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Expansion microscopy in zebrafish embryo to study primary cilia function during...

Expansion microscopy in zebrafish embryo to study primary cilia function during cardiovascular development and diseases This project aims at revealing the function of primary cilia during cardiovascular development and cardiovascular diseases, with a specific focus on cardiac valves, through an imaging approach based on expansion light microscopy.... ver más

31/05/2023

IMPERIAL COLLEGE O...

213K€

Presupuesto del proyecto: 213K€

Líder del proyecto

IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND ME... No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Fecha límite participación Sin fecha límite de participación.

Financiación concedida El organismo H2020 notifico la concesión del proyecto el día 2023-05-31

MSCA-IF-2020: Individual Fellowships

I+D

Cerrada hace 4 años

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No hay información privada compartida para este proyecto. Habla con el coordinador.

1 Participantes

IMPERIAL COLLEGE OF SCIENCE...

212.93K€ | Lider

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Duración del proyecto: 26 meses Fecha Inicio: 2021-03-24
Fecha Fin: 2023-05-31

Líder del proyecto

IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND ME... No se ha especificado una descripción o un objeto social para esta compañía.

TRL 4-5

Presupuesto del proyecto 213K€

Fecha límite de participación Sin fecha límite de participación.

Descripción del proyecto This project aims at revealing the function of primary cilia during cardiovascular development and cardiovascular diseases, with a specific focus on cardiac valves, through an imaging approach based on expansion light microscopy. Cilia are evolutionary conserved organelles, involved in fundamental processes such as motility, signalling and mechano-sensing, associated with a group of developmental diseases termed ciliopathies. Cardiovascular defects are common in patients diagnosed with ciliopathies and genetic studies have identified mutations in genes coding for ciliary proteins in patient suffering from congenital heart diseases, suggesting an important role for this organelle in cardiogenesis. In particular, it has been shown that DZIP1, a cilia related protein involved in ciliogenesis, is mutated in patients. However, little is known about molecular mechanisms underlying DZIP1 abnormal function at developmental stages of valvulopathies. Using an innovative imaging-based approach in human ciliated cells and in zebrafish, we will investigate if cilia assembly, maintenance and disassembly are correlated with essential regulatory functions of DZIP1 during cardiogenesis, more precisely in endocardial cells (EdCs) during valvulogenesis. We will test if the protein DZIP1/Iguana function is not restricted to ciliogenesis in differentiated cells, but displays dynamic functions at centrioles and in the cytoplasm, that are important for tissue-remodelling. My multidisciplinary approach will allow me to tackle this question from the molecular and structural to the cellular and tissue-scale.

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