Copyright: ©Author(s) 2026.
World J Gastroenterol. Aug 14, 2026; 32(30): 119465
Published online Aug 14, 2026. doi: 10.3748/wjg.v32.i30.119465
Published online Aug 14, 2026. doi: 10.3748/wjg.v32.i30.119465
Figure 2 Successful generation of differential signal transducer and activator of transcription 3 expressing cell lines.
Signal transducer and activator of transcription 3 (STAT3) expression was modified by generation of differential, stable, lentiviral transduced Caco-2 or T84 cell lines. Reduction of STAT3 (STAT3 -) was produced via short hairpin RNA (shRNA) targeting STAT3. Enhanced STAT3 expression (STAT3 +) was induced by transduction of STAT3 expression plasmids. A non-mammalian shRNA expressing pLKO.1 vector was used as a control. Differential STAT3 expression was validated frequently from the start to the end of the experiments. Total protein was extracted, and proteins of interest were analyzed. A: Western blot; B: Quantified using Fiji (ImageJ distribution; version 2.14.0/1.54f). Values were normalized to Caco-2 or T84 control cell lines. Bars indicate mean ± SD. P values were calculated using one-way analysis of variance and post hoc Tukey analysis (n = 4). bP < 0.01. dP < 0.0001. STAT3: Signal transducer and activator of transcription 3.
- Citation: Leinz N, Beyer S, Yoganathan-Kugarajan B, Kraus N, Ortiz C, Hahnefeld L, Gurke R, Başoğlu M, Plotz G, Eimer S, Zeuzem S, Trebicka J, Welsch C, Brieger A. Dysregulated signal transducer and activator of transcription 3 drives intestinal permeability and may contribute to acute-on-chronic liver failure. World J Gastroenterol 2026; 32(30): 119465
- URL: https://www.wjgnet.com/1007-9327/full/v32/i30/119465.htm
- DOI: https://dx.doi.org/10.3748/wjg.v32.i30.119465