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OPTOLEADER SIGNED

Optogenetic control of leader cell mechanobiology during collective cell migration

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 OPTOLEADER project word cloud

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

morphogenesis    create    array    expressing    epithelial    reversible    modifications    performed    perform    transduced    integral    blue    wound    prominently    leaders    invasion    express    mechanical    confluent    waves    substrates    optogenetics    monolayers    tools    extracellular    behaviours    proteins    exhibiting    sensitive    play    situations    confined    dimensional    traction    phenomena    collective    arising    intracellular    migrating    fundamental    cancer    guide    monolayer    force    physiologically    stress    emergent    directional    flocks    hallmark    healing    adhesion    quantification    microscopy    physical    ecm    cells    vivo    transduction    shed    latter    paving    groups    largely    multicellular    experimental    functionalized    active    actions    motility    modulate    contribution    biology    light    forces    cohesive    molecular    physically    leader    biological    influence    migratory    physics    activators    flocking    cell    orchestrated    rhogtpases    matrix    combines    migration    generate   

Project "OPTOLEADER" data sheet

The following table provides information about the project.

Coordinator
FUNDACIO INSTITUT DE BIOENGINYERIA DE CATALUNYA 

Organization address
address: CARRER BALDIRI REIXAC PLANTA 2A 10-12
city: BARCELONA
postcode: 8028
website: http://www.ibecbarcelona.eu

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 Spain [ES]
 Total cost 158˙121 €
 EC max contribution 158˙121 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-09-01   to  2021-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FUNDACIO INSTITUT DE BIOENGINYERIA DE CATALUNYA ES (BARCELONA) coordinator 158˙121.00

Map

 Project objective

Emergent collective behaviours such as flocks and waves are a hallmark of biological active matter, and occur prominently also in large groups of migrating epithelial cells, where they are involved in fundamental biological processes such as wound healing, morphogenesis and cancer cell invasion. Physical forces transduced between cells and arising between cells and the extracellular matrix (ECM) play an integral role in orchestrated multicellular phenomena. Another integral contribution is given by the actions of leader cells, that modulate and guide the migration of cohesive cell groups. How leader cells achieve this using intracellular and cell-ECM forces remains largely to be understood. Here we propose an experimental approach to generate leader cells using optogenetics and to study how leaders influence the collective behaviour of migratory cell groups. We will use epithelial cells expressing light-sensitive activators of RhoGTPases, which enable reversible and directional control of cell motility using blue light. Traction force microscopy and monolayer stress microscopy will be performed using these cells while we will create and control leaders. With functionalized substrates, we will study the mechanical role of leaders in different conditions, from confined two-cell systems to confluent monolayers exhibiting flocking. Finally, we will express the light-sensitive proteins in cancer cells, to study how their three-dimensional dissemination is affected by leaders. Our experimental approach combines physics-derived modelling and quantification of forces with advanced molecular biology tools. The latter will enable us to perform selected modifications on cells, targeting a wide array of proteins involved in cell-cell adhesion and force transduction. Our goal is to shed light on how leaders physically influence collective migration in physiologically relevant situations, paving the way for the in vivo applications of light-induced leader cells.

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