1. Academic Validation
  2. Role of corin in trophoblast invasion and uterine spiral artery remodelling in pregnancy

Role of corin in trophoblast invasion and uterine spiral artery remodelling in pregnancy

  • Nature. 2012 Mar 21;484(7393):246-50. doi: 10.1038/nature10897.
Yujie Cui 1 Wei Wang Ningzheng Dong Jinglei Lou Dinesh Kumar Srinivasan Weiwei Cheng Xiaoyi Huang Meng Liu Chaodong Fang Jianhao Peng Shenghan Chen Shannon Wu Zhenzhen Liu Liang Dong Yiqing Zhou Qingyu Wu
Affiliations

Affiliation

  • 1 Molecular Cardiology, Nephrology and Hypertension, Lerner Research Institute, Cleveland Clinic, 9500 Euclid Avenue, Cleveland, Ohio 44195, USA.
Abstract

In pregnancy, trophoblast invasion and uterine spiral artery remodelling are important for lowering maternal vascular resistance and increasing uteroplacental blood flow. Impaired spiral artery remodelling has been implicated in pre-eclampsia, a major complication of pregnancy, for a long time but the underlying mechanisms remain unclear. Corin (also known as atrial natriuretic peptide-converting Enzyme) is a cardiac Protease that activates atrial natriuretic peptide (ANP), a cardiac hormone that is important in regulating blood pressure. Unexpectedly, corin expression was detected in the pregnant uterus. Here we identify a new function of corin and ANP in promoting trophoblast invasion and spiral artery remodelling. We show that pregnant corin- or ANP-deficient mice developed high blood pressure and proteinuria, characteristics of pre-eclampsia. In these mice, trophoblast invasion and uterine spiral artery remodelling were markedly impaired. Consistent with this, the ANP potently stimulated human trophoblasts in invading Matrigels. In patients with pre-eclampsia, uterine Corin messenger RNA and protein levels were significantly lower than that in normal pregnancies. Moreover, we have identified Corin gene mutations in pre-eclamptic patients, which decreased corin activity in processing pro-ANP. These results indicate that corin and ANP are essential for physiological changes at the maternal-fetal interface, suggesting that defects in corin and ANP function may contribute to pre-eclampsia.

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