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. 2019 Jun 11;9:8480. doi: 10.1038/s41598-019-44854-4

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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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NLRP12 inhibition regulates cellular proliferation. (a) NLRP12 expression was observed in glioma (LN18) and microglial (BV2) cells using immunofluorescence (magnification: 40X, scale bar: 50 μm). (b) Colony formation assay shows increased cellular proliferation in the NLRP12si treated microglia. Magnification: 40X. (c,d) Quantification of both BV2 and LN18 cells per colony. (e) Effect of LN18 (NLRP12 siRNA treated) cell conditioned medium (CM) on BV2 cell migration was assessed using migration assay. 8 image sections per sample were quantified for migration analysis. Student’s t-test and one-way AVOVA were performed to find the statistical significance of colony formation and migration assay respectively (p-value; *<0.05, **<0.005). The error bar indicates standard error of mean. (f) NLRP12 expression in human normal brain tissue and glioma sections, using anti-NLRP12 antibody (N = 7). Nuclei were stained blue with DAPI and microglia were stained green with FITC tagged lectin RCA (Ricinus Communis Agglutinin-1); Magnification: 20X, scale bar: 100 µm.