Evidence map›Paper›PMID 38062308›Full record

ArticleMolecular biomedicine2023

Apolipoprotein E (ApoE) orchestrates adipose tissue inflammation and metabolic disorders through NLRP3 inflammasome.

Yulin Zhang, Ziwei Cheng, Liyu Hong, Jia Liu, Xinyue Ma, Wenjing Wang, Ran Pan, Wenjie Lu, Qichao Luo, Shan Gao and 1 more

Abstract read
In one paragraph

Article in Molecular biomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Genes · 2025
    Review
  10. Review
  11. Article
  12. Review
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

11 authors.

Yulin Zhang *Department of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Ziwei Cheng *Department of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Liyu Hong *The Second Clinical Medical College, Anhui Medical University, Hefei, 230032, China.
Jia Liu *Department of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Xinyue MaDepartment of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Wenjing WangDepartment of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China.
Ran PanRainbowFish Rehabilitation and Nursing School, Hangzhou Vocational and Technical College, Hangzhou, 310000, China.
Wenjie LuDepartment of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China. wenjie63136@163.com.
Qichao LuoDepartment of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China. luoqichao@ahmu.edu.cn.
Shan GaoDepartment of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China. aydgs@126.com.
Qin KongDepartment of Pharmacology, School of Basic Medical Sciences, Anhui Medical University, Hefei, 230032, China. kongqin@ahmu.edu.cn.ORCID http://orcid.org/0000-0002-1969-479X

Funding

Anhui Medical University Research Enhancement Program Funding Project 2022xkjT001Anhui Provincial University Natural Science Foundation Key Project KJ2020A0149, 2023AH050670National College Students Innovation and Entrepreneurship Training Program S202210366043, S202210366020, and S202310366061
6 · The paper itself

Abstract

Obesity is a metabolic disorder characterized by the hypertrophy expansion of adipose tissue, resulting in dysregulated energy metabolism, and accompanied by chronic low-grade inflammation. Adipose tissue macrophages (ATMs), a principal component of inflammation, respond to microenvironment signals and modulate adipose tissue remodeling and metabolic processes situation-specific. However, the mechanisms governing how the organism maintains equilibrium between its chronic inflammation and metabolism still need to be understood. Here, we describe a novel role of apolipoprotein E (ApoE), which associated with lipid particles, in maintaining fat deposition and system metabolic inflammation. Using human samples and mouse models, we show that ApoE is robustly downregulated in obese individuals, db/db mice, and mice of high-fat diet (HFD) feeding and increased in obese subjects with diabetes. Furthermore, we found that ApoE deficiency mice globally prevented obesity by restraining adipose tissue expansion and improved systemic glucose tolerance and insulin sensitivity. However, macrophage contributed to metabolic inflammation due to increased IL-1β production in adipose tissue from ApoE

Indexed as

Adipose tissueApolipoprotein E (ApoE)MacrophageMetabolic inflammationNOD-, LRR- and Pyrin Domain-Containing Protein 3 (NLRP3)

Identifiers

PMID38062308
PMCPMC10703753

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Registered trials

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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.