Retinoic acid regulates fetoplacental vascularization via notch signaling and a SEMA3E/F-PLEXIND1 axis
Aleksandra Cwiek, Umadevi Paila, Zaneta Markowska, Nafiisha Genet, Madeline Jackson, Gael Genet, Shelby R. Cain, Jordon W. Aragon, Elizabeth A. Nelson, Ricardo Moraes Borges, Ann E. Sutherland, Karen K. Hirschi

TL;DR
Retinoic acid helps form proper blood vessels in the placenta by controlling cell growth and signaling pathways.
Contribution
This study identifies a new mechanism by which retinoic acid regulates placental vascularization through Notch and SEMA3E/F-PLEXIND1 signaling.
Findings
RA deficiency causes placental endothelial hyperproliferation and impaired vascular remodeling.
RA regulates endothelial growth and vascular remodeling via Notch signaling.
RA controls endothelial guidance through a SEMA3E/F-PLEXIND1 signaling axis.
Abstract
The placenta is vital for fetal development, and altered placental vascularization, the most common placental pathology, underlies prevalent disorders, including fetal growth restriction, prematurity, and pregnancy complications. Impaired placental vascularization is associated with Vitamin A deficiency, but the mechanisms are undefined. To investigate this, we used retinoic acid (RA)-deficient Raldh2−/− embryos, and found they exhibit allantoic and placental endothelial hyperproliferation and impaired arterial-venous remodeling, which were rescued by providing all-trans-RA (ATRA) via maternal diet. Single-cell RNA sequencing of E9.5 Raldh2+/+, Raldh2−/−, and Raldh2−/− + ATRA placental cells, and functional assays, revealed that RA regulates endothelial growth and vascular remodeling via Notch signaling. We also uncovered a PLEXIND1–SEMA3E/F signaling axis between fetal endothelial…
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Taxonomy
TopicsRetinoids in leukemia and cellular processes · Pregnancy and preeclampsia studies · Protease and Inhibitor Mechanisms
