Evidence map›Paper›PMID 41381735›Full record

ArticleEMBO reports2026

Conserved lipid metabolic reprogramming confers hypoxic and aging resilience.

Wei I Jiang, Goncalo Dias do Vale, Quentinn Pearce, Kaitlyn Kong, Wenbin Zhou, Jeffrey G McDonald, James E Cox, Neel S Singhal, Dengke K Ma

Abstract read
In one paragraph

Article in EMBO reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Wei I JiangCardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA.ORCID 0000-0002-6394-635X
Goncalo Dias do ValeCenter for Human Nutrition and Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, USA.ORCID 0000-0003-1104-0289
Quentinn PearceMetabolomics Core Research Facility, University of Utah, Salt Lake City, UT, USA.
Kaitlyn KongCardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA.
Wenbin ZhouCardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA.
Jeffrey G McDonaldCenter for Human Nutrition and Department of Molecular Genetics, University of Texas Southwestern Medical Center, Dallas, USA.ORCID 0000-0003-1570-4142
James E CoxMetabolomics Core Research Facility, University of Utah, Salt Lake City, UT, USA.
Neel S SinghalDepartment of Neurology, University of California San Francisco, San Francisco, USA.ORCID 0000-0003-1605-4444
Dengke K MaCardiovascular Research Institute, University of California San Francisco, San Francisco, CA, USA. Dengke.Ma@ucsf.edu.ORCID 0000-0002-5619-7485

Funding

WormBase: a core data resource for C. elegans and other nematodesU24HG002223 · NHGRI · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI TIM SCHEDL, PAUL Warren STERNBERG · 2018 to 2026
$18.9M
Center for C elegans AnatomyR24OD010943 · OD · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI DAVID H. HALL, Nathan Schroeder · 2012 to 2026
$9.6M
Enhancing and expanding the CGC Strain CollectionP40OD010440 · OD · UNIVERSITY OF MINNESOTA · PI Aric L Daul, Ann E. Rougvie · 2012 to 2026
$7.5M
UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeffrey M Zigman · 2022 to 2026
$7.4M
Genetic pathway and cellular mechanism underlying organismic responses to hypoxia and hypothermiaR35GM139618 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI Dengke Ma · 2021 to 2026
$2.3M
Agilent 6550 QTOF system for U of UtahS10OD016232 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2013 to 2013
$578k
Q-ToF Mass Spectrometer for the University of Utah MS and Proteomics CoreS10OD018210 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2015 to 2015
$530k
Agilent 7200 GC/Q-TOF for the University of UtahS10OD021505 · OD · UNIVERSITY OF UTAH · PI COX, JAMES ERIC · 2016 to 2016
$401k
HHS | NIH | National Institute of General Medical Sciences (NIGMS) R35GM139618NHGRI NIH HHS U24 HG002223NIDDK NIH HHS P30 DK127984NIGMS NIH HHS R35 GM139618NIH HHS P40 OD010440NIH HHS R24 OD010943NIH HHS S10 OD016232NIH HHS S10 OD018210NIH HHS S10 OD021505
6 · The paper itself

Abstract

The Arctic ground squirrel (AGS, Urocitellus parryii), an extreme hibernator, exhibits remarkable resilience to stressors like hypoxia and hypothermia, making it an ideal model for studying cellular metabolic adaptation. The underlying mechanisms of AGS resilience are largely unknown. Here, we use lipidomic and metabolomic profiling to discover specific downregulation of triglyceride lipids and upregulation of the lipid biosynthetic precursor malonic acid in AGS neural stem cells (NSC) versus murine NSCs. Inhibiting lipid biosynthesis recapitulates hypoxic resilience of squirrel NSCs. Extending this model, we find that acute exposure to hypoxia downregulates key lipid biosynthetic enzymes in C. elegans, while inhibiting lipid biosynthesis reduces mitochondrial fission and facilitates hypoxic survival. Moreover, inhibiting lipid biosynthesis protects against APOE4-induced pathologies and aging trajectories in C. elegans. These findings suggest triglyceride downregulation as a conserved metabolic resilience mechanism, offering insights into protective strategies for neural tissues under hypoxic or ischemic conditions, APOE4-induced pathologies and aging.

Indexed as

AgingHypoxiaLipid MetabolismAnimalsCaenorhabditis elegansMetabolic ReprogrammingMiceMitochondrial DynamicsNeural Stem CellsTriglyceridesTriglyceridesArctic Ground SquirrelC. elegansHypoxiaLipid Biosynthetic EnzymesTriglyceride Lipids

Identifiers

PMID41381735
PMCPMC12894929

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.