Objective
Adult zebrafish are capable of completely regenerating their heart after an extensive insult. Previously, we determined that the regenerated myocardium was produced by the proliferation of existing cardiomyocytes and not, as had previously been reported, by stem/progenitor cells. Analysis of regenerating hearts shows that soon after injury cardiomyocytes detach from one another and dedifferentiate, disassembling their sarcomeric structure in the process. In situ and microarray analysis indicate that dynamic changes in gene expression are also associated with heart regeneration. At present only handful of genes have been directly linked to heart regeneration in zebrafish. Our main objective is to expand this small list and thus provide candidates which can subsequently be manipulated in mammals. To determine suitable target genes, we will make use of the substantial microarray data generated from studying heart regeneration in zebrafish. Importantly, this data has revealed that certain genes shown to be up-regulated during zebrafish heart regeneration have previously been shown to positively regulate cardiomyocyte proliferation in mammalian models. These findings not only indicate that zebrafish and mammals share similar genetic mechanisms as far as regulating cardiomyocyte proliferation but also verify that the data represented in the microarrays contains positive candidate genes. Once candidates have been selected and confirmed in our zebrafish model system, we will begin testing these in vitro in mammalian cardiomyocytes before creating transgenic mouse models to determine whether they are capable of inducing myocardial regeneration following cardiac ischemia.
Fields of science (EuroSciVoc)
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
CORDIS classifies projects with EuroSciVoc, a multilingual taxonomy of fields of science, through a semi-automatic process based on NLP techniques. See: The European Science Vocabulary.
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Programme(s)
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Multi-annual funding programmes that define the EU’s priorities for research and innovation.
Topic(s)
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Calls for proposals are divided into topics. A topic defines a specific subject or area for which applicants can submit proposals. The description of a topic comprises its specific scope and the expected impact of the funded project.
Call for proposal
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
Procedure for inviting applicants to submit project proposals, with the aim of receiving EU funding.
FP7-PEOPLE-2012-CIG
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Funding Scheme
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
Funding scheme (or “Type of Action”) inside a programme with common features. It specifies: the scope of what is funded; the reimbursement rate; specific evaluation criteria to qualify for funding; and the use of simplified forms of costs like lump sums.
MC-CIG - Support for training and career development of researcher (CIG)
Coordinator
75794 Paris
France
The total costs incurred by this organisation to participate in the project, including direct and indirect costs. This amount is a subset of the overall project budget.