Opendata, web and dolomites

ACE-OF-SPACE SIGNED

Analysis, control, and engineering of spatiotemporal pattern formation

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 ACE-OF-SPACE project word cloud

Explore the words cloud of the ACE-OF-SPACE project. It provides you a very rough idea of what is the project "ACE-OF-SPACE" about.

orchestrate    zebrafish    developmental    space    central    form    engineering    differentiate    mysterious    bmp    regulated    break    mathematical    extra    previously    indicates    axis    population    unknown    insights    patterning    adult    suggest    pattern    identical    organize    signals    embryos    optogenetics    begun    diffusion    vertebrate    allocation    mouse    analyze    thought    self    systems    plan    beta    superfamily    mammalian    experimentally    mechanism    reaction    bacterial    molecules    signaling    opens    cells    interact    opposing    tissues    symmetry    theoretical    prior    underlying    biology    organizing    biophysical    sufficient    independent    temporally    quantitative    initially    absence    body    members    combination    demonstrated    arise    asymmetric    colonies    mediated    axes    understand    minimal    maternal    imaging    tissue    strategies    time    modeling    asymmetries    signal    unclear    cross    questions    patterned    talk    mechanisms    cell    risk    precursors    nodal    small    sources    tgf    secondary    organ    synthetic    stem    homogeneous    stability    first    embryonic    embryogenesis    engineer    patterns    gain   

Project "ACE-OF-SPACE" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: MUENCHEN
postcode: 80539
website: n.a.

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 Germany [DE]
 Total cost 1˙997˙750 €
 EC max contribution 1˙997˙750 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-COG
 Funding Scheme ERC-COG
 Starting year 2020
 Duration (year-month-day) from 2020-07-01   to  2025-06-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) coordinator 1˙997˙750.00

Map

 Project objective

A central problem in developmental biology is to understand how tissues are patterned in time and space - how do identical cells differentiate to form the adult body plan? Patterns often arise from prior asymmetries in developing embryos, but there is also increasing evidence for self-organizing mechanisms that can break the symmetry of an initially homogeneous cell population. These patterning processes are mediated by a small number of signaling molecules, including the TGF-β superfamily members BMP and Nodal. While we have begun to analyze how biophysical properties such as signal diffusion and stability contribute to axis formation and tissue allocation during vertebrate embryogenesis, three key questions remain. First, how does signaling cross-talk control robust patterning in developing tissues? Opposing sources of Nodal and BMP are sufficient to produce secondary zebrafish axes, but it is unclear how the signals interact to orchestrate this mysterious process. Second, how do signaling systems self-organize to pattern tissues in the absence of prior asymmetries? Recent evidence indicates that axis formation in mammalian embryos is independent of maternal and extra-embryonic tissues, but the mechanism underlying this self-organized patterning is unknown. Third, what are the minimal requirements to engineer synthetic self-organizing systems? Our theoretical analyses suggest that self-organizing reaction-diffusion systems are more common and robust than previously thought, but this has so far not been experimentally demonstrated. We will address these questions in zebrafish embryos, mouse embryonic stem cells, and bacterial colonies using a combination of quantitative imaging, optogenetics, mathematical modeling, and synthetic biology. In addition to providing insights into signaling and development, this high-risk/high-gain approach opens exciting new strategies for tissue engineering by providing asymmetric or temporally regulated signaling in organ precursors.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "ACE-OF-SPACE" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

The information about "ACE-OF-SPACE" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

evolSingleCellGRN (2019)

Constraint, Adaptation, and Heterogeneity: Genomic and single-cell approaches to understanding the evolution of developmental gene regulatory networks

Read More  

IMMUNOTHROMBOSIS (2019)

Cross-talk between platelets and immunity - implications for host homeostasis and defense

Read More  

RODRESET (2019)

Development of novel optogenetic approaches for improving vision in macular degeneration

Read More