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EVALVE SIGNED

Biomechanics and signaling in models of congenital heart valve defects

Total Cost €

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EC-Contrib. €

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Partnership

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 EVALVE project word cloud

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

cardiac    optical    3d    resolution    combined    mrna    form    physiology    loops    biomechanical    integrate    critical    modulate    unraveling    mechanical    lineage    directed    fundamental    valves    abnormal    live    mathematical    edcs    diseases    amongst    subcellular    structures    extracellular    challenged    programs    fetal    links    beats    molecular    quiescent    microscopy    either    pathological    body    normally    made    morphogenesis    embryogenesis    interactions    lab    lifetime    forces    function    origins    light    pioneered    mediated    human    functional    mechanically    sequencing    defects    cell    interventions    congenital    shed    stress    adulthood    biological    reporters    mechanosensitivity    hemodynamic    times    cardiovascular    elucidation    heart    signs    billion    chip    mechanotransduction    expression    gene    quantify    aberrant    components    feedback    understand    modeling    organize    activated    endothelial    mechanism    matrix    cells    therapeutic    developmental    transcriptional    little    valve    network    throughput    mechanosensors    repair    explored    tweezing    re    endocardial    roles   

Project "EVALVE" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.ac.uk/

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
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 Coordinator Country United Kingdom [UK]
 Project website http://www.igbmc.fr/research/department/1/team/15/
 Total cost 2˙000˙000 €
 EC max contribution 2˙000˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2015-CoG
 Funding Scheme ERC-COG
 Starting year 2016
 Duration (year-month-day) from 2016-12-01   to  2021-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 798˙871.00
2    CENTRE EUROPEEN DE RECHERCHE EN BIOLOGIE ET MEDECINE FR (ILLKIRCH GRAFFENSTADEN) participant 1˙201˙128.00

Map

 Project objective

Mechanical forces are fundamental to cardiovascular development and physiology. The interactions between mechanical forces and endothelial cells are mediated by mechanotransduction feedback loops. My lab is interested in understanding how hemodynamic forces modulate cardiovascular function and morphogenesis. Overall, our recent work is unraveling the biological links between mechanical forces, mechanotransduction and endothelial cell responses. The heart beats 2.6 billion times in a human lifetime and heart valves are amongst the most mechanically challenged structures of the body. The cardiac valves are made of endocardial cells (EdCs) and extracellular matrix components. Most valve diseases have their origins in embryogenesis, either as signs of abnormal developmental processes or the aberrant re-expression of fetal gene programs normally quiescent in adulthood.

This project is directed towards the elucidation of the biomechanical mechanism of mechanotransduction at the subcellular and molecular level and in addressing how EdCs integrate this information to form and maintain a functional cardiac valve. We will identify the mechanosensors at work in EdCs and their roles during cardiac valve development and repair. To do so, we will implement unique optical methodologies the lab has pioneered to characterize endocardial mechanotransduction: 1) Optical tweezing combined with mechanical stress reporters to test the mechanosensitivity of EdCs; 2) High resolution live microscopy and mathematical modeling to quantify mechanical forces; 3) 3D cell lineage studies to understand how cells respond and organize during pathological valve development. We will also use high-throughput mRNA- and ChIP-sequencing to characterize the transcriptional network activated by forces.

When completed this proposal will shed light on a critical, but little explored, aspect of congenital valve defects and will be useful for identifying new targets for therapeutic interventions.

 Publications

year authors and title journal last update
List of publications.
2017 Renee Wei-Yan Chow, Julien Vermot
The rise of photoresponsive protein technologies applications in vivo: a spotlight on zebrafish developmental and cell biology
published pages: 459, ISSN: 2046-1402, DOI: 10.12688/f1000research.10617.1
F1000Research 6 2020-01-29
2017 Renee Wei-Yan Chow, Julien Vermot
The rise of photoresponsive protein technologies applications in vivo: a spotlight on zebrafish developmental and cell biology
published pages: 459, ISSN: 2046-1402, DOI: 10.12688/f1000research.10617.1
F1000Research 6 2020-01-29
2018 Renee Wei-Yan Chow, Paola Lamperti, Emily Steed, Francesco Boselli, Julien Vermot
Following Endocardial Tissue Movements via Cell Photoconversion in the Zebrafish Embryo
published pages: , ISSN: 1940-087X, DOI: 10.3791/57290
Journal of Visualized Experiments 132 2020-01-29
2017 Lauren M. Goddard, Anne-Laure Duchemin, Harini Ramalingan, Bingruo Wu, Mei Chen, Sharika Bamezai, Jisheng Yang, Li Li, Michael P. Morley, Tao Wang, Marielle Scherrer-Crosbie, David B. Frank, Kurt A. Engleka, Stephen C. Jameson, Edward E. Morrisey, Thomas J. Carroll, Bin Zhou, Julien Vermot, Mark L. Kahn
Hemodynamic Forces Sculpt Developing Heart Valves through a KLF2-WNT9B Paracrine Signaling Axis
published pages: 274-289.e5, ISSN: 1534-5807, DOI: 10.1016/j.devcel.2017.09.023
Developmental Cell 43/3 2020-01-29
2019 Rita R. Ferreira, Hajime Fukui, Renee Chow, Andrej Vilfan, Julien Vermot
The cilium as a force sensor−myth versus reality
published pages: jcs213496, ISSN: 0021-9533, DOI: 10.1242/jcs.213496
Journal of Cell Science 132/14 2020-01-29
2018 Rita R. Ferreira, Guillaume Pakula, Lhéanna Klaeyle, Hajime Fukui, Andrej Vilfan, Willy Supatto, Julien Vermot
Chiral Cilia Orientation in the Left-Right Organizer
published pages: 2008-2016.e4, ISSN: 2211-1247, DOI: 10.1016/j.celrep.2018.10.069
Cell Reports 25/8 2020-01-29
2018 Pedro Campinho, Paola Lamperti, Francesco Boselli, Julien Vermot
Three-dimensional microscopy and image analysis methodology for mapping and quantification of nuclear positions in tissues with approximate cylindrical geometry
published pages: 20170332, ISSN: 0962-8436, DOI: 10.1098/rstb.2017.0332
Philosophical Transactions of the Royal Society B: Biological Sciences 373/1759 2020-01-29

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