Vascular Endothelial Growth Factor Receptor 2 (VEGFR-2) Functions to Promote Uterine Decidual Angiogenesis during Early Pregnancy in the Mouse

• Published in: Endocrinology (Philadelphia) Vol. 150; no. 8; pp. 3845 - 3854
• Main Authors: Douglas, Nataki C, Tang, Hongyan, Gomez, Raul, Pytowski, Bronislaw, Hicklin, Daniel J, Sauer, Christopher M, Kitajewski, Jan, Sauer, Mark V, Zimmermann, Ralf C
• Format: Journal Article
• Language: English
• Published: Chevy Chase, MD Endocrine Society 01.08.2009; The Endocrine Society
• Subjects: Animals; Antibodies, Monoclonal - pharmacology; Apoptosis; Biological and medical sciences; Cell Proliferation; Decidua - blood supply; Decidua - drug effects; Decidua - metabolism; Embryonic Development - drug effects; Embryonic Development - physiology; Female; Fluorescent Antibody Technique; Fundamental and applied biological sciences. Psychology; Immunohistochemistry; Male; Mice; Neovascularization, Physiologic - drug effects; Neovascularization, Physiologic - physiology; Ovariectomy; Pregnancy; Reverse Transcriptase Polymerase Chain Reaction; Uterus - drug effects; Uterus - metabolism; Vascular Endothelial Growth Factor Receptor-1 - antagonists & inhibitors; Vascular Endothelial Growth Factor Receptor-1 - metabolism; Vascular Endothelial Growth Factor Receptor-1 - physiology; Vascular Endothelial Growth Factor Receptor-2 - antagonists & inhibitors; Vascular Endothelial Growth Factor Receptor-2 - metabolism; Vascular Endothelial Growth Factor Receptor-2 - physiology; Vascular Endothelial Growth Factor Receptor-3 - antagonists & inhibitors; Vascular Endothelial Growth Factor Receptor-3 - metabolism; Vascular Endothelial Growth Factor Receptor-3 - physiology; Vertebrates: endocrinology; Angiogenesis; Vertebrata; Mammalia; Vascular endothelium growth factor; Mouse; Uterus; Animal; Female genital system; Rodentia; Early pregnancy; Biological receptor
• ISSN: 0013-7227; 1945-7170
• DOI: 10.1210/en.2008-1207

Implantation of an embryo induces rapid proliferation and differentiation of uterine stromal cells, forming a new structure, the decidua. One salient feature of decidua formation is a marked increase in maternal angiogenesis. Vascular endothelial growth factor (VEGF)-dependent pathways are active in the ovary, uterus, and embryo, and inactivation of VEGF function in any of these structures might prevent normal pregnancy development. We hypothesized that decidual angiogenesis is regulated by VEGF acting through specific VEGF receptors (VEGFRs). To test this hypothesis, we developed a murine pregnancy model in which systemic administration of a receptor-blocking antibody would act specifically on uterine angiogenesis and not on ovarian or embryonic angiogenesis. In our model, ovarian function was replaced with exogenous progesterone, and blocking antibodies were administered prior to embryonic expression of VEGFRs. After administration of a single dose of the anti-VEGFR-2 antibody during the peri-implantation period, no embryos were detected on embryonic d 10.5. The pregnancy was disrupted because of a significant reduction in decidual angiogenesis, which under physiological conditions peaks on embryonic d 5.5 and 6.5. Inactivation of VEGFR-3 reduced angiogenesis in the primary decidual zone, whereas administration of VEGFR-1 blocking antibodies had no effect. Pregnancy was not disrupted after administration of anti-VEGFR-3 or anti-VEGFR-1 antibodies. Thus, the VEGF/VEGFR-2 pathway plays a key role in the maintenance of early pregnancy through its regulation of peri-implantation angiogenesis in the uterine decidua. This newly formed decidual vasculature serves as the first exchange apparatus for the developing embryo until the placenta becomes functionally active. The VEGF/VEGFR-2 pathway plays a key role in maintaining early pregnancy in the mouse through its regulation of peri-implantation angiogenesis in the uterine decidua.