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aCROBAT SIGNED

Circadian Regulation Of Brown Adipose Thermogenesis

Total Cost €

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EC-Contrib. €

0

Partnership

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 aCROBAT project word cloud

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

orchestrate    small    mass    transcriptional    edge    unlock    strategies    cues    burning    circadian    incorporates    oscillations    unappreciated    thermogenic    vivo    therapeutic    diabetes    abrupt    coordinately    signaling    calorie    validations    primary    source    critically    stress    group    cutting    rna    question    link    newly    rhythm    rhythms    energy    metabolic    crosstalk    drive    customized    maintaining    evolutionary    additionally    framework    pharmacological    mammals    enzymes    reached    heat    models    gain    neuronal    mouse    previously    diseases    bat    direct    effectors    input    harness    shape    conserved    hormonal    candidates    cell    treatment    possesses    demand    functions    spectrometry    anticipation    nutrient    insights    expending    blood    pandemic    environmental    facets    network    receptors    phenotyping    proportions    function    reveal    bioenergetic    discovered    obesity    combating    adipose    mechanistic    capacity    constraints    translational    metabolism    prevention    humans    tissue    brown    regulation    extend    daily    physiological    preliminary    dissipating    vitro    sequencing    borne    fundamental    networks    generation    surface    yielded    adapt   

Project "aCROBAT" data sheet

The following table provides information about the project.

Coordinator
KOBENHAVNS UNIVERSITET 

Organization address
address: NORREGADE 10
city: KOBENHAVN
postcode: 1165
website: www.ku.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]
 Total cost 1˙497˙007 €
 EC max contribution 1˙497˙007 € (100%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2014-STG
 Funding Scheme ERC-STG
 Starting year 2015
 Duration (year-month-day) from 2015-05-01   to  2020-04-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    KOBENHAVNS UNIVERSITET DK (KOBENHAVN) coordinator 1˙497˙007.00

Map

 Project objective

Obesity and diabetes have reached pandemic proportions and new therapeutic strategies are critically needed. Brown adipose tissue (BAT), a major source of heat production, possesses significant energy-dissipating capacity and therefore represents a promising target to use in combating these diseases. Recently, I discovered a novel link between circadian rhythm and thermogenic stress in the control of the conserved, calorie-burning functions of BAT. Circadian and thermogenic signaling to BAT incorporates blood-borne hormonal and nutrient cues with direct neuronal input. Yet how these responses coordinately shape BAT energy-expending potential through the regulation of cell surface receptors, metabolic enzymes, and transcriptional effectors is still not understood. My primary goal is to investigate this previously unappreciated network of crosstalk that allows mammals to effectively orchestrate daily rhythms in BAT metabolism, while maintaining their ability to adapt to abrupt changes in energy demand. My group will address this question using gain and loss-of-function in vitro and in vivo studies, newly-generated mouse models, customized physiological phenotyping, and cutting-edge advances in next generation RNA sequencing and mass spectrometry. Preliminary, small-scale validations of our methodologies have already yielded a number of novel candidates that may drive key facets of BAT metabolism. Additionally, we will extend our circadian and thermogenic studies into humans to evaluate the translational potential. Our results will advance the fundamental understanding of how daily oscillations in bioenergetic networks establish a framework for the anticipation of and adaptation to environmental challenges. Importantly, we expect that these mechanistic insights will reveal pharmacological targets through which we can unlock evolutionary constraints and harness the energy-expending potential of BAT for the prevention and treatment of obesity and diabetes.

 Publications

year authors and title journal last update
List of publications.
2018 Elahu G. Sustarsic, Tao Ma, Matthew D. Lynes, Michael Larsen, Iuliia Karavaeva, Jesper F. Havelund, Carsten H. Nielsen, Mark P. Jedrychowski, Marta Moreno-Torres, Morten Lundh, Kaja Plucinska, Naja Z. Jespersen, Trisha J. Grevengoed, Barbara Kramar, Julia Peics, Jakob B. Hansen, Farnaz Shamsi, Isabel Forss, Ditte Neess, Susanne Keipert, Jianing Wang, Katharina Stohlmann, Ivan Brandslund, Cramer Christensen, Marit E. Jørgensen, Allan Linneberg, Oluf Pedersen, Michael A. Kiebish, Klaus Qvortrup, Xianlin Han, Bente Klarlund Pedersen, Martin Jastroch, Susanne Mandrup, Andreas Kjær, Steven P. Gygi, Torben Hansen, Matthew P. Gillum, Niels Grarup, Brice Emanuelli, Søren Nielsen, Camilla Scheele, Yu-Hua Tseng, Nils J. Færgeman, Zachary Gerhart-Hines
Cardiolipin Synthesis in Brown and Beige Fat Mitochondria Is Essential for Systemic Energy Homeostasis
published pages: , ISSN: 1550-4131, DOI: 10.1016/j.cmet.2018.05.003
Cell Metabolism 2019-05-29

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