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. 2018 May 21;26(2):213–228. doi: 10.1038/s41418-018-0124-5

Fig. 2.

Fig. 2

NLRP3 deficiency attenuates MPTP-induced microglial recruitment and caspase-1 activation in the SN of mouse brain. a Representative immunofluorescence image of the SN in mouse brain sections stained with anti-Iba1 antibody (red). DAPI represents the nuclear signal (blue). Scale bars, 200 μm. Magnified immunofluorescence images of the boxed areas in the middle panel are displayed in the right panel. b Quantification of relative Iba1-positive cells per DAPI in confocal images of PBS- or MPTP-treated Nlrp3+/+ or Nlrp3−/− mice (n = 4). c, d Quantification of IL-1β (c) or IL-6 (d) mRNA levels in the SN of PBS- or MPTP-treated Nlrp3+/+ or Nlrp3−/− mice. (Nlrp3+/+ mice, PBS (n = 9), MPTP (n = 9 (c) or 8 (d)); Nlrp3−/− mice, PBS (n = 7), MPTP (n = 9)). e Representative immunofluorescence image of brain sections containing SN stained with FLICA. DAPI represents the nuclear signal. Scale bars, 200 μm. f Representative immunofluorescence image of substantia nigra pars reticulata (SNr) regions of PBS- or MPTP-treated Nlrp3+/+ or Nlrp3−/− mice stained with anti-ASC antibody (green). DAPI represents the nuclear signal. Scale bars (white), 50 μm. Enlarged immunofluorescence images of SNr regions of MPTP-treated Nlrp3+/+ mice were displayed in the right panel. Scale bars (red), 10 μm. Red arrows indicate ASC specks. Data were expressed as the mean ± SEM. Asterisks indicate significant differences (**P < 0.01, ***P < 0.001, n.s. not significant)