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. 2016 Jul 15;27(14):2186–2197. doi: 10.1091/mbc.E16-02-0086

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© 2016 Forteza et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0).

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FIGURE 9: — Cytokine mRNA expression from isolated small intestine enterocytes from Prkci^flox/flox Vil-CRE± (KO). Each data set comprises mRNAs from two different groups of animals for control littermates (lm) and KO, except for CXCL-1, which also comprises animals treated with oral SS or intraperitoneal Y27628. For each group, values were normalized to one control animal (lm). Horizontal lines represent average. Vimentin and IL-1β mRNA were measured in preparations of isolated enterocytes (E) or spleen (S) from the same animals to assess connective tissue contamination of the epithelium preparations. Kruskal–Wallis test, H₀ = control lm and KO populations are equal, p < 0.005 (CXCL-1), p < 0.05 (CXCL-2), p < 0.05 (IL-1α), SS or Y27628 groups, not significant. For vimentin and IL-1b, H₀ = spleen data are equal to enterocytes, p < 0.001.