Neither microcystin, nor nodularin, nor cylindrospermopsin directly interact with human toll-like receptors
Jazyk angličtina Země Anglie, Velká Británie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
33515847
DOI
10.1016/j.chemosphere.2021.129623
PII: S0045-6535(21)00092-8
Knihovny.cz E-zdroje
- Klíčová slova
- Cyanotoxin, Inflammation, NF-κB, Toll-like receptor,
- MeSH
- alkaloidy MeSH
- cyklické peptidy MeSH
- HEK293 buňky MeSH
- lidé MeSH
- mikrocystiny * toxicita MeSH
- tandemová hmotnostní spektrometrie * MeSH
- toll-like receptory genetika MeSH
- toxiny kmene Cyanobacteria MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- alkaloidy MeSH
- cyklické peptidy MeSH
- cylindrospermopsin MeSH Prohlížeč
- mikrocystiny * MeSH
- nodularin MeSH Prohlížeč
- toll-like receptory MeSH
- toxiny kmene Cyanobacteria MeSH
Various stressors including temperature, environmental chemicals, and toxins can have profound impacts on immunity to pathogens. Increased eutrophication near rivers and lakes coupled with climate change are predicted to lead to increased algal blooms. Currently, the effects of cyanobacterial toxins on disease resistance in mammals is a largely unexplored area of research. Recent studies have suggested that freshwater cyanotoxins can elicit immunomodulation through interaction with specific components of innate immunity, thus potentially altering disease susceptibility parameters for fish, wildlife, and human health owing to the conserved nature of the vertebrate immune system. In this study, we investigated the effects of three microcystin congeners (LR, LA, and RR), nodularin-R, and cylindrospermopsin for their ability to directly interact with nine different human Toll-like receptors (TLRs)-key pathogen recognition receptors for innate immunity. Toxin concentrations were verified by LC/MS/MS prior to use. Using an established HEK293-hTLR NF-κB reporter assay, we concluded that none of the tested toxins (29-90 nM final concentration) directly interacted with human TLRs in either an agonistic or antagonistic manner. These results suggest that earlier reports of cyanotoxin-induced NF-κB responses likely occur through different surface receptors to mediate inflammation.
U S Geological Survey Kansas Water Science Center 1217 Biltmore Dr Lawrence KS 66049 USA
U S Geological Survey Western Fisheries Research Center 6505 NE 65th St Seattle WA 98115 USA
Citace poskytuje Crossref.org