Opendata, web and dolomites

MicroAdiPSChip SIGNED

Micro-Fat Tissue on Chip

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 MicroAdiPSChip project word cloud

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

metabolically    understand    inducible    tissues    metabolic    maintenance    brown    longer    attractive    activate    laboratory    white    heat    experimental    differentiation    obesity    lack    dynamically    data    combine    recapitulating    microenvironmental    nbsp    single    hipscs    incorporated    micrometers    store    restore    times    simulate    acquired    reserve    bioprinting    microfluidic    energy    mechanistically    intake    stem    clinical    obstacles    disorders    cold    diabetes    strategy    niches    leads    sizes    chip    of    cell    divided    serve    exploited    microenvironment    adipose    mechanical    imbalance    pluripotent    clinically    outside    differentiate    integration    architectural    expenditure    induce    resolution    exposure    cells    generate    technologies    detection    situ    mobilize    cures    mature    subtypes    active    tissue    treat    whereas    burn    fat    micro    natural    reveal    treatments    expansion    patient    adipocytes    beige    models    assembly    human    organisms    platforms    niche    chemical   

Project "MicroAdiPSChip" data sheet

The following table provides information about the project.

Coordinator
HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH 

Organization address
address: INGOLSTADTER LANDSTRASSE 1
city: NEUHERBERG
postcode: 85764
website: www.helmholtz-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˙775˙000 €
 EC max contribution 1˙775˙000 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2017-COG
 Funding Scheme ERC-COG
 Starting year 2018
 Duration (year-month-day) from 2018-06-01   to  2023-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    HELMHOLTZ ZENTRUM MUENCHEN DEUTSCHES FORSCHUNGSZENTRUM FUER GESUNDHEIT UND UMWELT GMBH DE (NEUHERBERG) coordinator 1˙775˙000.00

Map

 Project objective

Human fat tissue has evolved to serve as a major energy reserve. An imbalance between energy intake and expenditure leads to an expansion of adipose tissue. Maintenance of this energy imbalance over longer times leads to obesity and metabolic disorders such as type 2 diabetes, for which clinical cures are not yet available. Adipocytes are the main cell type within the adipose tissue and can be divided into white, beige, and brown subtypes. White adipocytes store and mobilize energy, whereas beige and brown adipocytes store and burn energy during cold exposure to generate heat. An attractive strategy to restore the energy imbalance and treat obesity is to activate or increase the number of beige adipocytes in white adipose tissue. The main research obstacles affecting our ability to induce beige adipocytes is our lack of laboratory test systems recapitulating the microenvironmental conditions of the adipose tissue. Therefore, this research project aims to develop adipose tissue models outside organisms in sizes of micrometers for studying the differentiation of human inducible pluripotent stem cells (hiPSCs) into mature adipocytes. For assembly of the micro-fat tissues, we combine microfluidic and bioprinting technologies. In particular, the integration of micro-fat tissue on microfluidic chip platforms will be exploited to dynamically control the chemical, cell architectural, and mechanical microenvironment of hiPSCs incorporated in the micro-fat tissue. With novel single-cell-resolution in situ detection systems, we will aim to reveal, which microenvironmental stem cell niche factors are required to differentiate hiPSCs into metabolically active beige adipocytes. The acquired experimental data will help to mechanistically understand the role of natural stem cell niches, determine how to simulate them under laboratory conditions and finally provide patient-specific, clinically relevant information for developing new cell-based treatments for obesity.

 Publications

year authors and title journal last update
List of publications.
2020 Julius Wiener, Daniel Kokotek, Simon Rosowski, Heiko Lickert, Matthias Meier
Preparation of single- and double-oligonucleotide antibody conjugates and their application for protein analytics
published pages: , ISSN: 2045-2322, DOI: 10.1038/s41598-020-58238-6
Scientific Reports 10/1 2020-02-05

Are you the coordinator (or a participant) of this project? Plaese send me more information about the "MICROADIPSCHIP" 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 "MICROADIPSCHIP" are provided by the European Opendata Portal: CORDIS opendata.

More projects from the same programme (H2020-EU.1.1.)

CohoSing (2019)

Cohomology and Singularities

Read More  

CHIPTRANSFORM (2018)

On-chip optical communication with transformation optics

Read More  

CoolNanoDrop (2019)

Self-Emulsification Route to NanoEmulsions by Cooling of Industrially Relevant Compounds

Read More