune and cardiovascular diseases. Therefore, the identification of inhibitors of NET formation is of great interest. Screening of a focused library of natural-product-inspired compounds by using a previously validated phenotypic NET assay identified a group of tetrahydroisoquinolines as new NET formation inhibitors. This compound class opens up new avenues for the study of cellular death through NET formation (NETosis) at different stages, and might inspire new medicinal chemistry programs aimed at NET-dependent diseases.
引用
收藏
页码:888 / 893
页数:6
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