Evidence map›Paper›PMID 32663458›Full record

ArticleCell metabolism2020

PHD3 Loss Promotes Exercise Capacity and Fat Oxidation in Skeletal Muscle.

Haejin Yoon, Jessica B Spinelli, Elma Zaganjor, Samantha J Wong, Natalie J German, Elizabeth C Randall, Afsah Dean, Allen Clermont, Joao A Paulo, Daniel Garcia and 8 more

Open access · bronzeAbstract read
In one paragraph

Article in Cell metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
2.5field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

23 citing papers in PubMed, 33 citations in OpenAlex.

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  19. The effect of HIF on metabolism and immunity.Nature reviews. Nephrology · 2022
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

18 authors at 5 institutions in 2 countries.

Haejin YoonDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Jessica B SpinelliDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Elma ZaganjorDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Samantha J WongDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Natalie J GermanDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Elizabeth C RandallDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, Boston, MA, USA.
Afsah DeanSection on Integrative Physiology and Metabolism, Joslin Diabetes Center, Boston, MA, USA.
Allen ClermontSection on Integrative Physiology and Metabolism, Joslin Diabetes Center, Boston, MA, USA.
Joao A PauloDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Daniel GarciaThe Salk Institute for Biological Studies, 10010 N. Torrey Pines Road, La Jolla, CA, USA.
Hao LiLaboratory of Integrative and Systems Physiology, École Polytechnique Fédérale de Lausanne, Lausanne 1015, Switzerland.
Olivia RomboldDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Nathalie Y R AgarDepartment of Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, Boston, MA, USA; Departments of Neurosurgery and Cancer Biology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; Dana-Farber Cancer Institute, Harvard Medical School, Boston, MA, USA.
Laurie J GoodyearSection on Integrative Physiology and Metabolism, Joslin Diabetes Center, Boston, MA, USA.
Reuben J ShawThe Salk Institute for Biological Studies, 10010 N. Torrey Pines Road, La Jolla, CA, USA.
Steven P GygiDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA.
Johan AuwerxLaboratory of Integrative and Systems Physiology, École Polytechnique Fédérale de Lausanne, Lausanne 1015, Switzerland.
Marcia C HaigisDepartment of Cell Biology, Blavatnik Institute, Harvard Medical School, Boston, MA, USA. Electronic address: marcia_haigis@hms.harvard.edu.
Harvard University · USJoslin Diabetes Center · USBrigham and Women's Hospital · USÉcole Polytechnique Fédérale de Lausanne · CHSalk Institute for Biological Studies · US

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI Alessandro Doria · 1986 to 2026
$50.5M
Image Guided Therapy Center - Ultrasound-based sensor system for the monitoring of COVID-19 patientsP41EB015898 · NIBIB · BRIGHAM AND WOMEN'S HOSPITAL · PI TEMPANY, CLARE M · 2012 to 2021
$18.9M
New Sample Multiplexing Technologies to Identify Chemical Probes and Illuminate Ubiquitin BiologyR01GM067945 · NIGMS · HARVARD UNIVERSITY (MEDICAL SCHOOL) · PI GYGI, STEVEN P · 2003 to 2024
$10.5M
Multidisciplinary Training in Image-Guided TherapyR25CA089017 · NCI · BRIGHAM AND WOMEN'S HOSPITAL · PI FENNESSY, FIONA · 2001 to 2017
$7.8M
Molecular mechanisms of Nutrient sensing in cancerR01CA213062 · NCI · HARVARD MEDICAL SCHOOL · PI HAIGIS, MARCIA · 2017 to 2021
$1.9M
Metabolic Recycling and Compartmentalization in Tumor ProgressionK00CA234839 · NCI · WHITEHEAD INSTITUTE FOR BIOMEDICAL RES · PI SPINELLI, JESSICA BROOKE · 2019 to 2022
$394k
Metabolic Recycling and Compartmentalization in Tumor ProgressionF99CA234839 · NCI · HARVARD UNIVERSITY · PI SPINELLI, JESSICA BROOKE · 2018 to 2018
$35k
NCI NIH HHS F99 CA234839NCI NIH HHS K00 CA234839NCI NIH HHS R01 CA213062NCI NIH HHS R25 CA089017NIBIB NIH HHS P41 EB015898NIDDK NIH HHS P30 DK036836NIGMS NIH HHS R01 GM067945
6 · The paper itself

Abstract

Rapid alterations in cellular metabolism allow tissues to maintain homeostasis during changes in energy availability. The central metabolic regulator acetyl-CoA carboxylase 2 (ACC2) is robustly phosphorylated during cellular energy stress by AMP-activated protein kinase (AMPK) to relieve its suppression of fat oxidation. While ACC2 can also be hydroxylated by prolyl hydroxylase 3 (PHD3), the physiological consequence thereof is poorly understood. We find that ACC2 phosphorylation and hydroxylation occur in an inverse fashion. ACC2 hydroxylation occurs in conditions of high energy and represses fatty acid oxidation. PHD3-null mice demonstrate loss of ACC2 hydroxylation in heart and skeletal muscle and display elevated fatty acid oxidation. Whole body or skeletal muscle-specific PHD3 loss enhances exercise capacity during an endurance exercise challenge. In sum, these data identify an unexpected link between AMPK and PHD3, and a role for PHD3 in acute exercise endurance capacity and skeletal muscle metabolism.

Indexed as

Acetyl-CoA CarboxylaseAnimalsCell LineExercise ToleranceFatsFemaleHumansHypoxia-Inducible Factor-Proline DioxygenasesMaleMiceMice, Inbred C57BLMice, KnockoutMice, TransgenicMuscle, SkeletalOxidation-ReductionACACB protein, humanAcacb protein, mouseAcetyl-CoA CarboxylaseEGLN3 protein, humanFatsHypoxia-Inducible Factor-Proline Dioxygenasesacetyl-CoA carboxylase 2 modificationexercise capacityfat catabolismProlyl hydroxylase 3

Identifiers

PMID32663458
PMCPMC8065255
OpenAlexW3040832221

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.