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AstroSignals

Spatiotemporal dynamics of subcellular energy metabolism in astrocytes

Total Cost €

0

EC-Contrib. €

0

Partnership

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 AstroSignals project word cloud

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

architecture    pool    combining    compartmentalization    contributes    functional    expertise    surface    local    networks    glucose    opening    energetic    function    sirna    atp    source    generate    confocal    rapid    genetically    er    spatial    lumen    momentum    knockdown    sensors    unknown    organization    phosphatase    immunocytochemistry    regulation    requiring    transduction    optical    human    brain    pase    astrocytes    spatiotemporal    suggest    microdomains    fluorescence    signalling    encoded    cell    hypotheses    contains    emerged    biosensors    reflection    internal    initial    diseases    phosphate    signals    subcellular    locations    beta    microscopy    energetically    employ    luminal    link    meet    techniques    intracellular    reservoir    total    metabolic    tirf    provision    significance    transporter    receptors    sources    possibilities    cultured    pools    astrocytic    treatments    metabolism    transfer    cytosolic    cellular    gaining    energy    signal    transported    ca2   

Project "AstroSignals" data sheet

The following table provides information about the project.

Coordinator
THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE 

Organization address
address: TRINITY LANE THE OLD SCHOOLS
city: CAMBRIDGE
postcode: CB2 1TN
website: www.cam.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]
 Project website http://www.phar.cam.ac.uk/research/taylor/people
 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-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-04-01   to  2017-03-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    THE CHANCELLOR MASTERS AND SCHOLARSOF THE UNIVERSITY OF CAMBRIDGE UK (CAMBRIDGE) coordinator 183˙454.00

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 Project objective

The functional significance of subcellular compartmentalization in signal transduction has emerged in recent years, a development that is gaining momentum due to significant advances in optical microscopy and genetically encoded biosensors. However, much less attention has been given to the spatial architecture of the metabolic networks that provide energetic support for intracellular processes. This project will investigate spatiotemporal organization of energy metabolism in astrocytes, focusing on two hypotheses: • I propose that within astrocytes, signalling microdomains are energetically supported by local delivery of ATP. I will employ confocal and total internal reflection fluorescence (TIRF) microscopy, using biosensors for ATP, glucose and Ca2 that can be targeted to subcellular locations. My initial focus is on cultured human astrocytes and the provision of ATP for Ca2 signalling. Do the five cellular sources of astrocytic ATP support different ATP pools? Which pools are needed for the many ATP-requiring steps that link cell-surface receptors to Ca2 signals? • I suggest that the ER lumen may provide a glucose reservoir that allows rapid intracellular transfer of glucose to meet local energy needs. The ER of astrocytes contains luminal glucose-6-phosphatase-β (G-6-Pase-β) and a glucose-6-phosphate transporter, which together can generate an ER luminal pool of glucose. The source of glucose-6-phosphate transported into the ER and the function of luminal glucose are unknown. Using cytosolic and ER-targeted glucose sensors, immunocytochemistry and siRNA knockdown of glucose G-6-Pase-β, I will determine the source of the glucose pool and whether it contributes to metabolic support of Ca2 signals. Combining state-of-the-art techniques and expertise in the fields of cell signalling and metabolism, this project will enhance our understanding of metabolic regulation of signal transduction, opening new possibilities for targeted treatments of brain diseases.

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