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. 2023 Mar 7;14:1117285. doi: 10.3389/fmicb.2023.1117285

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Copyright © 2023 Wang, Liu, Zhang, Yu and Ai.

This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

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Effect of MALT1 on cell apoptosis in multiple organs of LPS-induced septic mouse model. TUNEL assay of lung, liver, and kidney tissues among the Model, LV-NC, LV-MALT1, and LV-shMALT1 groups (A). Comparison of the TUNEL-positive rate of the lung (B), liver (C), and kidney (D) among the Model, LV-NC, LV-MALT1, and LV-shMALT1 groups. IHC analysis of cleaved-caspase3 in lung, liver, and kidney tissues among the Model, LV-NC, LV-MALT1, and LV-shMALT1 groups (E). Comparison of cleaved-caspase3 IHC scores of the lung (F), liver (G), and kidney (H) among the Model, LV-NC, LV-MALT1, and LV-shMALT1 groups. n = 6 in each group. One-way ANOVA plus Tukey’s post hoc test was applied. Ns, not significant; *p < 0.05; **p < 0.01.