Journal: Nature Communications
Article Title: Suppression of TGF-β/SMAD signaling by an inner nuclear membrane phosphatase complex
doi: 10.1038/s41467-025-58681-x
Figure Lengend Snippet: A Localization of endogenous SMAD2 in HeLa parental cells or lacking the indicated genes analyzed by immunofluorescence. DNA was labeled with 4′,6- diamidino- 2- phenylindole (DAPI). Scale bar: 10 μM. B Quantification of nuclear accumulation of SMAD2 from imaging experiments, as shown in ( A ), n = 3 independent experiments, p -values were indicated in the graph. One-way ANOVA (multiple comparison) was performed, and data are presented as mean values ± SD. C Levels of endogenous pSMAD2 and SMAD2 in HeLa parental cells or lacking the indicated genes. Cell lysates were analyzed by SDS-PAGE followed by immunoblotting with the indicated antibodies. GAPDH was used as a loading control. D Levels of endogenous pSMAD2 and SMAD2 in HeLa parental cells or CTDENP1 KO cells with indicated treatments. The 1D11 antibody against TGF-β cytokine was used at 30, 150, and 300 µg/mL; mouse IgG antibody was used at 300 µg/mL; the TGF-β receptor specific inhibitor SB431542 was used at 10 µM. Cell lysates were analyzed by SDS-PAGE followed by immunoblotting with the indicated antibodies. GAPDH was used as a loading control. E levels of p21, p15 transcripts in HeLa parental cells or lacking the indicated genes analyzed by RT-qPCR. n = 3 independent experiments, each with 3 technical replicates. p -values were indicated in the graph. One-way ANOVA (multiple comparison) was performed, and data are presented as mean values ± SD. F levels of endogenous p21 in HeLa parental cells or lacking the indicated genes. Cell lysates were analyzed by SDS-PAGE followed by immunoblotting with the indicated antibodies. GAPDH was used as a loading control. G Quantification of S phase cells assessed based on EdU incorporation and DAPI staining. At least 30000 cells were analyzed for each condition. n = 3 independent experiments, p -values were indicated in the graph. One-way ANOVA (multiple comparison) was performed, and data are presented as mean values ± SD. H The CTDNEP1-NEP1R1-MAN1 complex dephosphorylates and inactivates R-SMADs at the INM (see text for details).
Article Snippet: Inhibition of TGF-β ligands was performed with the neutralizing antibody, 1D11 (BioX-Cell # #BE0083), and isotype-matched IgG1 monoclonal control antibody (BioX-Cell #BE0057) were used at 30, 150, and 300 μg/mL, respectively, to treat HeLa parental cells or CTDENP1 KO cells with indicated time.
Techniques: Immunofluorescence, Labeling, Imaging, Comparison, SDS Page, Western Blot, Control, Quantitative RT-PCR, Staining
