1. Krüppel-like factor 17 upregulates uterine corin expression and promotes spiral artery remodeling in pregnancy
- Author
-
Shengnan Zhang, Ningzheng Dong, Shengxuan Sun, Qingyu Wu, Yayan Niu, Can Wang, Zhiting Wang, Hui Li, Meng Liu, Ying Xu, Tiantian Zhou, Meiling He, and Ce Zhang
- Subjects
Gestational hypertension ,Male ,Spiral artery ,Vascular Remodeling ,Preeclampsia ,Andrology ,Mice ,Krüppel ,Pregnancy ,medicine ,Animals ,Humans ,Promoter Regions, Genetic ,Transcription factor ,Cells, Cultured ,Mice, Knockout ,Fetus ,Multidisciplinary ,business.industry ,Serine Endopeptidases ,Uterus ,Arteries ,Hypertension, Pregnancy-Induced ,Biological Sciences ,medicine.disease ,Transmembrane protein ,Proteinuria ,Fertility ,Gene Expression Regulation ,Female ,business ,Transcription Factors - Abstract
Spiral artery remodeling is an important physiological process in the pregnant uterus which increases blood flow to the fetus. Impaired spiral artery remodeling contributes to preeclampsia, a major disease in pregnancy. Corin, a transmembrane serine protease, is up-regulated in the pregnant uterus to promote spiral artery remodeling. To date, the mechanism underlying uterine corin up-regulation remains unknown. Here we show that Kruppel-like factor (KLF) 17 is a key transcription factor for uterine corin expression in pregnancy. In cultured human uterine endometrial cells, KLF17 binds to the CORIN promoter and enhances the promoter activity. Disruption of the KLF17 gene in the endometrial cells abolishes CORIN expression. In mice, Klf17 is up-regulated in the pregnant uterus. Klf17 deficiency prevents uterine Corin expression in pregnancy. Moreover, Klf17-deficient mice have poorly remodeled uterine spiral arteries and develop gestational hypertension and proteinuria. Together, our results reveal an important function of KLF17 in regulating Corin expression and uterine physiology in pregnancy.
- Published
- 2020