| Literature DB >> 28240414 |
Nancy E Martinez1,2,3, Tobias J Zimmermann1,2, Christian Goosmann3, Tobias Alexander4, Christian Hedberg5, Slava Ziegler1, Arturo Zychlinsky3, Herbert Waldmann1,2.
Abstract
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.Entities:
Keywords: NETosis; inhibitors; neutrophil extracellular traps (NETs); structure-activity relationships; tetrahydroisoquinolines
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Year: 2017 PMID: 28240414 DOI: 10.1002/cbic.201600650
Source DB: PubMed Journal: Chembiochem ISSN: 1439-4227 Impact factor: 3.164