NSCaging | Behavior and molecular signature of Neural Stem Cells, and changes occurring during aging

Summary
In the adult neurogenic niches, neural stem cells (NSCs) generate neurons throughout life. During aging, the number of newborn neurons is clearly reduced, although it is still very debated what specifically happens to the NSCs: do they die, increase their quiescence or change their fate? It is emerging that NSCs are heterogeneous, with different subtypes, in particular quiescent and active NSCs, responding differently to neurogenic stimuli, including aging. However, due to difficulties in distinguishing NSCs subtypes in vivo, their behavior in the physiological environment, their molecular hallmarks, and especially how those are changed during aging are still elusive. These are key questions in neuroscience and stem cell biology. Thanks to the combination of the host laboratory expertise with mine, the current action proposes to develop a strategy to discriminate different NSCs in vivo and shed new light on their behavior, molecular properties and the changes occurring during life. The expected results are going to provide critical information on the regenerative potential of NSCs subtypes and on whether and how the aging phenotype can be reverted, with a consequent strong scientific and social impact.
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More information & hyperlinks
Web resources: https://cordis.europa.eu/project/id/656601
Start date: 01-04-2016
End date: 31-03-2018
Total budget - Public funding: 165 598,80 Euro - 165 598,00 Euro
Cordis data

Original description

In the adult neurogenic niches, neural stem cells (NSCs) generate neurons throughout life. During aging, the number of newborn neurons is clearly reduced, although it is still very debated what specifically happens to the NSCs: do they die, increase their quiescence or change their fate? It is emerging that NSCs are heterogeneous, with different subtypes, in particular quiescent and active NSCs, responding differently to neurogenic stimuli, including aging. However, due to difficulties in distinguishing NSCs subtypes in vivo, their behavior in the physiological environment, their molecular hallmarks, and especially how those are changed during aging are still elusive. These are key questions in neuroscience and stem cell biology. Thanks to the combination of the host laboratory expertise with mine, the current action proposes to develop a strategy to discriminate different NSCs in vivo and shed new light on their behavior, molecular properties and the changes occurring during life. The expected results are going to provide critical information on the regenerative potential of NSCs subtypes and on whether and how the aging phenotype can be reverted, with a consequent strong scientific and social impact.

Status

CLOSED

Call topic

MSCA-IF-2014-EF

Update Date

28-04-2024
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Horizon 2020
H2020-EU.1. EXCELLENT SCIENCE
H2020-EU.1.3. EXCELLENT SCIENCE - Marie Skłodowska-Curie Actions (MSCA)
H2020-EU.1.3.2. Nurturing excellence by means of cross-border and cross-sector mobility
H2020-MSCA-IF-2014
MSCA-IF-2014-EF Marie Skłodowska-Curie Individual Fellowships (IF-EF)