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EnBioN SIGNED

Engineering the Biointerface of Nanowires to Direct Stem Cell Differentiation

Total Cost €

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EC-Contrib. €

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Partnership

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 EnBioN project word cloud

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

signalling    strategies    mechanisms    localized    unexplored    nanostructures    mechanosensory    cellular    stimulation    nanowire    reprogramming    intracellular    dynamic    combining    cell    therapy    unknown    arrays    rational    platform    evident    regulatory    guide    multiple    manipulation    regenerative    niche    elusive    fate    medicine    direct    free    transfection    localize    interface    vector    broad    relies    timeliness    regeneration    microenvironment    undeveloped    arising    technologies    nanomaterials    organelles    interaction    debated    cells    largely    resolution    environment    directing    stem    stimuli    integrate    critical    biointerface    induce    nanowires    degree    sensing    highlights    principles    ratio    epigenetic    efficient    gene    enbion    differentiation    ing    tools    governing    tissue    engineer    membrane    ensue    guidelines    permeability    vertical    lengthscale    thanks    biological    highlighted    integrating    despite    engineering   

Project "EnBioN" data sheet

The following table provides information about the project.

Coordinator
KING'S COLLEGE LONDON 

Organization address
address: STRAND
city: LONDON
postcode: WC2R 2LS
website: www.kcl.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 1˙495˙430 €
 EC max contribution 1˙495˙430 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-STG
 Funding Scheme ERC-STG
 Starting year 2018
 Duration (year-month-day) from 2018-02-01   to  2023-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KING'S COLLEGE LONDON UK (LONDON) coordinator 1˙495˙430.00

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 Project objective

ENBION will engineer a platform to direct the differentiation of stem cells by developing principles for the rational design of the biointerface of nanowires. It is increasingly evident that efficient tissue regeneration can only ensue from combining the regenerative potential of stem cells with regulatory stimuli from gene therapy and niche engineering. Yet, despite significant advances towards integrating these technologies, the necessary degree of control over cell fate remains elusive. Vertical arrays of high aspect ratio nanostructures (nanowires) are rapidly emerging as promising tools to direct cell fate. Thanks to their unique biointerface, nanowires enable gene delivery, intracellular sensing, and direct stimulation of signalling pathways, achieving dynamic manipulation of cells and their environment. This broad manipulation potential highlights the importance and timeliness of engineering nanowires for regenerative medicine. However, developing a nanowire platform to direct stem cell fate requires design principles based on the largely unknown biological processes governing their interaction with cells. Enabling localized, vector-free gene therapy through efficient transfection relies on understanding the still debated mechanisms by which nanowires induce membrane permeability. Directing cell reprogramming requires understanding the largely unexplored mechanosensory processes and the resulting epigenetic effects arising from the direct interaction of nanowires with multiple organelles within the cell. Engineering the cell microenvironment requires yet undeveloped strategies to localize signalling and transfection with a resolution comparable to the lengthscale of cells. ENBION will develop this critical knowledge and integrate it into guidelines for dynamic manipulation of cells. Beyond the nanowire platform, the principles highlighted by this unique interface can guide the development of nanomaterials with improved control over cellular processes.

 Publications

year authors and title journal last update
List of publications.
2019 Valentina Onesto, William B. Barrell, Mary Okesola, Francesco Amato, Francesco Gentile, Karen J. Liu, Ciro Chiappini
A quantitative approach for determining the role of geometrical constraints when shaping mesenchymal condensations
published pages: , ISSN: 1387-2176, DOI: 10.1007/s10544-019-0390-0
Biomedical Microdevices 21/2 2019-10-01
2019 Sebastiaan Zijl, Aliaksei S. Vasilevich, Priyalakshmi Viswanathan, Ayelen Luna Helling, Nick R.M. Beijer, Gernot Walko, Ciro Chiappini, Jan de Boer, Fiona M. Watt
Micro-scaled topographies direct differentiation of human epidermal stem cells
published pages: 133-145, ISSN: 1742-7061, DOI: 10.1016/j.actbio.2018.12.003
Acta Biomaterialia 84 2019-10-01
2019 Sahana Gopal, Ciro Chiappini, James P. K. Armstrong, Qu Chen, Andrea Serio, Chia-Chen Hsu, Christoph Meinert, Travis J. Klein, Dietmar W. Hutmacher, Stephen Rothery, Molly M. Stevens
Immunogold FIB-SEM: Combining Volumetric Ultrastructure Visualization with 3D Biomolecular Analysis to Dissect Cell-Environment Interactions
published pages: 1900488, ISSN: 0935-9648, DOI: 10.1002/adma.201900488
Advanced Materials 31/32 2019-10-01
2019 Catherine S. Hansel, Spencer W. Crowder, Samuel Cooper, Sahana Gopal, Maria João Pardelha da Cruz, Leonardo de Oliveira Martins, Debora Keller, Stephen Rothery, Michele Becce, Anthony E. G. Cass, Chris Bakal, Ciro Chiappini, Molly M. Stevens
Nanoneedle-Mediated Stimulation of Cell Mechanotransduction Machinery
published pages: 2913-2926, ISSN: 1936-0851, DOI: 10.1021/acsnano.8b06998
ACS Nano 13/3 2019-10-01
2019 Sahana Gopal, Ciro Chiappini, Jelle Penders, Vincent Leonardo, Hyejeong Seong, Stephen Rothery, Yuri Korchev, Andrew Shevchuk, Molly M. Stevens
Porous Silicon Nanoneedles Modulate Endocytosis to Deliver Biological Payloads
published pages: 1806788, ISSN: 0935-9648, DOI: 10.1002/adma.201806788
Advanced Materials 31/12 2019-10-01

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