Role of TRAF6 adaptor in the immune responses to murine polyomavirus
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F23%3A10464745" target="_blank" >RIV/00216208:11310/23:10464745 - isvavai.cz</a>
Výsledek na webu
<a href="https://innate-immunity-conference.de/programme/scientific-programme" target="_blank" >https://innate-immunity-conference.de/programme/scientific-programme</a>
DOI - Digital Object Identifier
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Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Role of TRAF6 adaptor in the immune responses to murine polyomavirus
Popis výsledku v původním jazyce
Polyomaviruses are associated with many diseases due to their ability to persistently infect the host. Since 2008, twelve new human polyomaviruses have been discovered. Among the new species, Merkel cell polyomavirus (MCPyV) was identified as the etiological agent of skin Merkel cell carcinoma. Unfortunately, the cell type productively infected by MCPyV is unknown and therefore in vitro studies of the MCPyV are still a challenge. Nevertheless, its closest related member, Murine polyomavirus (MPyV) has been used per decades as in vitro model to understand fundamental questions about the biology of polyomaviruses. We demonstrated that MPyV activates innate immunite responses via GAS-STING and TLR4. It is known that the transcription factors, NF-Ƙβ and IRF3 are activated during launching of the above pathways. However, NF-Ƙβ is mainly activated by TLR4 for pro-inflammatory cytokines production and IRF3 by cGAS-STING for interferon (IFN) production.
Název v anglickém jazyce
Role of TRAF6 adaptor in the immune responses to murine polyomavirus
Popis výsledku anglicky
Polyomaviruses are associated with many diseases due to their ability to persistently infect the host. Since 2008, twelve new human polyomaviruses have been discovered. Among the new species, Merkel cell polyomavirus (MCPyV) was identified as the etiological agent of skin Merkel cell carcinoma. Unfortunately, the cell type productively infected by MCPyV is unknown and therefore in vitro studies of the MCPyV are still a challenge. Nevertheless, its closest related member, Murine polyomavirus (MPyV) has been used per decades as in vitro model to understand fundamental questions about the biology of polyomaviruses. We demonstrated that MPyV activates innate immunite responses via GAS-STING and TLR4. It is known that the transcription factors, NF-Ƙβ and IRF3 are activated during launching of the above pathways. However, NF-Ƙβ is mainly activated by TLR4 for pro-inflammatory cytokines production and IRF3 by cGAS-STING for interferon (IFN) production.
Klasifikace
Druh
O - Ostatní výsledky
CEP obor
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OECD FORD obor
10607 - Virology
Návaznosti výsledku
Projekt
<a href="/cs/project/LX22NPO5103" target="_blank" >LX22NPO5103: Národní institut virologie a bakteriologie</a><br>
Návaznosti
P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)
Ostatní
Rok uplatnění
2023
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů