Opendata, web and dolomites

StemCellHabitat SIGNED

Metabolic and Timed Control of Stem Cell Fate in the Developing Animal

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 StemCellHabitat project word cloud

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

provides    mechanisms    melanogaster    dissect    progeny    proliferation    imaging    eukaryotes    fate    cycle    organism    first    levels    animal    cell    nbs    transcription    right    question    waves    integrating    dynamics    disappear    live    generation    formed    phosphorylation    decisions    evident    additional    regulator    oxidative    genetics    developmental    metabolite    omics    unclear    positions    stage    previously    cues    dynamically    scs    correct    brain    directing    time    contributes    cells    fantastic    lineage    metabolism    regulation    found    complexity    physiological    regulated    metabolically    stem    combining    little    tight    mechanistic    proper    age    regulates    exit    drosophila    details    temporally    sc    neurons    spatial    integrative    nb    hormones    combination    stereotypical    model    multidisciplinary    regulate    tumors    answer    neural    metabolic    sorting    highlighting    occurs    unlimited    types    neuroblasts    temporal    fixed    3d   

Project "StemCellHabitat" data sheet

The following table provides information about the project.

Coordinator
UNIVERSIDADE NOVA DE LISBOA 

Organization address
address: CAMPUS DE CAMPOLIDE
city: LISBOA
postcode: 1099 085
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 Portugal [PT]
 Total cost 1˙697˙493 €
 EC max contribution 1˙697˙493 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-02-01   to  2023-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSIDADE NOVA DE LISBOA PT (LISBOA) coordinator 1˙017˙858.00
2    INSTITUTO DE BIOLOGIA EXPERIMENTAL E TECNOLOGICA PT (OEIRAS) participant 679˙635.00

Map

 Project objective

Stem cell (SC) proliferation during development requires tight spatial and temporal regulation to ensure correct cell number and right cell types are formed at the proper positions. Currently very little is known about how SCs are regulated during development. Specifically, it is unclear how SC waves of proliferation are regulated and how the fate of their progeny changes during development. In addition, it has recently become evident that metabolism provides additional complexity in cell fate regulation, highlighting the need for integrating metabolic information across physiological levels. This project will answer the question of how the combination of metabolic state and temporal cues (animal developmental stage) regulate SC fate. I will use Drosophila melanogaster, an animal complex enough to be similar to higher eukaryotes and yet simple enough to dissect the mechanistic details of cell regulation and its impact on the organism. Drosophila neural stem cells, the neuroblasts (NB), are a fantastic model of temporally and metabolically regulated cells. NB lineage fate changes with time, directing the generation of a stereotypical set of neurons, after which they disappear. I have previously found that metabolism is an important regulator of NB cell cycle exit, which occurs in response to an increase in levels of oxidative phosphorylation. Using a multidisciplinary approach combining genetics, cell type/age sorting, multi-omics analysis, fixed and 3D-live NB imaging and metabolite dynamics, I propose an integrative approach to investigate how NBs are regulated in the developing animal. First I will dissect the mechanisms by which metabolism regulates NB fate. Second, I will investigate how metabolism contributes to NB unlimited proliferation and brain tumors. Finally, we will address how temporal transcription factors and hormones dynamically affect cell fate decisions during development.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "STEMCELLHABITAT" 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 "STEMCELLHABITAT" are provided by the European Opendata Portal: CORDIS opendata.

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

CohoSing (2019)

Cohomology and Singularities

Read More  

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More  

CUSTOMER (2019)

Customizable Embedded Real-Time Systems: Challenges and Key Techniques

Read More