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STRomA SIGNED

Novel Matrix Stiffness-regulated Genes in Lymphangiogenesis and Angiogenesis

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 STRomA project word cloud

Explore the words cloud of the STRomA project. It provides you a very rough idea of what is the project "STRomA" about.

surrounding    mechanotransduction    time    understand    signaling    extracellular    adhesions    predominantly    dynamics    similarly    fundamentally    regulatory    generate    modulate    ecm    ec    ecs    composition    visualize    hypothesize    microscope    imaging    diseases    sensor    bec    controls    angiogenesis    vessel    blood    cytoskeletal    preliminary    forces    endothelial    treatment    intracellular    lymphatic    differently    translate    tissues    regulated    rna    matrices    independent    pivotal    sequencing    stiffness    3200    vitro    angiogenic    shown    mechanism    leader    mechanical    significantly    lecs    cultured    performed    cgmp    techniques    stimuli    differ    implications    disease    becs    analyze    biological    models    family    interestingly    transgenic    differential    genes    fluorescent    me    tree    live    group    mouse    protein    molecule    edema    suggesting    cell    soft    inside    stiff    lymph    ultimately    last    regulating    physical    recognize    lymphangiogenesis    actin    first    vascular    matrix    action    cells    integrally   

Project "STRomA" data sheet

The following table provides information about the project.

Coordinator
UNIVERSITAETSKLINIKUM HAMBURG-EPPENDORF 

Organization address
address: Martinistrasse 52
city: HAMBURG
postcode: 20251
website: www.uke.uni-hamburg.de

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Germany [DE]
 Total cost 162˙806 €
 EC max contribution 162˙806 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2018
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2019
 Duration (year-month-day) from 2019-10-01   to  2021-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    UNIVERSITAETSKLINIKUM HAMBURG-EPPENDORF DE (HAMBURG) coordinator 162˙806.00

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 Project objective

Endothelial cells (ECs) recognize and respond to mechanical forces through their cell-cell and cell-matrix adhesions and translate physical stimuli into biological responses in a process called mechanotransduction. The composition and mechanical properties of the extracellular matrix (ECM) differ across the vascular tree, in its surrounding tissues and in development and diseases, such as edema formation. I have recently shown for the first time that ECM stiffness fundamentally controls lymphangiogenesis. I hypothesize that changes in ECM stiffness are a key regulatory mechanism of angiogenic processes in development and disease. A comprehensive analysis of novel ECM stiffness-regulated genes is pivotal to understand these processes integrally. In a preliminary study, I have performed differential RNA sequencing of blood (B) and lymphatic (L) ECs cultured on soft and stiff matrices. 3200 genes were regulated similarly in BECs and LECs in response to changes in matrix stiffness. Interestingly, the same number of genes was differently regulated. In the next two years, I will study the role of selected genes in lymphangiogenesis and angiogenesis in vitro and in transgenic mouse models with state-of-the-art microscope and live imaging techniques. First, I will analyze an actin-regulating protein family that is significantly regulated by matrix stiffness in both, BEC and LECs, suggesting a more general role in lymphangiogenesis and angiogenesis by regulating cytoskeletal dynamics. Second, I will study a molecule, which is involved in intracellular cGMP signaling and is predominantly regulated in LECs, suggesting a more specific role in lymphangiogenesis. Last, I will generate an in vitro fluorescent stiffness sensor to live-visualize changes in stiffness inside the EC. Ultimately, the proposed action can provide novel targets to modulate lymph and blood vessel formation with implications for edema treatment and will support me to become an independent group leader.

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The information about "STROMA" are provided by the European Opendata Portal: CORDIS opendata.

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