Specific HIF-2α (Hypoxia-Inducible Factor-2) Inhibitor PT2385 Mitigates Placental Dysfunction In Vitro and in a Rat Model of Preeclampsia (RUPP)

Author:

Colson Arthur123ORCID,Depoix Christophe Louis1ORCID,Lambert Isaline1,Leducq Camille1,Bedin Marie2,De Beukelaer Michèle4,Gatto Laurent5ORCID,Loriot Axelle5,Peers de Nieuwburgh Maureen1,Bouhna Khadija13,Baldin Pamela6,Hubinont Corinne13,Sonveaux Pierre27,Debiève Frédéric13

Affiliation:

1. Pôle de Recherche en Physiopathologie de la Reproduction, Institut de Recherche Expérimentale et Clinique (A.C., C.L.D., I.L., C.L., M.P.d.N., K.B., C.H., F.D.), Université catholique de Louvain, Brussels, Belgium.

2. Pôle de Recherche en Pharmacothérapie, Institut de Recherche Expérimentale et Clinique (A.C., M.B., P.S.), Université catholique de Louvain, Brussels, Belgium.

3. Department of Obstetrics (A.C., K.B., C.H., F.D.), Cliniques universitaires Saint-Luc, Brussels, Belgium.

4. Imaging Core Facility 2IP, Institut de Recherche Expérimentale et Clinique (M.D.B.), Université catholique de Louvain, Brussels, Belgium.

5. Unit of Computational Biology and Bioinformatics, de Duve Institute (L.G., A.L.), Université catholique de Louvain, Brussels, Belgium.

6. Department of Pathology (P.B.), Cliniques universitaires Saint-Luc, Brussels, Belgium.

7. Walloon Excellence in Life Sciences and Biotechnology Research Institute, Wavre, Belgium (P.S.).

Abstract

Background: Preeclampsia is one of the leading causes of maternal mortality worldwide and is strongly associated with long-term morbidity in mothers and newborns. Referred to as one of the deep placentation disorders, insufficient remodeling of the spiral arteries during the first trimester remains a major cause of placental dysfunction. Persisting pulsatile uterine blood flow causes abnormal ischemia/reoxygenation phenomenon in the placenta and stabilizes the HIF-2α (hypoxia-inducible factor-2α) in the cytotrophoblasts. HIF-2α signaling impairs trophoblast differentiation and increases sFLT-1 (soluble fms-like tyrosine kinase-1) secretion, which reduces fetal growth and causes maternal symptoms. This study aims to evaluate the benefits of using PT2385—an oral specific HIF-2α inhibitor—to treat severe placental dysfunction. Methods: To evaluate its therapeutic potential, PT2385 was first studied in primary human cytotrophoblasts isolated from term placenta and exposed to 2.5% O 2 to stabilize HIF-2α. Viability and luciferase assays, RNA sequencing, and immunostaining were used to analyze differentiation and angiogenic factor balance. The ability of PT2385 to mitigate maternal manifestations of preeclampsia was studied in the selective reduced uterine perfusion pressure model performed in Sprague-Dawley rats. Results: In vitro, RNA sequencing analysis and conventional techniques showed that treated cytotrophoblast displayed an enhanced differentiation into syncytiotrophoblasts and normalized angiogenic factor secretion compared with vehicle-treated cells. In the selective reduced uterine perfusion pressure model, PT2385 efficiently decreased sFLT-1 production, thus preventing the onset of hypertension and proteinuria in pregnant dams. Conclusions: These results highlight HIF-2α as a new player in our understanding of placental dysfunction and support the use of PT2385 to treat severe preeclampsia in humans.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Internal Medicine

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