Skip to main content
European Commission logo
English English
CORDIS - EU research results

From mechanical stress to vascular fate

Project description

Understanding role of the mechanical environment in vascular remodelling

Cell phenotype and cell fate in the vascular system depend on the mechanical properties of the environment. Normal physiological mechanical conditions define and stabilise cell phenotype, while aberrant mechanical stress triggers phenotypic changes that lead to inflammation and vascular remodelling. The current hypothesis is that the transmission of mechanical stresses to the nucleus activates signalling pathways, thereby regulating gene expression. However, in contrast to most vascular cells, resident stem cells (RSCs) remain undifferentiated, despite the constant pressure of cyclic stretches. The ERC-funded MechanoFate project aims to determine the nuclear mechanotransduction pathways regulating phenotypic responses to mechanical stresses in vascular stresses and the molecular mechanisms protecting RSCs from stretch-induced differentiation.


In the vascular system, cell phenotype and fate are driven by the mechanical environment. Whereas physiological mechanical stress defines and stabilizes normal cell phenotype, aberrant mechanical signals trigger phenotypic alteration, leading to inflammation and vascular remodelling. Despite recent advances, how mechanical cues impact gene expression to specify cell phenotype remains poorly understood.
Our hypothesis is that mechanical stresses are transmitted to the nucleus where they activate signaling pathways, which in turn regulate gene expression, but what are these mechanotransduction mechanisms occurring within the nucleus? Besides, while most vascular cells respond to mechanical force, Resident Stem Cells (RSCs) are virtually insensitive and remain undifferentiated despite constant cyclic stretch. What are the molecular mechanisms which protect RSCs from stretch-induced differentiation?
To answer these questions, we designed an interdisciplinary proposal which gathers biophysical, biochemical and genetic assays, with the following objectives: I) To determine how nuclear mechanotransduction pathways regulate vascular cell phenotype in response to mechanical cues. By combining proteomic and biophysical assays, we will identify nuclear proteins that are post-translationally modified in response to mechanical stress, then we will determine their contribution to gene expression regulation and vascular cell differentiation. II) To identify the molecular mechanisms which protect RSCs from stretch-induced differentiation. We will identify differentially expressed force-bearing structural elements in RSCs compared to more differentiated vascular cells and we will evaluate their impact on gene expression, stress transmission, RSC differentiation and blood vessel formation.The proposed project will yield new insights in different areas of life science from cell biology to potential identification of new therapeutic targets in cardiovascular and regenerative medicine.

Host institution

Net EU contribution
€ 1 498 412,50
75654 Paris

See on map

Ile-de-France Ile-de-France Paris
Activity type
Research Organisations
Total cost
€ 1 498 412,50

Beneficiaries (1)