A fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion

The mechanisms by which organisms adapt their growth according to the availability of oxygen are incompletely understood. Here the authors identify the D rosophila fat body as a tissue regulating growth in response to oxygen sensing via a mechanism involving Hph inhibition, HIF1-a activation and ins...

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Main Authors: Michael J. Texada, Anne F. Jørgensen, Christian F. Christensen, Takashi Koyama, Alina Malita, Daniel K. Smith, Dylan F. M. Marple, E. Thomas Danielsen, Sine K. Petersen, Jakob L. Hansen, Kenneth A. Halberg, Kim F. Rewitz
Format: Article
Language:English
Published: Nature Publishing Group 2019-04-01
Series:Nature Communications
Online Access:https://doi.org/10.1038/s41467-019-09943-y
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spelling doaj-eb1d36697d6243149fc5a3d90944c2022021-05-11T12:15:58ZengNature Publishing GroupNature Communications2041-17232019-04-0110111610.1038/s41467-019-09943-yA fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretionMichael J. Texada0Anne F. Jørgensen1Christian F. Christensen2Takashi Koyama3Alina Malita4Daniel K. Smith5Dylan F. M. Marple6E. Thomas Danielsen7Sine K. Petersen8Jakob L. Hansen9Kenneth A. Halberg10Kim F. Rewitz11Department of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenCardiovascular Research, Department number 5377, Novo Nordisk A/SDepartment of Biology, University of CopenhagenDepartment of Biology, University of CopenhagenThe mechanisms by which organisms adapt their growth according to the availability of oxygen are incompletely understood. Here the authors identify the D rosophila fat body as a tissue regulating growth in response to oxygen sensing via a mechanism involving Hph inhibition, HIF1-a activation and insulin secretion.https://doi.org/10.1038/s41467-019-09943-y
collection DOAJ
language English
format Article
sources DOAJ
author Michael J. Texada
Anne F. Jørgensen
Christian F. Christensen
Takashi Koyama
Alina Malita
Daniel K. Smith
Dylan F. M. Marple
E. Thomas Danielsen
Sine K. Petersen
Jakob L. Hansen
Kenneth A. Halberg
Kim F. Rewitz
spellingShingle Michael J. Texada
Anne F. Jørgensen
Christian F. Christensen
Takashi Koyama
Alina Malita
Daniel K. Smith
Dylan F. M. Marple
E. Thomas Danielsen
Sine K. Petersen
Jakob L. Hansen
Kenneth A. Halberg
Kim F. Rewitz
A fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion
Nature Communications
author_facet Michael J. Texada
Anne F. Jørgensen
Christian F. Christensen
Takashi Koyama
Alina Malita
Daniel K. Smith
Dylan F. M. Marple
E. Thomas Danielsen
Sine K. Petersen
Jakob L. Hansen
Kenneth A. Halberg
Kim F. Rewitz
author_sort Michael J. Texada
title A fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion
title_short A fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion
title_full A fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion
title_fullStr A fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion
title_full_unstemmed A fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion
title_sort fat-tissue sensor couples growth to oxygen availability by remotely controlling insulin secretion
publisher Nature Publishing Group
series Nature Communications
issn 2041-1723
publishDate 2019-04-01
description The mechanisms by which organisms adapt their growth according to the availability of oxygen are incompletely understood. Here the authors identify the D rosophila fat body as a tissue regulating growth in response to oxygen sensing via a mechanism involving Hph inhibition, HIF1-a activation and insulin secretion.
url https://doi.org/10.1038/s41467-019-09943-y
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