Opendata, web and dolomites

ELECTRO NEEDLE SIGNED

In situ stem cell monitoring system based on conductive nanoneedle devices for tracking cell fates in invasive manner

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 ELECTRO NEEDLE project word cloud

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

vivo    published    expecting    guiding    culture    solid    stevens    risk    endogenous    mater    neural    seong    hyejeong    immunoassay    electronic    instead    migration    vitro    prone    modifiable    critical    cure    solutions    fate    periods    buffer    mscs    decade    porous    capacity    damage    2017    proving    sensors    transplanted    newly    condensation    cells    nerve    thanks    longer    ratio    framework    investigation    degradable    tracking    membrane    multilineage    morphologies    re    difficulty    remarkably    source    silicon    assayed    manipulating    biological    invasive    drawing    ideal    2015    disorders    group    nns    nuclear    provides    march    conductive    college    self    ethical    media    monitoring    stem    48    nucleus    version    joining    teratoma    capacities    acs    byintegrating    stimulating    imperial    hrs    stability    receptors    therapies    nanoneedles    exhibited    limited    dr    2000    suitability    cell    london    cytotoxic    mesenchymal    ipscs    pluripotent    differentiation    nat    nano    detecting    manipulation    psi    icl    renewal    proper    penetrate   

Project "ELECTRO NEEDLE" data sheet

The following table provides information about the project.

Coordinator
IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE 

Organization address
address: SOUTH KENSINGTON CAMPUS EXHIBITION ROAD
city: LONDON
postcode: SW7 2AZ
website: http://www.imperial.ac.uk/

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 United Kingdom [UK]
 Total cost 183˙454 €
 EC max contribution 183˙454 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-10-01   to  2020-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    IMPERIAL COLLEGE OF SCIENCE TECHNOLOGY AND MEDICINE UK (LONDON) coordinator 183˙454.00

Map

 Project objective

Stem cell-based therapies to cure nerve system disorders using the self-renewal and multilineage differentiation capacities of the transplanted stem cells have been drawing attention during the past decade. Especially, differentiation of mesenchymal stem cells (MSCs) and induced pluripotent stem cells (iPSCs) into neural cells are especially investigated since early 2000’s, thanks to their being much less prone to the ethical issues and the risk of developing teratoma. However, the critical challenges are the difficulty in: (i) guiding their proper differentiation to neural cells, and (ii) tracking their fate, distribution, and migration due to the limited tracking methods. In 2015, the Stevens Group at Imperial College London (ICL) developed high-aspect ratio, porous silicon nanoneedles (pSi nNs) for in vitro and in vivo manipulation of cell behaviour. Remarkably, the nNs penetrate the cell membrane but do not damage the nucleus, instead stimulating nuclear condensation (Published in Nat. Mater., ACS Nano, etc.). However, current nNs in the Stevens Group is degradable within 48 hrs which is not ideal for long-term biological studies, especially for detecting/monitoring the cell differentiation during the culture. Recently, the applicant (Dr Hyejeong Seong) newly developed non-porous, solid version of nNs after her joining to the Stevens Group in March 2017. The new nNs exhibited a high stability in cell culture media and buffer solutions, proving their suitability for long-term investigation of cell fate. This provides an ideal framework for manipulating and exploiting cell behaviour for longer periods as a means for understanding differentiation capacity of this promising stem cell source. Furthermore, we’re expecting that the new nNs are modifiable as conductive electronic sensors, byintegrating new nNs with non-cytotoxic electronic devices. Through these devices, cell morphologies and endogenous receptors, will be assayed without invasive immunoassay.

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "ELECTRO NEEDLE" project.

For instance: the website url (it has not provided by EU-opendata yet), the logo, a more detailed description of the project (in plain text as a rtf file or a word file), some pictures (as picture files, not embedded into any word file), twitter account, linkedin page, etc.

Send me an  email (fabio@fabiodisconzi.com) and I put them in your project's page as son as possible.

Thanks. And then put a link of this page into your project's website.

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

More projects from the same programme (H2020-EU.1.3.2.)

MY MITOCOMPLEX (2021)

Functional relevance of mitochondrial supercomplex assembly in myeloid cells

Read More  

CYBERSECURITY (2018)

Cyber Security Behaviours

Read More  

LUNG-BIM (2019)

Induction of B cell immunity in the lung mucosa

Read More