Artículo

Vasoactive intestinal peptide shapes first-trimester placenta trophoblast, vascular, and immune cell cooperation

Paparini, Daniel Esteban Icon; Choudhury, Ruhul H. ; Vota, Daiana Marina Icon; Karolczak Bayatti, Magdalena ; Finn Sell, Sarah ; Grasso, Esteban Nicolas Icon; Hauk, Vanesa Cintia Icon; Ramhorst, Rosanna Elizabeth Icon; Perez Leiros, Claudia Icon; Aplin, John D.

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Fecha

04/2019

Editorial

Wiley Blackwell Publishing, Inc

Revista

British Journal of Pharmacology

Título del libro

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Institución organizadora

ISSN

0007-1188

eISSN

ISBN

Idioma

Inglés

Tipo del evento

Clasificación temática

Resumen

Background and Purpose: Extravillous trophoblast (EVT) cells are responsible for decidual stromal invasion, vascular transformation, and the recruitment and functional modulation of maternal leukocytes in the first-trimester pregnant uterus. An early disruption of EVT function leads to placental insufficiency underlying pregnancy complications such as preeclampsia and fetal growth restriction. Vasoactive intestinal peptide (VIP) is a vasodilating and immune modulatory factor synthesized by trophoblast cells. However, its role in first-trimester placenta has not been explored. Here, we tested the hypothesis that VIP is involved in first-trimester EVT outgrowth, spiral artery remodelling, balancing angiogenesis, and maintenance of immune homeostasis. Experimental Approach: First-trimester placental tissue (five to nine weeks of gestation) was collected, and was used for EVT outgrowth experiments, immunofluorescence, isolation of decidual natural killer (dNK) cells and decidual macrophages (dMA), and functional assays. Peripheral blood monocytes were differentiated with GM-CSF and used for angiogenesis assays. Key Results: In decidua basalis, VIP+ EVT were observed sprouting from cell columns and lining spiral arterioles. EVT migrating from placental explants were also VIP+. VIP increased EVT outgrowth and IL-10 release, whereas it decreased pro-inflammatory cytokine production in EVT, dNK cells, and dMA. VIP disrupted endothelial cell networks, both directly and indirectly via an effect on macrophages. Conclusion and Implications: The results suggest that VIP assists the progress of EVT invasion and vessel remodelling in first-trimester placental bed in an immunologically “silent” milieu. The effects of VIP in the present ex vivo human placental model endorse its potential as a therapeutic candidate for deep placentation disorders.

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