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Exosomes

Regulated secretion and role of urinary nanovesicles

Total Cost €

0

EC-Contrib. €

0

Partnership

0

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 Exosomes project word cloud

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

microbiological    pathophysiological    fellowship    rates    bound    proteins    underlying    capacity    scientific    exosome    constituents    goals    freedom    quantitative    release    disciplines    biology    career    origin    secreted    variety    independently    combined    neurobiology    released    examine    proteomic    incl    portfolio    provides    antigen    gain    nanovesicles    implications    protein    tumor    bacteria    regulated    genetic    cargo    me    prospects    skills    extensive    proteomics    inhibit    exosomes    molecular    types    patients    roles    cell    intercellular    basis    presentation    combine    biological    vesicles    ideas    multiple    immunology    contain    secretion    materials    normal    collecting    transfer    stem    techniques    contributes    urinary    run    bioinformatics    immunity    transdisciplinary    unclear    pathogen    qualitative    int    give    collaborations    laboratory    renal    innate    profiling    samples    host    urine    small    lab    mechanisms    extracellular    membrane    communications   

Project "Exosomes" data sheet

The following table provides information about the project.

Coordinator
AARHUS UNIVERSITET 

Organization address
address: NORDRE RINGGADE 1
city: AARHUS C
postcode: 8000
website: www.au.dk

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 Denmark [DK]
 Project website http://interpret.au.dk/other-funded-research-projects/regulated-secretion-and-role-of-urinary-nanovesicles/
 Total cost 200˙194 €
 EC max contribution 200˙194 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2015
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2017
 Duration (year-month-day) from 2017-09-01   to  2019-08-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    AARHUS UNIVERSITET DK (AARHUS C) coordinator 200˙194.00

Map

 Project objective

Extracellular nanovesicles called “exosomes” are small membrane-bound vesicles that are secreted by a variety of cell types. Exosomes contain various molecular constituents of their cell of origin, incl. proteins and genetic materials. The exosome release pathway contributes towards protein secretion, antigen presentation and pathogen transfer and roles of exosomes in intercellular communications and transfer of materials have been studied in immunology, neurobiology, stem cell and tumor biology. Exosomes are also released into the urine, although their role in urine is unclear and provides the basis of this fellowship. To gain novel information about urinary exosomes, a transdisciplinary approach is required. I will use my current knowledge of qualitative and quantitative proteomics combined with extensive bioinformatics to study urinary and renal exosomes and their ‘cargo’ secreted under normal and pathophysiological conditions. I will combine this information with new ideas and techniques I will learn in my host laboratory to examine rates of exosome secretion and to assess whether exosomes have the capacity to inhibit the growth of bacteria. Methodologies in this fellowship include techniques which I have extensive experience of e.g. large scale proteomic profiling, and novel techniques that I will learn in the host lab to enhance my research portfolio and future career prospects, including cell biological and microbiological techniques and experience in collecting/using samples from patients. The scientific goals of the project are to investigate the underlying mechanisms for regulated exosome secretion and the role of exosomes in innate immunity. As exosomes are secreted from multiple cell types, this study will have major implications for a variety of biology disciplines. The fellowship will develop my career by providing new novel laboratory skills, it will give me greater freedom to independently run a research project and increase my int collaborations.

 Publications

year authors and title journal last update
List of publications.
2019 Qi Wu, Takwa S. Aroankins, Lei Cheng, Robert A. Fenton
SUMOylation Landscape of Renal Cortical Collecting Duct Cells
published pages: 3640-3648, ISSN: 1535-3893, DOI: 10.1021/acs.jproteome.9b00306
Journal of Proteome Research 18/10 2020-01-20
2018 Robert A. Fenton
Proteomic approaches in kidney disease biomarker discovery
published pages: F1817-F1821, ISSN: 1931-857X, DOI: 10.1152/ajprenal.00421.2018
American Journal of Physiology-Renal Physiology 315/6 2020-01-20
2019 Lei Cheng, Søren Brandt Poulsen, Qi Wu, Cristina Esteva-Font, Emma T. B. Olesen, Li Peng, Björn Olde, L. M. Fredrik Leeb-Lundberg, Trairak Pisitkun, Timo Rieg, Henrik Dimke, Robert A. Fenton
Rapid Aldosterone-Mediated Signaling in the DCT Increases Activity of the Thiazide-Sensitive NaCl Cotransporter
published pages: 1454-1470, ISSN: 1046-6673, DOI: 10.1681/asn.2018101025
Journal of the American Society of Nephrology 30/8 2020-01-20
2018 Qi Wu, Hanne B. Moeller, Donté A. Stevens, Rebekah Sanchez-Hodge, Gabrielle Childers, Marleen L.A. Kortenoeven, Lei Cheng, Lena L. Rosenbaek, Carrie Rubel, Cam Patterson, Trairak Pisitkun, Jonathan C. Schisler, Robert A. Fenton
CHIP Regulates Aquaporin-2 Quality Control and Body Water Homeostasis
published pages: ASN.2017050526, ISSN: 1046-6673, DOI: 10.1681/ASN.2017050526
Journal of the American Society of Nephrology 2020-01-20

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

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