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StemCellHabitat SIGNED

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

Total Cost €

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EC-Contrib. €

0

Partnership

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 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.

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

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.

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

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