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The extracellular matrix as a mediator of cell-cell communication in cardiovascular inflammation

Project description

Insight into the role of the extracellular matrix in cardiovascular disease

The extracellular matrix (ECM) is a large network of proteins and other molecules that support and organise cells into tissues in the body. ECM is also emerging as a communication hub that transduces mechanical stimuli and facilitates cell-cell-interaction. Funded by the European Research Council, the MATRICARD project is interested in the role of ECM in cardiovascular disease. Researchers will therefore investigate the ECM composition during inflammatory conditions such as atherosclerosis and myocardial infarction and how it may influence disease progression. Project results will provide important knowledge on the mechanisms that regulate ECM in health and disease while the identification of therapeutic targets will help prevent cardiovascular disease.

Objective

Cardiovascular diseases, as coronary artery disease (CAD) and its sequelae myocardial infarction (MI) and heart failure, represent the leading cause of morbidity and mortality in industrialized and developing countries. Atherosclerosis is the pathology causing CAD and MI; both are characterized by a sterile inflammation with a chronic and acute course of the disease, respectively. There is a plethora of cell types, as leukocytes, endothelial cells, vascular smooth muscle cells, platelets, fibroblasts, and cardiomyocytes, which play important roles in the initiation, propagation, and termination of the pathophysiological processes. Recent data from genetic studies found that genetic variation influencing extracellular matrix (ECM) proteins is associated with cardiovascular diseases. We found that such proteins which are secreted by one cell type influence phenotypes of other cell types via, e.g. silencing of inflammatory functions or modulation of ECM composition. The ECM hence not only represents a meshwork in which cells are organized but also a communication hub to transduce mechanical stimuli and cell-cell-interaction signals. Here, we aim to explore the ECM proteome in sterile inflammatory diseases as atherosclerosis and MI in an unprecedented depth. We aim to identify novel regulators which give insights into the underlying processes and we will study the molecular and cellular mechanisms modifying the course of the disease. This will lead to the identification of novel therapeutic targets which might reshape our understanding of how these diseases occur and how we can prevent them, and to the development of novel, individualized treatment strategies. Finally, we aim to translate our findings to humans to get first insights on whether these strategies can be adapted and used in clinical trials. MATRICARD will go beyond technical boundaries and lead to a deep knowledge of ECM-mediated cell-cell-communication and reveal its translational potential.

Host institution

DEUTSCHES HERZZENTRUM MUNCHEN
Net EU contribution
€ 1 495 750,00
Address
Lazarettstrasse 36
80636 Munich
Germany

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Region
Bayern Oberbayern München, Kreisfreie Stadt
Activity type
Public bodies (excluding Research Organisations and Secondary or Higher Education Establishments)
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Total cost
€ 1 495 750,00

Beneficiaries (1)