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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.

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

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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