The role of extracellular vesicle fusion with target cells in triggering systemic inflammation.
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61383082%3A_____%2F24%3A00001424" target="_blank" >RIV/61383082:_____/24:00001424 - isvavai.cz</a>
Alternative codes found
RIV/00216208:11110/24:10478730
Result on the web
<a href="https://pubmed.ncbi.nlm.nih.gov/38326335/" target="_blank" >https://pubmed.ncbi.nlm.nih.gov/38326335/</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1038/s41467-024-45125-1" target="_blank" >10.1038/s41467-024-45125-1</a>
Alternative languages
Result language
angličtina
Original language name
The role of extracellular vesicle fusion with target cells in triggering systemic inflammation.
Original language description
Extracellular vesicles (EVs) play a crucial role in intercellular communication by transferring bioactive molecules from donor to recipient cells. As a result, EV fusion leads to the modulation of cellular functions and has an impact on both physiological and pathological processes in the recipient cell. This study explores the impact of EV fusion on cellular responses to inflammatory signaling. Our findings reveal that fusion renders non-responsive cells susceptible to inflammatory signaling, as evidenced by increased NF-κB activation and the release of inflammatory mediators. Syntaxin-binding protein 1 is essential for the merge and activation of intracellular signaling. Subsequent analysis show that EVs transfer their functionally active receptors to target cells, making them prone to an otherwise unresponsive state. EVs in complex with their agonist, require no further stimulation of the target cells to trigger mobilization of NF-κB. While receptor antagonists were unable to inhibit NF-κB activation, blocking of the fusion between EVs and their target cells with heparin mitigated inflammation in mice challenged with EVs.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
30502 - Other medical science
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2024
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Nature Communications
ISSN
2041-1723
e-ISSN
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Volume of the periodical
15
Issue of the periodical within the volume
1
Country of publishing house
DE - GERMANY
Number of pages
17
Pages from-to
1-17
UT code for WoS article
001159313700009
EID of the result in the Scopus database
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