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Status: Bibliographieeintrag

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Verfasst von:Robichon, Katharina [VerfasserIn]   i
 Maiwald, Tim [VerfasserIn]   i
 Schilling, Marcel [VerfasserIn]   i
 Kopp-Schneider, Annette [VerfasserIn]   i
 Willemsen, Joschka [VerfasserIn]   i
 Salopiata, Florian [VerfasserIn]   i
 Teusel, Melissa [VerfasserIn]   i
 Kreutz, Clemens [VerfasserIn]   i
 Ehlting, Christian [VerfasserIn]   i
 Huang, Jun [VerfasserIn]   i
 Chakraborty, Sajib [VerfasserIn]   i
 Huang, Xiaoyun [VerfasserIn]   i
 Damm, Georg [VerfasserIn]   i
 Seehofer, Daniel [VerfasserIn]   i
 Lang, Philipp A. [VerfasserIn]   i
 Bode, Johannes G. [VerfasserIn]   i
 Binder, Marco [VerfasserIn]   i
 Bartenschlager, Ralf [VerfasserIn]   i
 Timmer, Jens [VerfasserIn]   i
 Klingmüller, Ursula [VerfasserIn]   i
Titel:Identification of interleukin1β as an amplifier of interferon alpha-induced antiviral responses
Verf.angabe:Katharina Robichon, Tim Maiwald, Marcel Schilling, Annette Schneider, Joschka Willemsen, Florian Salopiata, Melissa Teusel, Clemens Kreutz, Christian Ehlting, Jun Huang, Sajib Chakraborty, Xiaoyun Huang, Georg Damm, Daniel Seehofer, Philipp A. Lang, Johannes G. Bode, Marco Binder, Ralf Bartenschlager, Jens Timmer, Ursula Klingmüller
E-Jahr:2020
Jahr:October 1, 2020
Fussnoten:Gesehen am 12.11.2020
Titel Quelle:Enthalten in: Public Library of SciencePLoS pathogens
Ort Quelle:Lawrence, Kan. : PLoS, 2005
Jahr Quelle:2020
Band/Heft Quelle:16(2020,10) Artikel-Nummer e1008461, 33 Seiten
ISSN Quelle:1553-7374
Abstract:The induction of an interferon-mediated response is the first line of defense against pathogens such as viruses. Yet, the dynamics and extent of interferon alpha (IFNα)-induced antiviral genes vary remarkably and comprise three expression clusters: early, intermediate and late. By mathematical modeling based on time-resolved quantitative data, we identified mRNA stability as well as a negative regulatory loop as key mechanisms endogenously controlling the expression dynamics of IFNα-induced antiviral genes in hepatocytes. Guided by the mathematical model, we uncovered that this regulatory loop is mediated by the transcription factor IRF2 and showed that knock-down of IRF2 results in enhanced expression of early, intermediate and late IFNα-induced antiviral genes. Co-stimulation experiments with different pro-inflammatory cytokines revealed that this amplified expression dynamics of the early, intermediate and late IFNα-induced antiviral genes can also be achieved by co-application of IFNα and interleukin1 beta (IL1β). Consistently, we found that IL1β enhances IFNα-mediated repression of viral replication. Conversely, we observed that in IL1β receptor knock-out mice replication of viruses sensitive to IFNα is increased. Thus, IL1β is capable to potentiate IFNα-induced antiviral responses and could be exploited to improve antiviral therapies.
DOI:doi:10.1371/journal.ppat.1008461
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1371/journal.ppat.1008461
 Volltext: https://journals.plos.org/plospathogens/article?id=10.1371/journal.ppat.1008461
 DOI: https://doi.org/10.1371/journal.ppat.1008461
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Antiviral therapy
 Gene expression
 Gene regulation
 Hepatocytes
 Messenger RNA
 Phosphorylation
 Small interfering RNA
 Viral gene expression
K10plus-PPN:1738573249
Verknüpfungen:→ Zeitschrift

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