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COMpetence of neural progenitors In Time

Project description

Neural progenitor competence for new therapies

During brain development, neural progenitor cells generate a diverse array of neuronal subtypes in precise numbers and proportions. However, the flexibility of this process across different progenitor populations and developmental stages remains poorly understood. Supported by the Marie Skłodowska-Curie Actions programme, the COMIT project will study neural progenitor competence in the zebrafish hindbrain using the TEMPO2.0 lineage tracing system. It will track progenitor populations during differentiation, analysing their contributions to glutamatergic and GABAergic neurons. The project will also assess the role of specific transcription factors in neuronal subtype specification and identify their genomic targets. These findings could inform new cell therapy strategies for neurodevelopmental and neurodegenerative diseases.

Objective

During brain development, neural progenitor cells generate an enormous diversity of neuronal subtypes in the correct numbers and proportions. Although the transition from progenitor cells to mature neurons is well studied, little is known about how plastic this process is among different progenitor populations and over time.

COMIT aims to investigate the temporal dynamics of neural progenitor competence. Using the zebrafish embryonic brainstem the hindbrain as a model system and an innovative multicolour lineage tracing system TEMPO2.0 I will label and track different generations of specific neural progenitor populations as they progress through differentiation. Leveraging multiple transgenic zebrafish lines, I will monitor the contribution of these progenitors to glutamatergic and GABAergic neuron populations across different temporal windows. Further, I will challenge progenitor competence through heterochronical expression of temporal identity transcription factors, assessing their impact on neuronal subtype specification. Chromatin profiling will be employed to identify the genomic targets of re-specification factors, shedding light on the molecular mechanisms that regulate progenitor plasticity.

This integrated approach, combining cutting-edge biocomputing, imaging, genetic, and molecular techniques, will provide key insights into the heterogeneity of neural progenitor competence and the mechanisms that control the generation of neuronal diversity. Ultimately, the findings from this research could pave the way for new cell therapy strategies targeting neurodevelopmental and neurodegenerative diseases.

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Topic(s)

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HORIZON-TMA-MSCA-PF-EF - HORIZON TMA MSCA Postdoctoral Fellowships - European Fellowships

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Call for proposal

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(opens in new window) HORIZON-MSCA-2024-PF-01

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Coordinator

UNIVERSIDAD POMPEU FABRA
Net EU contribution

Net EU financial contribution. The sum of money that the participant receives, deducted by the EU contribution to its linked third party. It considers the distribution of the EU financial contribution between direct beneficiaries of the project and other types of participants, like third-party participants.

€ 194 074,56
Address
PLACA DE LA MERCE, 10-12
08002 Barcelona
Spain

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Region
Este Cataluña Barcelona
Activity type
Higher or Secondary Education Establishments
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Total cost

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