ppat.1006829.g004.tif (158.06 kB)
L. pneumophila infection and stimulation with DNA or cGAMP induce weak cGAS-dependent type I IFN responses in THP-1 cells.
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posted on 2018-01-03, 18:40 authored by Juan S. Ruiz-Moreno, Lutz Hamann, Javeed A. Shah, Annelies Verbon, Frank P. Mockenhaupt, Monika Puzianowska-Kuznicka, Jan Naujoks, Leif E. Sander, Martin Witzenrath, John C. Cambier, Norbert Suttorp, Ralf R. Schumann, Lei Jin, Thomas R. Hawn, Bastian OpitzWT THP-1 or cGAS-/- THP-1 clones A5 and B5 were allowed differentiation prior to stimulation with either cGAMP or synthetic DNA (A) or infection with two different strains of L. pneumophila (B). IFNB expression was determined by qRT-PCR. Data represent mean ± SEM of 2 independent experiments carried out in duplicates. Analyses were performed by employing the Mann-Whitney U Test. Comparisons with a p < 0.05 were considered significant.
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R 232H attenuated cytokine productionsusceptibilitySTING-deficient murine macrophagesR 232H allelescyclic GMP-AMP synthaseSTING-deficient animalscyclic dinucleotidesTMEMIFNprotozoal infectionsRecent studiesHAQ STING variant impairs cGAS-dependentcGAS-STING cascadeLegionnairehaplotype frequencyDNATrial registration ClinicalTrials.gov DRKS 00005274CDNmouse modelwild-type miceLegionella pneumophilaresponsepro-inflammatory cytokines
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