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HumanPlacenta SIGNED

Human Placental Development and the Uterine Microenvironment

Total Cost €

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EC-Contrib. €

0

Partnership

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 HumanPlacenta project word cloud

Explore the words cloud of the HumanPlacenta project. It provides you a very rough idea of what is the project "HumanPlacenta" about.

trophoblast    dangerous    crispr    ranging    invasion    fetal    organ    depends    editing    culture    human    physiology    scaffolds    trophectoderm    infiltrate    seeded    territorial    cas9    faithfully    genome    organoids    stromal    placental    single    molecular    influenced    lineage    immune    remarkable    models    stillbirth    glands    evt    tools    interactions    placentation    arteries    decidua    spiral    regulating    cell    cells    stages    eclampsia    remodelling    wall    mechanisms    invade    artificial    extravillous    balance    tissue    vessel    embryonic    extra    lack    reproductive    decidual    capitalises    made    boundary    earliest    practical    central    potentially    normal    fetus    model    maternal    genomics    how    mucosa    conductance    transform    pregnancy    organoid    limitations    drawn    paracrine    cultures    engineering    signalling    glandular    restriction    collagen    environment    successful    excessive    specify    3d    ethical    vitro    microenvironment    deficient    uterine    questions    cellular    arterial    combined    dilated    placenta    miscarriage    underlying   

Project "HumanPlacenta" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.ac.uk

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country United Kingdom [UK]
 Total cost 1˙992˙098 €
 EC max contribution 1˙992˙098 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-STG
 Funding Scheme ERC-STG
 Starting year 2020
 Duration (year-month-day) from 2020-03-01   to  2025-02-28

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 1˙992˙098.00

Map

Leaflet | Map data © OpenStreetMap contributors, CC-BY-SA, Imagery © Mapbox

 Project objective

How does the human placenta develop and how is this influenced by the maternal uterine microenvironment? These are the central questions addressed in my proposal. Normal growth and development of the fetus depends on the placenta, the extra-embryonic organ derived from trophectoderm. Successful pregnancy depends on the earliest stages of development when placental extravillous trophoblast cells (EVT) infiltrate the uterine mucosa, the decidua. EVT invade the decidua to transform the uterine spiral arteries into a dilated vessel capable of high conductance. Deficient arterial remodelling by EVT results in miscarriage, pre-eclampsia, fetal growth restriction and stillbirth. However, excessive invasion into the uterine wall is also potentially dangerous. Thus, to achieve a successful pregnancy, a territorial boundary is drawn with a balance between fetal EVT invasion and maternal decidual cells. Understanding the molecular and cellular mechanisms underlying these maternal/fetal interactions has been challenging due both to practical and ethical limitations and lack of reliable in vitro models. I have recently derived 3D culture systems (organoids) from human decidua and placenta that will provide the essential tools. I will use these organoids combined with single cell genomics, Crispr/Cas9 genome editing and tissue engineering to study: (i) the molecular mechanisms that specify the EVT lineage (ii) the role of paracrine signalling from maternal decidual glands in regulating placental development (iii) cell-cell interactions between decidua and EVT by creating an artificial model of decidua made from tailored collagen scaffolds seeded with stromal, glandular and immune cells. My proposal capitalises on the remarkable ability of organoid cultures to faithfully model human physiology. The human uterine environment in early pregnancy is crucial for reproductive success and development of an in vitro model of placentation will have a wide-ranging impact.

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The information about "HUMANPLACENTA" are provided by the European Opendata Portal: CORDIS opendata.

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