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NanoMechShape SIGNED

Molecular control of actin network architecture and mechanics during cell shape changes

Total Cost €

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EC-Contrib. €

0

Partnership

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 NanoMechShape project word cloud

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

regulation    first    molecular    elusive    super    pathologies    explore    biology    interdisciplinary    underlying    crosstalk    nanomechshape    exemplar    spreading    difficulty    rounded    cytokinetic    gap    architectural    regulatory    architecture    tension    furrow    physiology    organisation    driving    truly    regulated    animal    systematically    contractions    actin    compare    understand    comprise    membrane    network    investigations    networks    differentiation    thin    multidisciplinary    paving    categories    deformations    ing    cortex    cortical    primary    cell    morphogenesis    stem    unveil    microscopy    deregulation    establishment    principles    mouse    contractile    mechanisms    embryonic    heart    filopodia    fundamental    mitosis    shape    electron    resolution    fall    determinants    probing    gradient    fate    integrating    ingression    behaviors    precise    physics    bridging    morphology    nanoscale    cells    forces    transitions    lamellipodia   

Project "NanoMechShape" 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˙943˙071 €
 EC max contribution 1˙943˙071 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2018-COG
 Funding Scheme ERC-COG
 Starting year 2019
 Duration (year-month-day) from 2019-05-01   to  2024-04-30

 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˙943˙071.00

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 Project objective

Precise control of shape is key to cell physiology, and cell shape deregulation is at the heart of many pathologies. As cell morphology is controlled by forces, studies integrating physics with biology are required to truly understand morphogenesis. NanoMechShape will take such an interdisciplinary approach to investigate the regulation of animal cell shape. In animal cells, actin networks are the primary determinants of shape. Most cell shape changes fall into two categories: 1) those driven by contractions of the actin cortex, a thin network underlying the membrane in rounded cells; and 2) those resulting from transitions between the cortex and other actin networks, such as lamellipodia and filopodia. To understand cell deformations, it is thus essential to understand the regulation of cortex contractile tension and the mechanisms controlling transitions in actin architecture. NanoMechShape will comprise three aims. First, we will explore how cortex tension is regulated. We will focus on the role of cortex architecture, which remains elusive due to the difficulty in probing the organisation of the thin cortical network. We will unveil cortex architecture using super-resolution and electron microscopy, and systematically investigate how nanoscale architectural features affect tension. Second, we will explore how the identified regulatory mechanisms contribute to the establishment of a cortical tension gradient. We will focus on the gradient driving cytokinetic furrow ingression, an exemplar tension-driven shape change. Third, we will investigate transitions in actin architecture underlying cell spreading. We will compare spreading at the end of mitosis and during differentiation of mouse embryonic stem cells, paving the way to investigations of the crosstalk between cell shape and fate. By bridging a fundamental gap between molecular processes and cell-scale behaviors, our multidisciplinary study will unveil some of the fundamental principles of cell morphogenesis.

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

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