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. 2019 Jul 22;9:10602. doi: 10.1038/s41598-019-46968-1

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© The Author(s) 2019

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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AIM2 deficiency protects mice from POI. Wt, NLRP3^−/−, NLRC4^−/− and AIM2^−/− mice underwent IM. Analysis was performed 24h after IM. (A) Infiltrating myeloperoxidase (MPO)⁺ cells were counted in ME whole mount specimens. (n_wt = 6, n_NLRP3^−/− = 5, n_NLRC4^−/− = 6, n_AIM2^−/− = 9). (B) In vivo gastrointestinal motility was analysed by detection of the geometric centre (GC). (B) (n_wt15, n_NLRP3−/− = 5, n_NLRC4−/− = 6, n_AIM2−/− = 9). (C) IL-1β production was measured in ME organ culture supernatants by ELISA. (C) (n_wt11, n_NLRP3−/− = 4, n_AIM2^−/− = 4). Statistical analyses: 1-way ANOVA with Bonferroni test. GC = geometric centre, st = stomach, c = cecum, col = colon.