Evidence map›Paper›PMID 38332049›Full record

ArticleCell death and differentiation2024

ACSS2 controls PPARγ activity homeostasis to potentiate adipose-tissue plasticity.

Nuo Chen, Ming Zhao, Nan Wu, Yaxin Guo, Baihui Cao, Bing Zhan, Yubin Li, Tian Zhou, Faliang Zhu, Chun Guo and 4 more

Open access · hybridAbstract read
In one paragraph

Article in Cell death and differentiation, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

16 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Gabpα-Pparγ Complex Determines Glycolytic Capacity and Lactic Acid Homeostasis in Brown Fat.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Article
  15. Review
  16. Article
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

14 authors at 1 institution in 1 country.

Nuo Chen *Department of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Ming Zhao *Department of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Nan WuDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Yaxin GuoDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Baihui CaoDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Bing ZhanDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Yubin LiDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Tian ZhouDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Faliang ZhuDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Chun GuoDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.
Yongyu ShiDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.ORCID 0000-0003-1356-3219
Qun WangDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China.ORCID 0000-0002-2841-2651
Yan LiDepartment of Pathogen Biology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China. liyan2015@sdu.edu.cn.
Lining ZhangDepartment of Immunology, School of Basic Medical Science, Cheeloo College of Medicine, Shandong University, Jinan, China. zhanglining@sdu.edu.cn.ORCID 0000-0002-8977-1148
Shandong University · CN

Funding

National Natural Science Foundation of China (National Science Foundation of China) 81771775National Natural Science Foundation of China (National Science Foundation of China) 81971471National Natural Science Foundation of China (National Science Foundation of China) 82101606National Natural Science Foundation of China (National Science Foundation of China) 82173105National Natural Science Foundation of China (National Science Foundation of China) 82270605
6 · The paper itself

Abstract

The appropriate transcriptional activity of PPARγ is indispensable for controlling inflammation, tumor and obesity. Therefore, the identification of key switch that couples PPARγ activation with degradation to sustain its activity homeostasis is extremely important. Unexpectedly, we here show that acetyl-CoA synthetase short-chain family member 2 (ACSS2) critically controls PPARγ activity homeostasis via SIRT1 to enhance adipose plasticity via promoting white adipose tissues beiging and brown adipose tissues thermogenesis. Mechanistically, ACSS2 binds directly acetylated PPARγ in the presence of ligand and recruits SIRT1 and PRDM16 to activate UCP1 expression. In turn, SIRT1 triggers ACSS2 translocation from deacetylated PPARγ to P300 and thereafter induces PPARγ polyubiquitination and degradation. Interestingly, D-mannose rapidly activates ACSS2-PPARγ-UCP1 axis to resist high fat diet induced obesity in mice. We thus reveal a novel ACSS2 function in coupling PPARγ activation with degradation via SIRT1 and suggest D-mannose as a novel adipose plasticity regulator via ACSS2 to prevent obesity.

Indexed as

HomeostasisPPAR gammaSirtuin 1Acetate-CoA LigaseAdipose TissueAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsDiet, High-FatDNA-Binding ProteinsHumansMaleMannoseMiceMice, Inbred C57BLObesityAcetate-CoA LigaseDNA-Binding ProteinsMannosePPAR gammaPrdm16 protein, mouseSirt1 protein, mouseSirtuin 1Transcription FactorsUncoupling Protein 1

Identifiers

PMID38332049
PMCPMC11043345
OpenAlexW4391652704

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.