Evidence map›Paper›PMID 37408258›Full record

ArticleCells2023

PPARγ Acetylation in Adipocytes Exacerbates BAT Whitening and Worsens Age-Associated Metabolic Dysfunction.

Ying He, Ruotong Zhang, Lexiang Yu, Tarik Zahr, Xueming Li, Tae-Wan Kim, Li Qiang

Open access · goldAbstract read
In one paragraph

Article in Cells, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed, 1 pooled it
3.9field-weighted citation impact, top 6% 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

19 citing papers in PubMed, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. New Mediators in the Crosstalk between Different Adipose Tissues.International journal of molecular sciences · 2024
    Pooled it
  2. Review
  3. Article
  4. Article
  5. DHA ModulatesInternational journal of molecular sciences · 2025
    Article
  6. Review
  7. Review
  8. Review
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  10. Article
  11. Article
  12. Effects of Brown Rice, Meal Replacements, and Anti-Obesity Drugs on Mitochondria in Obese Rats.Diabetes, metabolic syndrome and obesity : targets and therapy · 2025
    Article
  13. Review
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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

7 authors at 1 institution in 1 country.

Ying HeNaomi Berrie Diabetes Center, Columbia University, New York, NY 10032, USA.
Ruotong ZhangNaomi Berrie Diabetes Center, Columbia University, New York, NY 10032, USA.
Lexiang YuNaomi Berrie Diabetes Center, Columbia University, New York, NY 10032, USA.
Tarik ZahrNaomi Berrie Diabetes Center, Columbia University, New York, NY 10032, USA.
Xueming LiStuyvesant High School, New York, NY 10032, USA.
Tae-Wan KimDepartment of Pathology and Cell Biology, Columbia University, New York, NY 10032, USA.
Li QiangNaomi Berrie Diabetes Center, Columbia University, New York, NY 10032, USA.
Columbia University · US

Funding

RESEARCH TRAININGP30DK026687 · NIDDK · ST. LUKE'S-ROOSEVELT INST FOR HLTH SCIS · PI Anthony W Ferrante, DYMPNA GALLAGHER · 1986 to 2026
$33.0M
TTC39B in obesity and atherosclerosisP01HL087123 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI TALL, ALAN RICHARD · 2007 to 2022
$31.2M
Adipsin in NASHR01DK131169 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI Utpal Pajvani · 2022 to 2026
$2.9M
Microglial TREM2 Interactome in Alzheimers DiseaseR01AG067606 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI KIM, TAE-WAN · 2020 to 2024
$2.6M
PPARgamma Deacetylation in the Restoration of Metabolic HomeostasisR01DK112943 · NIDDK · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI QIANG, LI · 2018 to 2022
$2.4M
Preclinical Validation of PPARg Acetylation Inhibitors for Diabetes Prevention and TreatmentR01DK128848 · NIDDK · UNIVERSITY OF OKLAHOMA HLTH SCIENCES CTR · PI WANG, WEIDONG · 2021 to 2025
$2.4M
NHLBI NIH HHS P01 HL087123NIA NIH HHS R01 AG067606NIDDK NIH HHS P30 DK026687NIDDK NIH HHS R01 DK112943NIDDK NIH HHS R01 DK128848NIDDK NIH HHS R01 DK131169
6 · The paper itself

Abstract

Aging and obesity are the two prominent driving forces of metabolic dysfunction, yet the common underlying mechanisms remain elusive. PPARγ, a central metabolic regulator and primary drug target combatting insulin resistance, is hyperacetylated in both aging and obesity. By employing a unique adipocyte-specific PPARγ acetylation-mimetic mutant knock-in mouse model, namely aKQ, we demonstrate that these mice develop worsened obesity, insulin resistance, dyslipidemia, and glucose intolerance as they age, and these metabolic deregulations are resistant to intervention by intermittent fasting. Interestingly, aKQ mice show a whitening phenotype of brown adipose tissue (BAT) manifested in lipid filling and suppressed BAT markers. Diet-induced obese aKQ mice retain an expected response to thiazolidinedione (TZD) treatment, while BAT function remains impaired. This BAT whitening phenotype persists even with the activation of SirT1 through resveratrol treatment. Moreover, the adverse effect of TZDs on bone loss is exacerbated in aKQ mice and is potentially mediated by their increased Adipsin levels. Our results collectively suggest pathogenic implications of adipocyte PPARγ acetylation, contributing to metabolic dysfunction in aging and thus posing as a potential therapeutic target.

Indexed as

Adipose Tissue, BrownInsulin ResistancePPAR gammaAcetylationAdipocytesAnimalsMiceObesityPPAR gammaPparg protein, mousebrown adipose tissuemetabolic dysfunctionPPARγ acetylationwhitening

Identifiers

PMID37408258
PMCPMC10217233
OpenAlexW4377103881

What OpenQuestion 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 OpenQuestion graph.