Evidence map›Paper›PMID 24969109›Full record

ArticleDiabetes2014

Reducing RIP140 expression in macrophage alters ATM infiltration, facilitates white adipose tissue browning, and prevents high-fat diet-induced insulin resistance.

Pu-Ste Liu, Yi-Wei Lin, Bomi Lee, Shelly K McCrady-Spitzer, James A Levine, Li-Na Wei

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed
6.9field-weighted citation impact, top 3% 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

29 citing papers in PubMed, 54 citations in OpenAlex.

  1. Nuclear receptor coregulator NRIP1 R448G modulates T cell gut homing to control intestinal inflammation.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  2. Review
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  5. Spinophilin-deficient mice are protected from diet-induced obesity and insulin resistance.American journal of physiology. Endocrinology and metabolism · 2020
    Article
  6. Review
  7. Article
  8. Immunometabolism features of metabolic deregulation and cancer.Journal of cellular and molecular medicine · 2019
    Review
  9. Article
  10. Article
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  13. Article
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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

6 authors at 2 institutions in 1 country.

Pu-Ste LiuDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, MN.
Yi-Wei LinDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, MN.
Bomi LeeDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, MN.
Shelly K McCrady-SpitzerEndocrine Research Unit, Mayo Clinic, Rochester, MN.
James A LevineEndocrine Research Unit, Mayo Clinic, Rochester, MN.
Li-Na WeiDepartment of Pharmacology, University of Minnesota Medical School, Minneapolis, MN weixx009@umn.edu.
University of Minnesota Medical Center · USMayo Clinic in Florida · US

Funding

Obesity and Energy Metabolism CoreP30DK050456 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI CROW, SCOTT J · 1995 to 2015
$17.0M
Studies of nuclear receptor corepressor, NRIP1, in vitamin A signaling pathwaysR01DK060521 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI WEI, LI-NA · 2002 to 2022
$6.9M
TR2 NUCLEAR RECEPTOR IN VITAMIN A SIGNALING PATHWAYSR01DK054733 · NIDDK · UNIVERSITY OF MINNESOTA TWIN CITIES · PI WEI, LI-NA · 1999 to 2021
$5.7M
NIDDK NIH HHS DK-54733NIDDK NIH HHS DK-54733-11SNIDDK NIH HHS DK-60521NIDDK NIH HHS P30 DK050456NIDDK NIH HHS R01 DK054733NIDDK NIH HHS R01 DK060521
6 · The paper itself

Abstract

Adipose tissue macrophage (ATM) recruitment and activation play a critical role in obesity-induced inflammation and insulin resistance (IR). The mechanism regulating ATM activation and infiltration remains unclear. In this study, we found receptor interacting protein 140 (RIP140) can regulate the dynamics of ATM that contribute to adipose tissue remodeling. A high-fat diet (HFD) elevates RIP140 expression in macrophages. We generated mice with RIP140 knockdown in macrophages using transgenic and bone marrow transplantation procedures to blunt HFD-induced elevation in RIP140. We detected significant white adipose tissue (WAT) browning and improved systemic insulin sensitivity in these mice, particularly under an HFD feeding. These mice have decreased circulating monocyte population and altered ATM profile in WAT (a dramatic reduction in inflammatory classically activated macrophages [M1] and expansion in alternatively activated macrophages [M2]), which could improve HFD-induced IR. These studies suggest that reducing RIP140 expression in monocytes/macrophages can be a new therapeutic strategy in treating HFD-induced and inflammation-related diseases.

Indexed as

Insulin ResistanceAdaptor Proteins, Signal TransducingAdipose Tissue, BrownAdipose Tissue, WhiteAnimalsDiet, High-FatGene Knockout TechniquesMacrophage ActivationMacrophagesMiceMice, Inbred C57BLMice, TransgenicNuclear ProteinsNuclear Receptor Interacting Protein 1Adaptor Proteins, Signal TransducingNuclear ProteinsNuclear Receptor Interacting Protein 1

Identifiers

PMID24969109
PMCPMC4238008
OpenAlexW2153068906

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.