Early inflammatory profiling of schwannoma cells induced by lipopolysaccharide
Jazyk angličtina Země Německo Médium print-electronic
Typ dokumentu časopisecké články
Grantová podpora
16-08508S
The Czech Science Foundation
LO1214
the National Sustainability Programme of the Czech Ministry of Education, Youth and Sports
LM2015051
the RECETOX research infrastructure
PubMed
28755317
DOI
10.1007/s00418-017-1601-5
PII: 10.1007/s00418-017-1601-5
Knihovny.cz E-zdroje
- Klíčová slova
- Cytokines, Early endosomes, Schwann cells, Toll-like receptor 4, Transforming factors,
- MeSH
- krysa rodu Rattus MeSH
- ligandy MeSH
- lipopolysacharidy farmakologie MeSH
- nádorové buňky kultivované MeSH
- neurilemom metabolismus patologie MeSH
- toll-like receptor 4 antagonisté a inhibitory metabolismus MeSH
- zánět metabolismus MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- ligandy MeSH
- lipopolysacharidy MeSH
- Tlr4 protein, rat MeSH Prohlížeč
- toll-like receptor 4 MeSH
Inflammatory profiling of Schwann cells manifested as an upregulation of cytokines is present after traumatic or disease injury of the peripheral nerves. Inflammatory activation of Schwann cells via Toll-like receptors (TLRs) can be triggered by exogenous pathological molecules or endogenous ligands produced during Wallerian degeneration. We investigated the early period of inflammatory reactions by following the levels of TLR4, NFκB, IL-1β, pSTAT3, and IL-6 proteins after LPS treatment of RT4 schwannoma cells under in vitro conditions. Significantly increased levels of NFκB, IL-1β, pSTAT3, and IL-6 proteins were found 1 h after LPS action indicating their involvement in the initiation of the inflammatory reaction of schwannoma cells. This initiation was induced without increased TLR4 protein expression, but was accompanied by the appearance of TLR4 in early endosomes. The protein levels decreased within the next 6 h of treatment with a subsequent increase of NFκB, IL-1β, and pSTAT3 after 24 h of LPS treatment. In contrast, continuous decrease of IL-6 over time following LPS treatment was unexpected. Levels of soluble IL-6 protein in the culture medium also decreased with decreasing levels of LPS over 24 h.
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