Abstract

With implantation, mouse stromal cells begin to transform into epithelial-like cells surrounding the implantation chamber forming an avascular zone called the primary decidual zone (PDZ). In the mouse, the PDZ forms a transient, size-dependent permeable barrier to protect the embryo from maternal circulating harmful agents. The process of decidualization is critical for pregnancy maintenance in mice and humans. Mice deficient in cannabinoid receptors, CB1 and CB2, show compromised PDZ with dysregulated angiogenic factors, resulting in the retention of blood vessels and macrophages. This phenotype is replicated in Cnr1-/- but not in Cnr2-/-mice. In vitro decidualization models suggest that Cnr1 levels substantially increase in mouse and human decidualizing stromal cells, and that neutralization of CB1 signaling suppresses decidualization and misregulates angiogenic factors. Taken together, we propose that implantation quality depends on appropriate angiogenic events driven by the integration of CB2 in endothelial cells and CB1 in decidual cells.

Highlights

  • Decidualization is a critical pregnancy event that follows embryo implantation

  • We investigated the roles of endocannabinoid signaling in decidualization using mouse models with suppressed CB1 and CB2 and a primary culture of Cnr1-/- stromal cells

  • We showed that Cnr1-/-Cnr2-/- uteri have defective decidualization and consequent increases in midgestational resorption rates

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Summary

Introduction

Decidualization is a critical pregnancy event that follows embryo implantation. During the initial stages of decidualization in mice, stromal cells transform into epithelioid cells (epithelial-like) surrounding the implanting embryo and form an avascular zone. This region is called the primary decidual zone (PDZ) and is critical to embryo development and successful pregnancy outcomes in mice (1). Because the PDZ is avascular, this zone is devoid of maternal immune cells, which protects embryos from circulating maternal insults (2). We have shown that Scribble (Scrib), a scaffold protein and a component of the planar cell polarity (PCP), plays a key role in PDZ formation (3). Molecular regulation in the formation of the PDZ is still far from clear

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