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ROMB SIGNED

Retina Organoid Mechanobiology

Total Cost €

0

EC-Contrib. €

0

Partnership

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 ROMB project word cloud

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

neuroscience    vitro    disease    hereby    door    cells    biophysical    mimic    promises    engineering    me    genetic    physicists    limited    interactions    aggregates    prevented    model    tailoring    posts    manipulate    variations    guide    turn    suited    retina    stem    organoid    plan    actuators    functional    techniques    shape    opening    organogenesis    exists    diseases    introduces    final    modeling    first    accordingly    mouse    revealed    reveal    physiological    retinas    detect    ball    gene    bioengineers    lightsheet    abnormalities    quantify    romb    hallmark    mechanobiology    tissue    onset    organization    mechanics    peptide    cell    ferrofluid    readout    cellular    mechanical    court    3d    signals    physical    cross    app    players    quantified    multifaceted    recorded    basic    glaucoma    tackle    droplets    uniquely    mutation    building    organoids    neuronal    opens    signatures    mechanically    establishment    microscopy    alzheimer    breakthrough    linked    environment    function    disciplinary    behavior    regulating    carries   

Project "ROMB" data sheet

The following table provides information about the project.

Coordinator
LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN 

Organization address
address: GESCHWISTER SCHOLL PLATZ 1
city: MUENCHEN
postcode: 80539
website: www.uni-muenchen.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 1˙497˙175 €
 EC max contribution 1˙497˙175 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-STG
 Funding Scheme ERC-STG
 Starting year 2020
 Duration (year-month-day) from 2020-09-01   to  2025-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    LUDWIG-MAXIMILIANS-UNIVERSITAET MUENCHEN DE (MUENCHEN) coordinator 1˙497˙175.00

Map

 Project objective

The retina carries signatures of neuronal diseases which have been linked to mechanical abnormalities, including Glaucoma and Alzheimer’s disease. Yet no biophysical retina model exists due to a cross-disciplinary challenge: While stem cell derived organoids mimic the retina in vitro, organoid research has been limited by large variations in cell and tissue organization. Mechanobiology, in turn, has revealed mechanical signals as essential players in regulating cellular behavior to guide organogenesis. Accordingly, the ball is in the court of physicists and bioengineers to quantify those mechanical signals and shape tissue growth by tailoring the physical interactions of cells with their environment. Finally, the functionality of the retina has to be quantified via neuroscience techniques. This multifaceted challenge has prevented the establishment of the retina organoid as a biophysical model. ROMB introduces a biophysical model for the retina which I will use to model Alzheimer’s disease in vitro. It will be built on 4 cross-disciplinary posts: (i) retina organoids as a physiological in vitro model, (ii) tissue mechanics measurements, (iii) neuronal activity readout and (iv) disease modeling. First, I will reveal the mechanical building plan of retina organoids using ferrofluid droplets as mechanical actuators, hereby opening the field of organoid mechanobiology. In a second step, the organoid’s 3D neuronal function will be recorded using lightsheet microscopy. Mechanical, functional and genetic access will allow me in a final step to detect and manipulate Alzheimer’s disease: using mouse retina organoids with a mutation in the App gene, I will mechanically characterize the formation of those peptide aggregates which are the hallmark of disease onset. ROMB opens the door to engineering functional retinas in vitro. Moreover, it will be uniquely suited to tackle mechanically related neuronal diseases and promises a breakthrough for basic and applied research.

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

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