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STRELECOID SIGNED

Stretchable mesh-electrodes interfacing human iPSC brain organoids

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 STRELECOID project word cloud

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

plasticity    invaluable    parkinson    preparations    limitation    mesh    developmental    opens    mean    tissue    correct    inaccessible    alzheimer    overcome    sensory    combination    animal    lack    vitro    organoids    electrodes    physiological    cells    variety    elicit    model    seamlessly    parallel    humans    cellular    single    genetic    cortical    mental    successful    recent    psychiatric    performed    bear    cell    signature    transcriptomics    donor    poorly    models    operate    engineering    overwhelmingly    thereby    skin    input    translate    epilepsy    assemble    maturation    cultures    code    neurons    efforts    brain    human    symbiotically    donors    clinical    ensembles    thalamic    massively    disease    animals    borne    male    whereby    stages    faithful    precisely    electric    culture    proximity    light    neural    recruit    advantages    shape    sexes    anatomically    disorders    integrate    grows    shed    stem    neurosphere    pluripotent    functional    ipsc    regions    patient    environment    possibility    nervous    genome    reprogram    integrating    unprecedented    form    3d    central    biomaterials    assembloids    expand    refined    neurospheres    arrangements    plan    self   

Project "STRELECOID" data sheet

The following table provides information about the project.

Coordinator
FONDAZIONE ISTITUTO ITALIANO DI TECNOLOGIA 

Organization address
address: VIA MOREGO 30
city: GENOVA
postcode: 16163
website: www.iit.it

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 Italy [IT]
 Total cost 251˙002 €
 EC max contribution 251˙002 € (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-GF
 Starting year 2019
 Duration (year-month-day) from 2019-12-01   to  2022-11-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FONDAZIONE ISTITUTO ITALIANO DI TECNOLOGIA IT (GENOVA) coordinator 251˙002.00
2    BOARD OF TRUSTEES OF THE LELAND STANFORD JUNIOR UNIVERSITY US (STANFORD) partner 0.00

Map

 Project objective

Recent advances in cellular engineering allow to recruit skin cells from donors and reprogram them into neural stem cells. These induced pluripotent stem cells (iPSC) bear the genetic code of the human patient. Efforts to culture these cells in-vitro have been successful in creating a wide variety of 3D arrangements called neurospheres. Because the human central nervous system is by and large inaccessible at all developmental stages, these functional tissue preparations are invaluable. Furthermore, clinical studies performed in animal models are known to translate poorly to humans and therefore these systems provide unprecedented advantages: human neurons in a controlled environment that have the genetic signature of psychiatric or mental disorders borne by the donor patient, such as Alzheimer’s or Parkinson’s disease. Finally, compared to animal studies where overwhelmingly only male animals are studied, stem cell research can operate on both sexes. The combination of new biomaterials, genome engineering and massively parallel single-cell transcriptomics opens opportunities to precisely study human brain disease A new exciting development is the possibility to form so-called assembloids, whereby organoids of different brain regions, as for example cortical and thalamic neural ensembles, are brought in proximity and self-assemble into anatomically correct brain regions. These approaches are necessary to study disorders like epilepsy. However these cultures lack physiological sensory input which are key in the development of mental plasticity. Here we plan to overcome this limitation by integrating new mesh-based electrodes that integrate seamlessly into brain tissue and expand symbiotically with the neurosphere as it grows, and thereby have a spatially refined mean to measure but also elicit neural activity. This will shed light on how electric maturation of these neurospheres comes about and help shape them to an anatomically more faithful brain model.

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

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