Journal: European Journal of Medical Research
Article Title: Epigenetic regulation by WTAPP1 promotes trophoblast dysfunction in gestational diabetes via CNR1/NF-κB activation
doi: 10.1186/s40001-025-03217-8
Figure Lengend Snippet: WTAPP1 promoted CNR1 expression in an m6A-dependent manner. A Bioinformatics prediction of m6A enrichment in CNR1 mRNA sequence. B m6A enrichment levels of CNR1 mRNA in placental samples of GDM and NC group and in WTAPP1-knockdown cells treated with NG or HG (fold: relative to NC or NG group). C RT-qPCR analysis of WTAP mRNA expression in placental samples of GDM and NC group and in WTAPP1-knockdown cells treated with NG or HG (fold: relative to NC or NG group). D Western blot detection of WTAP protein levels in placental samples of GDM and NC group and in WTAPP1-knockdown cells treated with NG or HG. Cells were transfected with WTAPP1 overexpression vectors (oeWP1) and WTAP knockdown vectors (oeWP1/kdW). E The gene expression of WTAP1 and CNR1 was analyzed in cells (fold: relative to NC group). F The m6A enrichment of CNR1 mRNA (fold: relative to NC group). G The mRNA remaining of CNR1 in cells treated by actinomycin D (fold: relative to 0 h). H-I The protein expression of CNR1, p-IkBα, IkBα, p-p65, and p65. J, The protein expression of nuclear p65. ns P > 0.05, * P < 0.05, ** P < 0.01, and *** P < 0.001
Article Snippet: CNR1 , Rabbit , Proteintech , 17978-1-AP , 1:2000.
Techniques: Expressing, Sequencing, Knockdown, Quantitative RT-PCR, Western Blot, Transfection, Over Expression, Gene Expression