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. 2016 Jun 15;12(6):e1005716. doi: 10.1371/journal.ppat.1005716

Correction: Macrophage-expressed IFN-β Contributes to Apoptotic Alveolar Epithelial Cell Injury in Severe Influenza Virus Pneumonia

Katrin Högner, Thorsten Wolff, Stephan Pleschka, Stephanie Plog, Achim D Gruber, Ulrich Kalinke, Hans-Dieter Walmrath, Johannes Bodner, Stefan Gattenlöhner, Peter Lewe-Schlosser, Mikhail Matrosovich, Werner Seeger, Juergen Lohmeyer, Susanne Herold
PMCID: PMC4909187  PMID: 27304804

The authors would like to correct Fig 8D, as errors were introduced in the preparation of the figure for publication. In the right panel of Fig 8D, the ifnar-/- plot is incorrect, a pkr-/- plot was used in place of the correct ifnar-/- plot. The corrected Fig 8, shown here, includes the correct infar-/- plot.

Fig 8. Blockade of autocrine myeloid IFN-β signalling impairs macrophage TRAIL expression and attenuates epithelial injury upon A/PR8 infection in vivo.

Fig 8

(A) Treatment protocol: CD45.1+ wt mice were lethally irradiated (6 Gy) and transplanted 1×106 CD45.2+ wt, pkr −/−, ifnar −/− or trail −/− BM cells to generate chimeric mice. 12w later, when >90% of AM were of donor (wt, pkr −/−, ifnar −/− or trail −/−) phenotype, chimeric mice were mock- or A/PR8-infected and subjected to analyses at 2 d or 7 d pi. (B, C) depict IV-induced sTRAIL concentrations in BALF (B) and proportions of mTRAIL-expressing AM and ExMac (exudate macrophages) in BALF of chimeric mice at d2 pi (C). (D, E) AEC apoptosis was quantified in mock- or A/PR8-infected chimeric mice at d7 pi by FACS (D, depicted as Annexin V+ proportion of CD31CD45EpCam+lung cells, left panel; representative FACS plots, right panel) or by western blot using lysates of AEC isolated from mock- or A/PR8-infected chimeric mice and a cleaved caspase-3-specific Ab (E, top panel, western blot of 3 independent experiments; bottom panel, quantification of western blot data by densitometry). (F) Alveolar albumin leakage was analysed in mock- or A/PR8-infected wt and trail −/ chimeric mice at d7 pi by intravenous injection of FITC-labelled albumin and is depicted as ratio of serum and BALF FITC-fluorescence in arbitrary units (AU). (G) Body weight of wt and trail −/chimeric mice was determined post A/PR8 infection (350 pfu/∼30%LD50). Bar graphs show means ± SD of (B, C, D, E, F) 5 animals/group and (G) 8 animals/group. * p<0,05; ** p<0,01; ***p<0,001; n.d.; not determined; BMT, bone marrow transplantation; dpi, days post infection; pi, post infection; sTRAIL, soluble TRAIL; mTRAIL, membrane bound TRAIL; Ab, antibody.

The authors confirm that these changes do not alter their findings.

Reference


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