Evidence map›Paper›PMID 34162682›Full record

ArticleDiabetes2021

Adiponectin Alleviates Diet-Induced Inflammation in the Liver by Suppressing MCP-1 Expression and Macrophage Infiltration.

Jiyoon Ryu, Jason T Hadley, Zhi Li, Feng Dong, Huan Xu, Xiaoban Xin, Ye Zhang, Cang Chen, Senlin Li, Xiaoning Guo and 7 more

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 2 pooled it
9.0field-weighted citation impact, top 1% 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

30 citing papers in PubMed, 2 syntheses or guidelines pooled it, 74 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Review
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  7. Review
  8. Adipokine in Metabolic Liver Disease: Adipo-Brain-Liver Cross talk.International journal of endocrinology · 2026
    Review
  9. Review
  10. Review
  11. Article
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  14. Article
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  17. Metabolic dysfunction-associated fatty liver disease and osteoporosis: the mechanisms and roles of adiposity.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2024
    Review
  18. Lack ofGenes · 2024
    Article
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  20. 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

17 authors at 1 institution in 1 country.

Jiyoon RyuDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Jason T HadleyDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Zhi LiDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Feng DongDepartment of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Huan XuDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Xiaoban XinDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Ye ZhangDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Cang ChenDepartment of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Senlin LiDepartment of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Xiaoning GuoDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Jared L ZhaoDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Robin J LeachDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Muhammad A Abdul-GhaniDepartment of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX.ORCID 0000-0003-4556-1787
Ralph A DeFronzoDepartment of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX.ORCID 0000-0002-8581-6273
Amrita KamatDepartment of Medicine, University of Texas Health Science Center at San Antonio, San Antonio, TX.
Feng LiuDepartment of Pharmacology, University of Texas Health Science Center at San Antonio, San Antonio, TX.ORCID 0000-0002-5098-1711
Lily Q DongDepartment of Cell Systems and Anatomy, University of Texas Health Science Center at San Antonio, San Antonio, TX dongq@uthscsa.edu.ORCID 0000-0002-6293-818X
The University of Texas Health Science Center at San Antonio · US

Funding

TRANSGENIC COREP30AG013319 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI PETER J HORNSBY · 1995 to 2026
$30.6M
TRAINING GRANT ON THE BIOLOGY OF AGINGT32AG021890 · NIA · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI Erzsebet Kokovay, JAMES FLOYD NELSON · 2003 to 2026
$11.4M
The role of TCTP in regulating adiponectin signalingR01DK102965 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI DONG, LILY Q · 2015 to 2019
$1.7M
Regulation of Mitochondrial Biogenesis and Function by DsbA-L in the LiverR01DK114479 · NIDDK · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI FRAZER, ALAN · 2018 to 2021
$1.4M
NIA NIH HHS P30 AG013319NIA NIH HHS T32 AG021890NIDDK NIH HHS R01 DK102965NIDDK NIH HHS R01 DK114479
6 · The paper itself

Abstract

Adiponectin is an adipokine that exerts insulin-sensitizing and anti-inflammatory roles in insulin target tissues including liver. While the insulin-sensitizing function of adiponectin has been extensively investigated, the precise mechanism by which adiponectin alleviates diet-induced hepatic inflammation remains elusive. Here, we report that hepatocyte-specific knockout (KO) of the adaptor protein APPL2 enhanced adiponectin sensitivity and prevented mice from developing high-fat diet-induced inflammation, insulin resistance, and glucose intolerance, although it caused fatty liver. The improved anti-inflammatory and insulin-sensitizing effects in the APPL2 hepatocyte-specific KO mice were largely reversed by knocking out adiponectin. Mechanistically, hepatocyte APPL2 deficiency enhances adiponectin signaling in the liver, which blocks TNF-α-stimulated MCP-1 expression via inhibiting the mTORC1 signaling pathway, leading to reduced macrophage infiltration and thus reduced inflammation in the liver. With results taken together, our study uncovers a mechanism underlying the anti-inflammatory role of adiponectin in the liver and reveals the hepatic APPL2-mTORC1-MCP-1 axis as a potential target for treating overnutrition-induced inflammation in the liver.

Indexed as

Adaptor Proteins, Signal TransducingAdiponectinAnimalsCell MovementChemokine CCL2Diet, High-FatDown-RegulationFatty LiverHepatitisHepatocytesInflammationInsulin ResistanceLiverMacrophagesMaleMiceAdaptor Proteins, Signal TransducingAdiponectinCcl2 protein, mouseChemokine CCL2DCC-interacting protein 13-beta, mouse

Identifiers

PMID34162682
PMCPMC8275886
OpenAlexW3136514165

What OpenQuestion holds

Textmetadata
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.