Correction to: Scientific Reports https://doi.org/10.1038/s41598-020-70513-0, published online 11 August 2020

This Article contains an error.

Due to an error during figure assembly Figure 3e, panel “Vehicle/LPS(-)” duplicates Figure 3c, panel “MCC950 (50 μM)/LPS (0.1 ng/mL)”. The corrected version of Figure 3 is provided below.

Fig. 3
figure 3

KN3014 reduced ASC-speck formation accompanied by IL-1β processing and secretion with no effect on pro-IL-1β production or NF-κB activation. (a) Western blotting analysis of LPS (0.1 ng/mL) induced pro-IL-1β production (upper panel) and IL-1β cleavage (middle panel; the same blotting membrane shown in the upper panel was re-hybridized with a mAb specific for cleaved-IL-1β (long exposure)). The same gel was stained with Coomassie brilliant blue (lower panel). (b) IL-1β concentrations in the supernatant of each well measured by ELISA. (c) Immunofluorescence microscopy evaluation of ASC-speck formation. (d) Percentage of ASC specks (%). (e) Immunofluorescence microscopy evaluation of NF-κB p65 nuclear translocation. (f) Relative nuclear translocation of NF-κB p65. Results are given as means ± standard deviation of three hyper views. *p-value < 0.05 (Mann–Whitney U-test). These results are representative of two independent experiments. Scale bars = 10 μm.