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High hydrostatic pressure induces immunogenic cell death in human tumor cells
J. Fucikova, I. Moserova, I. Truxova, I. Hermanova, I. Vancurova, S. Partlova, A. Fialova, L. Sojka, PF. Cartron, M. Houska, L. Rob, J. Bartunkova, R. Spisek,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
Grantová podpora
NT11559
MZ0
CEP - Centrální evidence projektů
NT12402
MZ0
CEP - Centrální evidence projektů
PubMed
24500981
DOI
10.1002/ijc.28766
Knihovny.cz E-zdroje
- MeSH
- adenosintrifosfát sekrece MeSH
- aktivace enzymů imunologie MeSH
- antigeny CD86 biosyntéza MeSH
- apoptóza imunologie MeSH
- CD antigeny biosyntéza MeSH
- dendritické buňky imunologie MeSH
- eukaryotický iniciační faktor 2 metabolismus MeSH
- fagocytóza imunologie MeSH
- fosforylace MeSH
- HLA-DR antigeny biosyntéza MeSH
- hydrostatický tlak MeSH
- imunoglobuliny biosyntéza MeSH
- interleukin-12 sekrece MeSH
- interleukin-6 sekrece MeSH
- kalretikulin biosyntéza imunologie MeSH
- kaspasa 8 metabolismus MeSH
- lidé MeSH
- membránové glykoproteiny biosyntéza MeSH
- membránové proteiny biosyntéza MeSH
- nádorové buněčné linie MeSH
- nádory imunologie MeSH
- protein HMGB1 imunologie sekrece MeSH
- proteiny tepelného šoku HSP70 biosyntéza imunologie MeSH
- proteiny tepelného šoku HSP90 biosyntéza imunologie MeSH
- reaktivní formy kyslíku metabolismus MeSH
- regulační T-lymfocyty imunologie MeSH
- stres endoplazmatického retikula imunologie MeSH
- TNF-alfa sekrece MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Recent studies have identified molecular events characteristic of immunogenic cell death (ICD), including surface exposure of calreticulin (CRT), the heat shock proteins HSP70 and HSP90, the release of high-mobility group box protein 1 (HMGB1) and the release of ATP from dying cells. We investigated the potential of high hydrostatic pressure (HHP) to induce ICD in human tumor cells. HHP induced the rapid expression of HSP70, HSP90 and CRT on the cell surface. HHP also induced the release of HMGB1 and ATP. The interaction of dendritic cells (DCs) with HHP-treated tumor cells led to a more rapid rate of DC phagocytosis, upregulation of CD83, CD86 and HLA-DR and the release of interleukin IL-6, IL-12p70 and TNF-α. DCs pulsed with tumor cells killed by HHP induced high numbers of tumor-specific T cells. DCs pulsed with HHP-treated tumor cells also induced the lowest number of regulatory T cells. In addition, we found that the key features of the endoplasmic reticulum stress-mediated apoptotic pathway, such as reactive oxygen species production, phosphorylation of the translation initiation factor eIF2α and activation of caspase-8, were activated by HHP treatment. Therefore, HHP acts as a reliable and potent inducer of ICD in human tumor cells.
Citace poskytuje Crossref.org
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- $a Recent studies have identified molecular events characteristic of immunogenic cell death (ICD), including surface exposure of calreticulin (CRT), the heat shock proteins HSP70 and HSP90, the release of high-mobility group box protein 1 (HMGB1) and the release of ATP from dying cells. We investigated the potential of high hydrostatic pressure (HHP) to induce ICD in human tumor cells. HHP induced the rapid expression of HSP70, HSP90 and CRT on the cell surface. HHP also induced the release of HMGB1 and ATP. The interaction of dendritic cells (DCs) with HHP-treated tumor cells led to a more rapid rate of DC phagocytosis, upregulation of CD83, CD86 and HLA-DR and the release of interleukin IL-6, IL-12p70 and TNF-α. DCs pulsed with tumor cells killed by HHP induced high numbers of tumor-specific T cells. DCs pulsed with HHP-treated tumor cells also induced the lowest number of regulatory T cells. In addition, we found that the key features of the endoplasmic reticulum stress-mediated apoptotic pathway, such as reactive oxygen species production, phosphorylation of the translation initiation factor eIF2α and activation of caspase-8, were activated by HHP treatment. Therefore, HHP acts as a reliable and potent inducer of ICD in human tumor cells.
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