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. Author manuscript; available in PMC: 2010 May 1.
Published in final edited form as: Nature. 2009 Jan 21;458(7237):509–513. doi: 10.1038/nature07710

Figure 3. Cell-based reconstitution of the AIM2 inflammasome.

Figure 3

a, Percentages of ASC pyroptosomes in untransfected (none) or poly (dA:dT)-transfected THP-1 cells. Values represent mean and s.d. (n = 3). b, Fluorescence confocal images showing formation of the speck-like ASC pyroptosomes only in 293-AIM2-ASC-EGFP-N1 cells (right panels), but not in 293-ASC-EGFP-N1 cells (left panels), 2 h after transfection with vehicle (control, upper panels) or poly (dA:dT) (lower panels). DIC, Differential Interference Contrast. c, Percentages of ASC pyroptosomes in the indicated cell lines following transfection with poly (dA:dT) for 2h. Values represent mean ± S.D. (n = 7); *, P<0.005; **, P<0.001. d, Immunoblot for caspase-1 in lysates from 293-caspase-1-ASC (1st to 5th lanes) or 293-caspase-1-ASC-AIM2 (6th to 10th lanes) cells following transfection with the indicated types of DNA (0.5 µg/1 × 106 cells) for 24 h. e, Immunoblot for AIM2 (upper panel) or Omi (lower panel) in lysates from uninduced (1st lane) or interferon γ-induced (2nd lane) THP-1 cells, or 293-caspase-1-ASC-AIM2 cells (3rd lane). f, Immunoblot for caspase-1 in lysates from 293-caspase-1-ASC (1st to 4th lanes) or 293-caspase-1-ASC-NALP3 (5th to 8th lanes) cells following transfection with the indicated plasmid DNA (0.5 µg /1 × 106 cells) for 24 h.