| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1928753 | Biochemical and Biophysical Research Communications | 2013 | 7 Pages |
Members of the KLFs family of transcription factors play roles in maternal endometrium development during embryo implantation. However, the specific role of KLF12 in endometrium development has not yet been described. In this study, we showed that KLF12 expression in human endometrial stromal cells (HESCs) was significantly decreased after decidualization stimulated by 8-Br-cAMP and medroxyprogesterone acetate (MPA). The adenovirus-mediated overexpression of KLF12 in HESCs significantly repressed the expression and secretion of decidualization biomarker genes and their products decidual prolactin (PRL) and insulin-like growth factor binding protein-1 (IGFBP-1) induced by 8-Br-cAMP and MPA. Moreover, CHIP and luciferase reporter assays demonstrated that KLF12 bound to a CAGTGGG element within the decidual prolactin promoter and decreased decidual PRL promoter (dPRL/-2000Luc) activation in a sequence-specific manner. Taken together, these findings suggest KLF12 is a negative regulator of human endometrial stromal cell decidualization.
► KLF12 repressed the expression and secretion of PRL and IGFBP-1 induced by 8-Br-cAMP and MPA. ► KLF12 decreased decidual PRL promoter activation in a sequence-specific manner. ► KLF12 is a negative regulator of human endometrial stromal cell decidualization.
